WO2008077147A2 - Devices, systems, methods and tools for continuous glucose monitoring - Google Patents
Devices, systems, methods and tools for continuous glucose monitoring Download PDFInfo
- Publication number
- WO2008077147A2 WO2008077147A2 PCT/US2007/088456 US2007088456W WO2008077147A2 WO 2008077147 A2 WO2008077147 A2 WO 2008077147A2 US 2007088456 W US2007088456 W US 2007088456W WO 2008077147 A2 WO2008077147 A2 WO 2008077147A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- glucose
- monitor
- sensing
- fluid
- sensor
- Prior art date
Links
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 title claims abstract description 352
- 239000008103 glucose Substances 0.000 title claims abstract description 352
- 238000000034 method Methods 0.000 title claims abstract description 60
- 238000012544 monitoring process Methods 0.000 title claims abstract description 26
- 210000001519 tissue Anatomy 0.000 claims abstract description 85
- 239000000758 substrate Substances 0.000 claims abstract description 73
- 210000003722 extracellular fluid Anatomy 0.000 claims abstract description 40
- 210000000434 stratum corneum Anatomy 0.000 claims abstract description 16
- 210000002615 epidermis Anatomy 0.000 claims abstract description 4
- 239000012530 fluid Substances 0.000 claims description 179
- 210000003491 skin Anatomy 0.000 claims description 38
- 238000004891 communication Methods 0.000 claims description 35
- 210000004369 blood Anatomy 0.000 claims description 29
- 239000008280 blood Substances 0.000 claims description 29
- 230000036760 body temperature Effects 0.000 claims description 25
- 239000002699 waste material Substances 0.000 claims description 21
- 239000000853 adhesive Substances 0.000 claims description 14
- 230000001070 adhesive effect Effects 0.000 claims description 14
- 229910052751 metal Inorganic materials 0.000 claims description 13
- 239000002184 metal Substances 0.000 claims description 13
- 229910045601 alloy Inorganic materials 0.000 claims description 8
- 239000000956 alloy Substances 0.000 claims description 8
- 239000010935 stainless steel Substances 0.000 claims description 6
- 229910001220 stainless steel Inorganic materials 0.000 claims description 6
- 238000001727 in vivo Methods 0.000 claims description 3
- CCEKAJIANROZEO-UHFFFAOYSA-N sulfluramid Chemical group CCNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F CCEKAJIANROZEO-UHFFFAOYSA-N 0.000 claims description 2
- 238000009792 diffusion process Methods 0.000 abstract description 8
- 108090000790 Enzymes Proteins 0.000 description 13
- 102000004190 Enzymes Human genes 0.000 description 13
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 13
- 206010012601 diabetes mellitus Diseases 0.000 description 13
- 229940088598 enzyme Drugs 0.000 description 13
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 12
- 239000003153 chemical reaction reagent Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 108010015776 Glucose oxidase Proteins 0.000 description 8
- 235000019420 glucose oxidase Nutrition 0.000 description 8
- 230000035515 penetration Effects 0.000 description 8
- 239000004366 Glucose oxidase Substances 0.000 description 7
- 239000012491 analyte Substances 0.000 description 7
- 229940116332 glucose oxidase Drugs 0.000 description 7
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 7
- 102000004877 Insulin Human genes 0.000 description 6
- 108090001061 Insulin Proteins 0.000 description 6
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 6
- 229940125396 insulin Drugs 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 238000001514 detection method Methods 0.000 description 5
- YAGKRVSRTSUGEY-UHFFFAOYSA-N ferricyanide Chemical compound [Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] YAGKRVSRTSUGEY-UHFFFAOYSA-N 0.000 description 5
- 230000036541 health Effects 0.000 description 5
- 238000012806 monitoring device Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 238000004364 calculation method Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000004020 conductor Substances 0.000 description 4
- 235000012054 meals Nutrition 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 230000035945 sensitivity Effects 0.000 description 4
- 208000001072 type 2 diabetes mellitus Diseases 0.000 description 4
- 229910021607 Silver chloride Inorganic materials 0.000 description 3
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 3
- 238000011088 calibration curve Methods 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 238000006056 electrooxidation reaction Methods 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 2
- 229910000906 Bronze Inorganic materials 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- 206010022489 Insulin Resistance Diseases 0.000 description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000010951 brass Substances 0.000 description 2
- 239000010974 bronze Substances 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 2
- 230000002596 correlated effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000005553 drilling Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- -1 etc.) Substances 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 229910052732 germanium Inorganic materials 0.000 description 2
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 230000003914 insulin secretion Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910052762 osmium Inorganic materials 0.000 description 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 2
- 230000036284 oxygen consumption Effects 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 229910052703 rhodium Inorganic materials 0.000 description 2
- 239000010948 rhodium Substances 0.000 description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 2
- 229910052707 ruthenium Inorganic materials 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 210000002966 serum Anatomy 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 229910052715 tantalum Inorganic materials 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 201000004569 Blindness Diseases 0.000 description 1
- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical compound OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 description 1
- 108010050375 Glucose 1-Dehydrogenase Proteins 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 150000000996 L-ascorbic acids Chemical class 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 206010033307 Overweight Diseases 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 208000018262 Peripheral vascular disease Diseases 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- 238000002679 ablation Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 206010003246 arthritis Diseases 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 239000012472 biological sample Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000004397 blinking Effects 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 238000013130 cardiovascular surgery Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 208000029078 coronary artery disease Diseases 0.000 description 1
- 230000000875 corresponding effect Effects 0.000 description 1
- 238000003869 coulometry Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000012502 diagnostic product Substances 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 210000000245 forearm Anatomy 0.000 description 1
- 235000012209 glucono delta-lactone Nutrition 0.000 description 1
- 229960003681 gluconolactone Drugs 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 239000000017 hydrogel Substances 0.000 description 1
- 201000001421 hyperglycemia Diseases 0.000 description 1
- 230000028993 immune response Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 230000006362 insulin response pathway Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 238000003698 laser cutting Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 238000001020 plasma etching Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001690 polydopamine Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920000307 polymer substrate Polymers 0.000 description 1
- 229910001414 potassium ion Inorganic materials 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 208000035408 type 1 diabetes mellitus 1 Diseases 0.000 description 1
- 150000007968 uric acids Chemical class 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000000707 wrist Anatomy 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
- A61B5/14532—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue for measuring glucose, e.g. by tissue impedance measurement
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
- A61B5/14507—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue specially adapted for measuring characteristics of body fluids other than blood
- A61B5/1451—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue specially adapted for measuring characteristics of body fluids other than blood for interstitial fluid
- A61B5/14514—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue specially adapted for measuring characteristics of body fluids other than blood for interstitial fluid using means for aiding extraction of interstitial fluid, e.g. microneedles or suction
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
- A61B5/1486—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using enzyme electrodes, e.g. with immobilised oxidase
- A61B5/14865—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using enzyme electrodes, e.g. with immobilised oxidase invasive, e.g. introduced into the body by a catheter or needle or using implanted sensors
Definitions
- the invention relates to systems, devices, and tools, and the use of such systems, devices and tools for monitoring blood glucose levels in a person having diabetes. More specifically, the invention relates to systems, devices, and tools and the use of such systems, devices and tools for monitoring blood glucose level continuously, or substantially continuously.
- Diabetes is a chronic, life-threatening disease for which there is no known cure. It is a syndrome characterized by hyperglycemia and relative insulin deficiency. Diabetes affects more than 120 million people world wide, and is projected to affect more than 220 million people by the year 2020. It is estimated that one out of every three children today will develop diabetes sometime during their lifetime. Diabetes is usually irreversible, and can lead to a variety of severe health complications, including coronary artery disease, peripheral vascular disease, blindness and stroke. The Center for Disease Control (CDC) has reported that there is a strong association between being overweight, obesity, diabetes, high blood pressure, high cholesterol, asthma and arthritis. Individuals with a body mass index of 40 or higher are more than 7 times more likely to be diagnosed with diabetes.
- CDC Center for Disease Control
- Type I diabetes insulin-dependent diabetes mellitus
- Type II diabetes non-insulin-dependent diabetes mellitus
- Varying degrees of insulin secretory failure may be present in both forms of diabetes.
- diabetes is also characterized by insulin resistance. Insulin is the key hormone used in the storage and release of energy from food.
- the insulin response does not function properly (either due to inadequate levels of insulin production or insulin resistance), resulting in blood glucose levels below 80 mg/dL during fasting and well above 140 mg/dL after a meal.
- persons suffering from diabetes have limited options for treatment, including taking insulin orally or by injection. In some instances, controlling weight and diet can impact the amount of insulin required, particularly for non-insulin dependent diabetics.
- Monitoring blood glucose levels is an important process that is used to help diabetics maintain blood glucose levels as near as normal as possible throughout the day.
- the blood glucose self-monitoring market is the largest self-test market for medical diagnostic products in the world, with a size of approximately over $3 billion in the United States and $7.0 billion worldwide. It is estimated that the worldwide blood glucose self-monitoring market will amount to $9.0 billion by 2008. Failure to manage the disease properly has dire consequences for diabetics.
- the direct and indirect costs of diabetes exceed $130 billion annually in the United States - about 20% of all healthcare costs.
- Non-continuous systems consist of meters and tests strips and require blood samples to be drawn from fingertips or alternate sites, such as forearms and legs (e.g. OneTouch® Ultra by LifeScan, Inc., Milpitas, CA, a Johnson & Johnson company). These systems rely on lancing and manipulation of the fingers or alternate blood draw sites, which can be extremely painful and inconvenient, particularly for children.
- Continuous monitoring sensors are generally implanted subcutaneously and measure glucose levels in the interstitial fluid at various periods throughout the day, providing data that shows trends in glucose measurements over a short period of time. These sensors are painful during insertion and usually require the assistance of a health care professional. Further, these sensors are intended for use during only a short duration (e.g., monitoring for a matter of days to determine a blood sugar pattern). Subcutaneously implanted sensors also frequently lead to infection and immune response complications. Another major drawback of currently available continuous monitoring devices is that they require frequent, often daily, calibration using blood glucose results that must be obtained from painful finger-sticks using traditional meters and test strips. This calibration, and re-calibration, is required to maintain sensor accuracy and sensitivity, but it can be cumbersome as well as painful.
- Medtronic www.medtronic.com
- Medtronic has two continuous glucose monitoring products approved for sale: Guardian® RT Real-Time Glucose Monitoring System and CGMS® System.
- Each product includes an implantable sensor that measures and stores glucose values for a period of up to three days.
- One product is a physician product. The sensor is required to be implanted by a physician, and the results of the data aggregated by the system can only be accessed by the physician, who must extract the sensor and download the results to a personal computer for viewing using customized software.
- the other product is a consumer product, which permits the user to download results to a personal computer using customized software.
- a third product approved for continuous glucose monitoring is the Glucowatch® developed by Cygnus Inc., which is worn on the wrist like a watch and can take glucose readings every ten to twenty minutes for up to twelve hours at a time. It requires a warm up time of 2 to 3 hours and replacement of the sensor pads every 12 hours. Temperature and perspiration are also known to affect its accuracy.
- the fourth approved product is a subcutaneously implantable glucose sensor developed by Dexcom, San Diego, CA (www.dexcom.com). All of the approved devices are known to require daily, often frequent, calibrations with blood glucose values which the patient must obtain using conventional finger stick blood glucose monitors.
- One aspect of the invention is a glucose monitor including at least one substantially cylindrical tissue piercing element having a distal opening, a proximal opening, and a substantially cylindrical interior lumen extending between the distal and proximal openings, a sensing area in fluid communication with the proximal opening of the at least one substantially cylindrical tissue piercing element, sensing fluid extending from the sensing area into substantially the entire interior lumen of the at least one substantially cylindrical tissue piercing element, and a glucose sensor adapted to sense a concentration of glucose in the sensing fluid within the sensing area.
- the monitor may also include a substrate coupled to and supporting the at least one substantially cylindrical tissue piercing element.
- the substrate can include a lumen in fluid communication with the proximal opening of the tissue piercing element and the sensing area.
- the at least one tissue piercing element is made of a metal or alloy such as a stainless steel.
- the tissue piercing element may be tapered at its distal opening.
- the substantially cylindrical tissue piercing element is preferably configured to pierce only as deep as into the epidermis layer of the skin.
- the monitor also includes a sensing fluid reservoir in fluid communication with the sensing area, wherein the sensing fluid reservoir is adapted to house a reservoir of sensing fluid with a known glucose concentration.
- the glucose monitor may also include an actuator such as a pump and/or valves configured to move fresh sensing fluid from the at least one sensing fluid reservoir into the sensing area. The actuator can be automatically or manually actuated.
- the monitor may also include a waste reservoir or waste unit in fluidic communication with the sensing area adapted to receive sensing fluid from the sensing area when the fresh sensing fluid is moved into the sensing area.
- the known glucose concentration is between about 0 mg/dl and about 400 mg/dl.
- the sensing fluid reservoir is a first sensing fluid reservoir adapted to house a first sensing fluid with a first known glucose concentration
- the glucose monitor further comprising a second sensing fluid reservoir adapted to house a second sensing fluid with a second known glucose concentration, wherein the first and second known glucose concentrations are not the same.
- the first known glucose concentration is between about 0 mg/dl and about 100 mg/dl
- the second known glucose concentration is between about 100 mg/dl and about 400 mg/dl.
- the monitor includes a removable cover extending over the distal opening of the at least one substantially cylindrical tissue piercing element.
- the monitor includes a display adapted to display a glucose concentration.
- the sensor can be housed in a first housing and the display can be housed in a second housing, wherein the first housing comprises a transmitter to wirelessly transmit information indicative of the glucose concentration sensed by the sensor to a receiver in the second housing.
- the second housing can be adapted to determine the glucose concentration in the interstitial fluid and therefore the blood of the patient based on the information indicative of the glucose concentration sensed by the sensor.
- the monitor also includes an adhesive element adapted to attach the glucose monitor to the skin of a subject.
- the glucose monitor is adapted to detect a concentration of glucose in the sensing fluid with the sensing area without extracting interstitial fluid through the distal opening into the interior lumen.
- the monitor includes a temperature sensor adapted to sense the body temperature of the subject, and can also include a vibration assembly adapted to vibrate at least part of the glucose monitor to allow the at least one tissue piercing element to penetrate the stratum corneum.
- Another aspect of the invention is a method of in vivo monitoring of an individual's interstitial fluid glucose concentration.
- the method comprises inserting distal ends of at least one substantially cylindrical tissue piercing element through a stratum corneum area of the individual's skin, the at least one tissue piercing element comprising a distal opening, a proximal opening, an interior lumen extending between the distal and proximal openings, and a sensing fluid filling substantially the entire interior lumen, and sensing a glucose concentration of the sensing fluid.
- a glucose sensor senses the glucose concentration
- the method also includes calibrating the glucose sensor prior to the sensing step.
- the glucose sensor may be in fluid communication with a sensing area which is in fluid communication with the interior lumen.
- the sensing fluid can have a known glucose concentration
- calibrating the glucose sensor can include determining an output from the glucose sensor based on the known glucose concentration.
- calibrating the glucose sensor also includes moving fresh sensing fluid with a known glucose concentration into the sensing area and determining an output from the glucose sensor based on the known glucose concentration of a fresh sensing fluid.
- the sensing fluid may be moved from the sensing area as the fresh sensing fluid is moved into the sensing area.
- Calibrating can include manually or automatically actuating an actuator which moves the fresh sensing fluid into the sensing area.
- the method also include adhering the at least one tissue piercing element to the subject's skin with adhesive.
- the method also includes permitting glucose to diffuse from interstitial fluid of the subject into the sensing area without extracting interstitial fluid through the distal opening in the interior lumen.
- the method can also include sensing the subject's body temperature.
- the method can further include determining a glucose concentration of the interstitial fluid of the subject wherein the determined glucose concentration is based on the sensed glucose concentration.
- the sensed glucose concentration can be transmitted to an external device separate from the device which houses the sensor, and the external device determines the glucose concentration of the interstitial fluid.
- the determined glucose concentration of the interstitial fluid can also be displayed.
- a glucose monitor including a deformed substrate layer defining a plurality of tissue piercing elements each having a distal opening, a proximal opening and a lumen extending between the distal and proximal openings, a sensing area in fluid communication with the proximal openings of the plurality of metal tissue piercing elements, sensing fluid extending from the sensing area into substantially the entire interior space of the plurality of tissue piercing elements, and a glucose sensor adapted to detect a concentration of glucose in the sensing fluid within the sensing area.
- Figures 1 and 2 are cross-sectional schematic views of a glucose monitoring device according to one embodiment of the invention with tissue piercing elements in place on a user's skin.
- Figures 3-6 show exemplary substantially cylindrical needles of the present invention.
- Figures 7 (a) - 7(c) show a method of forming deformed substrate layer of a glucose monitor.
- Figure 8 shows a close up view of a distal opening of a tissue piercing element in a deformed substrate layer.
- Figure 9 illustrates an exemplary deformed substrate layer defining a plurality of tissue piercing elements.
- Figure 10 shows a perspective view of the optionally disposable portion of the glucose monitor.
- Figure 11 shows an exploded view of a glucose monitoring device according to another embodiment of the invention.
- Figures 12(a) and 12(b) are a schematic representative drawing of a three electrode system for use with the glucose sensor of one embodiment of this invention.
- Figures 13(a) and 13(b) are a schematic representative drawing of a two electrode system for use with the glucose sensor of one embodiment of this invention.
- Figure 14 is a cross-sectional schematic view of a portion of a glucose monitoring device according to yet another embodiment of the invention.
- Figure 15 shows a remote receiver for use with a glucose monitoring system according to yet another embodiment of the invention.
- Figure 16 shows a glucose sensor in place on a user's skin and a remote monitor for use with the sensor.
- the present invention provides a significant advance in biosensor and glucose monitoring technology: portable, painless, virtually non-invasive, self-calibrating, integrated and non-implanted sensors which continuously indicate the user's blood glucose concentration, enabling swift corrective action to be taken by the patient.
- the invention may also be used in critical care situations, such an in an intensive care unit to assist health care personnel.
- the sensor and monitor of this invention may be used to measure any other analyte as well, for example, electrolytes such as sodium or potassium ions.
- the glucose sensor can be any suitable sensor including, for example, an electrochemical sensor or an optical sensor.
- Figure 1 shows a schematic cross-section of one embodiment of the glucose monitor.
- the glucose monitor 100 has one hollow needle 102 or other tissue piercing element extending through the stratum corneum 104 of a subject into the interstitial fluid 106 beneath the stratum corneum.
- the tissue piercing element is preferably hollow and has an open distal end, with an interior that communicates with a sensing area 110 within a sensor channel 108.
- Sensing area 110 is therefore in fluid communication with interstitial fluid 106 through needle 102.
- sensing area 110 and the needle 102 are pre- filled with sensing fluid prior to the first use of the device.
- glucose diffuses from the interstitial fluid into the sensing fluid within the tissue piercing element as described below.
- FIG. 2 shows another embodiment of the glucose monitor with three (3) needles 102.
- the illustrated glucose monitors are not intended to be a limitation on the number of tissue piercing elements that can be used with a glucose monitor of the present invention.
- the glucose monitor may have one, two, three, four, or more tissue piercing elements adapted to pierce the stratum corneum.
- Figures 3 and 4 provide a side view and perspective view, respectively, of the needle shown in Figure 1.
- needle 2 engages and is coupled to a substrate or chip 6 of the glucose monitor.
- Needle 102 is substantially cylindrical in shape and has a substantially cylindrical interior lumen 4 shown in phantom which provides a channel between the distal opening 10 and the proximal opening of the needle 12.
- Substrate 6 has a substrate lumen 14 shown in phantom which is in fluid communication with the interior lumen of the needle 4 and the sensing area 8,
- Figures 5 and 6 show an alternative embodiment wherein the glucose monitor has three (3) needles 2 to pierce the stratum corneum of the skin into the interstitial fluid.
- needle or “the needle” can refer to a single needle as shown in Figures
- Figures 3-6 can also show needle or needles 2 passing through the interior of, and supported by, the substrate 6.
- the interior lumen of the needle would comprise lumen 4, lumen 14 and area 8 in Figures 3 and 5.
- the proximal opening of the needle is 15.
- a passageway can be created in substrate 6 by any method known in the art, such as, for example, etching.
- a needle can then be inserted into the formed passageway to position the needle in the position shown in Figures 3-5, such as by press fitting.
- the needle can be a commercially available hypodermic needle and may or may not have to be altered before placing through and into substrate 6.
- the tissue piercing elements are preferably made from any metal or alloy such as a stainless steel.
- Other metals of which the needle can be made are iron, brass, bronze, nickel, aluminum, chrome, titanium, platinum, gold, silver, tantalum, tungsten, iridium, palladium, rhodium, ruthenium, osmium, molybdenum, or cobalt.
- Commercially available hypodermic needles may be used in the glucose monitor, such as those manufactured by Becton Dickinson or UltiMed Incorporated.
- Exemplary tissue piercing elements and their methods of production that can be used with the present invention can be found in U.S. Patent Number 7,076,987 to Martin et al.
- a commercially available hypodermic needle may need to be adapted before use with the monitors as described herein. For example, for a desired tissue piercing element length of 1 mm, it may be necessary to shorten a commercially available hypodermic needle. Other processing steps such as, for example, laser cutting, grinding, or polishing the edges may be performed as well. If the tissue piercing element is not set at a right angle in relation to the monitor however, the length of the needle could be determined based on the degree of the angle.
- the tissue piercing element is generally substantially cylindrical in shape, as shown in Figures 3-6. While the tissue piercing elements in Figures 3-6 are shown with circular cross-sections, they are not limited to such shapes. Substantially cylindrical tissue piercing elements includes tissue piercing elements that have cross-sections that are non-circular, such as hexagonal or any other cross-sectional shape.
- the distal opening of the tissue piercing element can have a tapered cut as shown in Figures 3-6 to allow for quick and efficient penetration of the skin.
- the distal tapered end can have a variety of shape designs to allow for improved penetration, such as designs described in Patent No. 6,945,964, filed October 14, 2003.
- the needles shown in Figures 3-6 are shown at a right angle to the substrate, the needle can be coupled to the substrate or pass through the substrate to assume any number of angles in relation to the substrate.
- the needle can be at a 45 degree angle to the substrate such that the needle penetrates the skin at a 45 degree angle.
- the needles shown in Figures 3-6 are substantially straight.
- the needles may have a different shape such as a curved shape to allow for easier penetration in the skin.
- the needles may have varying lengths to allow for easier penetration into the skin.
- a commercial hypodermic needle is generally available in a variety of gauges ranging from, for example, 7 to 35, but a hypodermic needle with a larger or smaller gauge number can be used. Generally, a small diameter is preferred to minimize the pain a patient will feel, however, a diameter that is too small may not provide enough structural support to penetrate the stratum corneum.
- the needle can be about 28 to about 32 gauge (i.e., about 0.36 millimeters outside diameter to about 0.23 millimeters outside diameter). In other embodiments the gauge can be about 35 or smaller. Any other gauge/diameter needle may be used in the glucose monitor of the present invention.
- the length of the tissue piercing element is preferably long enough to pierce the stratum corneum and come into contact with the interstitial fluid such that glucose from the interstitial fluid can diffuse through the needle as described below.
- Commercially available hypodermic needle can be coupled directly on the glucose monitor or through it, or can first be altered such as shortening the length to achieve a desirable length before engaging with the glucose monitor.
- Suitable materials for the substrate include but are not limited to metals, alloys such as a stainless steel, plastic, silicon, germanium, minerals (e.g. quartz), semiconducting materials (e.g. silicon, germanium, etc.), ceramic, polymers and plastic. While the substrates as shown are in a generally rectangular shape, the substrate can be in any other shape or size as may be desirable to orient the substrate in the glucose monitor.
- a substrate lumen is shown in Figures 3-6 which can fluidly connect the interior lumen of the needle with the sensing area. The substrate lumen need not always be present and the interior lumen of the needle can be in direct fluid communication with the sensing area.
- the sensing area is shown in Figures 3-6, however the sensing area need not be located inside the substrate but can be in a separate channel above the substrate (not shown in Figures 3-6), shown as sensing area 208 in Figure 10 described below.
- Fabrication of a lumen in the substrate and/or the sensing area in the substrate, such as lumen 14 and sensing area 10 in Figures 3-6 can be achieved by, for example, without limitation, a fabrication method including dry plasma etching, wet aqueous etching, water jet drilling, solid particles ablation and photon or electron beam drilling.
- the tissue piercing element can be a separate component from the substrate and can be attached to the substrate by an adhesive, glue, or other bonding technique such that the substrate lumen formed in the substrate aligns with the interior space of the needle to create a lumen extending from the distal opening of the needle to the sensing area through which the glucose can diffuse.
- a glucose monitor that comprises a deformed substrate layer defining a plurality of tissue piercing elements.
- Each of the tissue piercing elements has a distal opening, a proximal opening and a lumen or channel extending between the distal and proximal openings.
- the tissue piercing elements are preferably protrusions which are integrated with and extend from one side of the substrate.
- FIGS 7(a) - 7(c) are sectional views which show an exemplary method of producing the deformed substrate layer.
- Substrate actuator 70 comprises a plurality of pins or extensions 71 which extend from the base of substrate actuator 73.
- Substrate 72 is positioned below the substrate actuator 70.
- Substrate actuator 70 is lowered, in Figure 7(b), such that pins 71 engage and puncture substrate 72 creating distal openings 75.
- Substrate actuator 70 is then returned to its initial position in Figure 7(c), providing deformed substrate layer 77 defining tissue piercing elements 74.
- FIG 9 illustrates an exemplary deformed substrate layer with an array of tissue piercing elements 74 with distal openings 75 and deformed substrate layer 77.
- the tissue piercing elements in this embodiment can be analogized to the rough protrusions of a cheese grater.
- the substrate actuator piercing through the substrate can be analogized to a pin puncturing a sheet of aluminum foil.
- Figures 7 and 8 illustrate one shape the tissue piercing elements can assume based on the shape and design of the pin used to puncture the substrate.
- the tissue piercing elements have a general volcano shape, broader at their proximal end than at the distal end. The shape of the tissue piercing element will generally depend on the size and shape of the actuator pins.
- the substrate actuator is a steel dye but can be any material capable of piercing through the substrate and create the distal openings.
- the dye can have steel pins extending therefrom.
- the substrate is preferably a metal sheet that can be made of any metal or alloy such as a stainless steel.
- Other exemplary metals that can be used alone or in combination are iron, brass, bronze, nickel, aluminum, chrome, titanium, platinum, gold, silver, tantalum, tungsten, indium, palladium, rhodium, ruthenium, and osmium.
- the metal sheet is preferably of a thickness and strength such that the tissue piercing elements embedded therein are capable of piercing the stratum corneum of the skin to allow for glucose to diffuse through the distal opening of the tissue piercing elements.
- a deformed substrate layer can be configured to be disposed in the glucose monitor in the same or similar position as the tissue piercing elements in Figure 3-6. The deformed substrate layer could be in the same position as the substrate such that the distal opening would be in fluid communication with sensing area.
- glucose sensor is an electrochemical glucose sensor that generates an electrical signal (current, voltage or charge) whose value depends on the concentration of glucose in the fluid within sensing area 110. Details of the operation of glucose sensor 112 are discussed below.
- Sensor electronics element 114 is configured to receive an electrical signal from sensor 112. In some embodiments, sensor electronics element 114 uses the electrical signal to compute a glucose concentration and display it. In other embodiments, sensor electronics element 114 receives and transmits the electrical signal, or information derived from the electrical signal, to a remote device, such as through wireless communication. Electronics element 114 can comprise other circuitry such as an amplifier and an A/D converter which can amplify the electrical signal from the sensor and convert the amplified electrical signal to a digital signal before, for example, determining a glucose concentration or transmitting the digital signal to an external device which can then determine a glucose concentration. [0071] Glucose monitor 100 can be held in place on the skin 104 by one or more adhesive pads 116.
- Glucose monitor 100 has a novel built-in sensor calibration system.
- a sensing fluid reservoir 118 contains a sensing fluid having, e.g., a known glucose concentration between about 0 and about 400 mg/dl.
- the glucose concentration in the sensing fluid is selected to be below the glucose sensing range of the sensor.
- the sensing fluid may also contain buffers, preservatives or other components in addition to the glucose.
- a check valve 122 such as a flap valve
- any sensing fluid within channel 108 is forced through a second check valve 124 (e.g., a flap valve) into a waste reservoir 126.
- Check valves or similar gating systems are used to prevent contamination.
- sensor 112 can be calibrated at this value to set a base line. After calibration, the sensing fluid in channel 108 remains stationary, and glucose from the interstitial fluid 106 diffuses through needle 102 into the sensing area 110. Changes in the glucose concentration over time reflect differences between the calibration glucose concentration of the sensing fluid in the sensing fluid reservoir 118 and the glucose concentration of the interstitial fluid, which can be correlated with the actual blood glucose concentration of the user using proprietary algorithms. Because of possible degradation of the sensor or loss of sensor sensitivity over time, the device may be periodically recalibrated by operating actuator 120 manually or automatically to send fresh sensing fluid from sensing fluid reservoir 118 into sensing area 110.
- a glucose monitor with two or more sensing fluid reservoirs can be calibrated at one or more different glucose concentrations, which can provide a more accurate calibration curve, which can therefore provide for a more accurate glucose concentration calculation.
- FIG. 10 shows a perspective view of the optionally disposable portion of the glucose monitor.
- Housing 60 includes a fluidic network in which a plurality of reservoirs and channels are in fluid communication to allow for the movement of sensing fluid (or calibration fluid) from at least one sensing fluid reservoir through a sensing area and into at least one waste reservoir.
- Housing 60 is coupled to seal 62 which is coupled to substrate or chip 64 which comprises at least one tissue piercing element 66.
- housing 60 includes sensing fluid reservoirs 50 in fluid communication with sensing fluid channels 52, which are adapted to receive sensing fluid from the sensing fluid reservoirs.
- Sensing fluid channels 52 are in fluid communication with sensing area or sensing channel 54.
- Sensing area 54 is connected to waste channel 56, which is in fluid communication with waste reservoir 58.
- the at least one tissue piercing element 66 is in fluid communication with sensing area 54.
- a pump and/or series of valves can be incorporated into the glucose monitor to provide for the flow of fluid from the sensing fluid reservoirs to the waste reservoir.
- an actuator which can be manually or automatically actuated and work in tandem with a pump and/or series of valves to initiate the flow of fluid from the sensing fluid reservoirs.
- Waste reservoirs may be or include an absorption device such as a diaper-like material to absorb waste fluids.
- the waste reservoir may not necessarily be an enclosed structure, but may simply be an absorptive material in fluid communication with the sensing area so that it can absorb waste fluids as they are moved from the sensing area.
- Incorporating a plurality of sensing fluid reservoirs into the glucose monitor, as shown in Figure 10, allows for a multiple point calibration curve to be generated during the glucose sensor calibration, which can provide a more accurate glucose concentration calculation.
- the sensing fluids in each of the different sensing fluid reservoirs can have different known glucose concentrations, enabling the glucose sensor to be calibrated at more than one calibration point, hi general, the more calibration points that can be used to generate a relationship between the concentration of sensed glucose in the sensing area and the glucose sensor output, the more accurate the results of the glucose concentration in the interstitial fluid, and therefore the blood, may be.
- a first sensing fluid has a glucose concentration of between about 0 mg/dl and about 100 mg/dl
- a second sensing fluid has a glucose concentration of between about 100 mg/dl and about 400 mg/dl.
- the sensing fluids in each reservoir may, however, have substantially the same glucose concentration.
- the glucose monitor may be manually actuated to initiate the calibrating procedure, the glucose monitor can also be self-calibrating or self- actuating.
- the glucose monitor can include a programmable component, such as a timer, that is programmed to automatically activate a pump and valve system to initiate the flow of fresh sensing fluid from any of the sensing fluid reservoirs into the sensing area.
- the timer can be preprogrammed, or in some embodiments the monitor includes a first housing to be worn on the skin which includes the sensor and a second housing that is separate from the first housing that can display a glucose concentration.
- the second housing can be adapted such that it can program the programmable component in the first housing.
- the first housing can include a timer that can be wirelessly programmed or reprogrammed by the patient using the second housing's user interface to start the calibration at certain times.
- the method includes calibrating the glucose sensor with a plurality of different sensing fluids, which may have different concentrations of glucose.
- a first sensing fluid of known glucose concentration can either be moved into the sensing area upon manufacture of the glucose monitor, or can be moved from a sensing fluid reservoir into the sensing area before the glucose monitor is first used.
- An output from the glucose sensor is detected by the electronics element and associated with the first known glucose concentration. Any actuating technique described herein may be used to move a second sensing fluid with a second known concentration from a second sensing fluid reservoir into the sensing area, forcing the first sensing fluid into the waste reservoir.
- the output from the glucose sensor can then be similarly detected by the electronics element and associated with the second known glucose concentration.
- a calibration curve or plot can be computed to relate glucose concentration to glucose sensor output, which can then be used to determine glucose concentration of the glucose that diffuses into the sensing area from the interstitial fluid. Any number of sensing fluids, and thus calibration points, can be used to calibrate the glucose sensor. The calibrated sensor is then ready to sense a glucose concentration in the sensing area.
- the fluid with the lower glucose concentration such as a first concentration between about 0 mg/dl and 100 mg/dl
- At least one finger-stick calibration may optionally be performed or may be required to be performed at any point during the use of the monitors as described herein.
- the glucose monitor includes a body temperature sensor.
- the body temperature sensor is adapted to detect the temperature of the body of the subject.
- the glucose sensor senses a concentration of glucose in the sensing fluid within the sensing area.
- the concentration of glucose in the sensing fluid depends on the rate of diffusion of glucose molecules between the interstitial fluid in the subject and the sensing fluid in the sensing area. Diffusion is temperature dependent and as such the rate of the diffusion of glucose molecules between the interstitial fluid and the sensing fluid in the sensing area may depend on the body temperature of the subject.
- the rate of diffusion may increase as the body temperature increases, and may similarly decrease as the body temperature decreases. For example, a higher than normal body temperature can result in a higher rate of diffusion. Determining an accurate glucose concentration in the subject may therefore depend on knowing the body temperature of the subject, which can affect the rate at which glucose diffuses from the subject into the sensing area.
- the body temperature sensor can be in the form of a patch that is worn on the skin. It can comprise an adhesive such as a hydro gel to attach to the subject's skin. It can also comprise one or more thermistors to sense the temperature of the patient's body. [0085]
- the temperature sensor can be either separate from the glucose monitor or incorporated into the glucose monitor.
- the body temperature sensor can be in wired communication with at least one other component, such as the electronics element so that the output from the body temperature sensor can be communicated to the, for example, electronics component where it can be used in the calculation of a glucose concentration or transmitted to a housing separate from the sensor where it can be then used in the calculation of a glucose concentration.
- the body temperature sensor may, however, be in communication with a different component or multiple components.
- the body temperature sensor can, however, include a transmitter for transmitting the sensed body temperature to the glucose monitor if, for example, the body temperature sensor is a patch worn separately from the glucose monitor housing or housings.
- the temperature sensor is incorporated into the glucose monitor and is located on the underside of the monitor, so that when the monitor is worn by the subject, the body temperature sensor is in contact with the skin.
- a separate body temperature adhesive may or may not be used, as the body temperature sensor may contact the skin simply by pressure from the glucose monitor.
- the glucose monitor includes a vibration assembly adapted to ease the penetration of the needle into the stratum corteum of the skin.
- the vibration assembly can include a vibration element such as a vibration motor which drives an unbalanced load or an off-set weight, as can be found in many commercial handheld devices such as cell phones or PDAs.
- the vibration element can be a different type of vibratory mechanism that can initiate a vibration effect to ease the penetration of the needle into the skin, such as an ultrasonic vibrator.
- the vibration element can cause the vibration of one or more components of the glucose monitor.
- the device Upon initiation of the vibration, the device can activate a separate force applicator that provides a force from the device towards the surface of the skin to assist in the needle penetration of the skin.
- the user can simply apply pressure with, for example, the palm side of the hand from on top of the glucose monitor towards the surface of the skin when the vibratory effect occurs to assist in the penetration of the skin.
- the vibration motor can be housed inside the glucose monitor in a configuration such that a torque results from the rotation of the motor (during the vibration) and the vibration motor causes a downward force from the glucose monitor towards the surface of the skin to assist the needle in penetrating the stratum corneum layer of the skin.
- the monitor can include an applicator to apply the sensor pad or adhesive pad to the skin.
- the applicator pad may be part of the sensor device or when the monitor includes separate components, it may be included in any of the different components.
- the needle(s) or tissue piercing element(s) 102, reservoirs 118 and 126, channel 108, sensor 112 and adhesive pads 116 are contained within a support structure (such as a housing 128) separate from electronics element 114 and actuator 120, which are supported within their own housing 130.
- a support structure such as a housing 1228 separate from electronics element 114 and actuator 120, which are supported within their own housing 130.
- This arrangement permits the sensor, sensing fluid and needle(s) to be discarded after a period of use (e.g., when reservoir 118 is depleted) while enabling the electronics and actuator to be reused.
- a flexible covering made, e.g., of polyester or other plastic-like material may surround and support the disposable components.
- FIG. 11 shows an exploded view of another embodiment of the invention. This figure shows a removable seal 203 covering the distal end of needle 202 and attached, e.g., by adhesive. Seal 203 retains the sensing fluid within the needle and sensing area prior to use and is removed prior to placing the glucose monitor 200 on the skin using adhesive pressure seal 216.
- needle 202, sensing fluid and waste reservoirs 218 and 226, sensing microchannel 208 and electrochemical glucose sensor 212 are contained within and/or supported by a housing 228 which forms the disposable portion of the device.
- a second housing 230 supports an electronics board or element 214 (containing, e.g., processing circuitry, a power source, transmission circuitry, etc.) and an actuator 220 that can be used to move sensing fluid out of reservoir 218, through microchannel 208 into waste reservoir 226.
- Electrical contacts 215 extend from electronics board 214 to make contact with corresponding electrodes in glucose sensor 212 when the device is assembled. While one needle is shown in Figure 11, more than one needle may be used, for example, as shown in Figures 5-6.
- the glucose monitor of Figure 11 may incorporate the deformed substrate layer defining a plurality of tissue piercing elements as described herein, and may replace substrate 206 and needle 202.
- Electrochemical sensors for glucose based on the specific glucose oxidizing enzyme glucose oxidase, have generated considerable interest.
- Several commercial devices based on this principle have been developed and are widely used currently for monitoring of glucose, e.g., self testing by patients at home, as well as testing in physician offices and hospitals.
- the earliest amperometric glucose biosensors were based on glucose oxidase (GOX) which generates hydrogen peroxide in the presence of oxygen and glucose according to the following reaction scheme: Glucose + GOX-FAD (ox) ⁇ » Gluconolactone + GOX-FADH 2 (red) GOX-FADH 2 (red) + O 2 ⁇ » GOX-FAD (ox) + H 2 O 2
- Electrochemical biosensors are used for glucose detection because of their high sensitivity, selectivity and low cost.
- amperometric detection is based on measuring either the oxidation or reduction of an electroactive compound at a working electrode (sensor).
- a constant potential is applied to that working electrode with respect to another electrode used as the reference electrode.
- the glucose oxidase enzyme is first reduced in the process but is reoxidized again to its active form by the presence of any oxygen resulting in the formation of hydrogen peroxide.
- Glucose sensors generally have been designed by monitoring either the hydrogen peroxide formation or the oxygen consumption.
- the hydrogen peroxide produced is easily detected at a potential of 0.0, 0.1, 0.2, or any other fixed potential relative to a reference electrode such as an Ag/ AgCl electrode.
- sensors based on hydrogen peroxide detection are subject to electrochemical interference by the presence of other oxidizable species in clinical samples such as blood or serum.
- biosensors that monitor oxygen consumption are affected by the variation of oxygen concentration in ambient air or in any of the fluids used with the monitors as described herein.
- different strategies have been developed and adopted.
- Selectively permeable membranes or polymer films have been used to suppress or minimize interference from endogenous electroactive species in biological samples.
- Another strategy to solve these problems is to replace oxygen with electrochemical mediators to reoxidize the enzyme.
- Mediators are electrochemically active compounds that can reoxidize the enzyme (glucose oxidase) and then be reoxidized at the working electrode as shown below:
- Conductive organic salts such as tetrathiafulvalene- tetracyanoquinodimethane (TTF-TCNQ) can operate as low as 0.0 Volts relative to a Ag/AgCl reference electrode.
- a working electrode 302 such as Pt, C, or Pt/C is referenced against a reference electrode 304 (such as Ag/AgCl) and a counter electrode 306, such as Pt, provides a means for current flow.
- the three electrodes are mounted on a substrate 308 then covered with a reagent 310, as shown in Figure 12(b).
- Figure 13 shows a two electrode system, wherein the working and auxiliary electrodes 402 and 404 are made of different electrically conducting materials.
- the electrodes 402 and 404 are mounted on a flexible substrate 408 as shown in Figure 13 and covered with a reagent 410, as shown in Figure 13(b).
- the working and auxiliary electrodes are made of the same electrically conducting materials, where the reagent exposed surface area of the auxiliary electrode is slightly larger than that of the working electrode or where both the working and auxiliary electrodes are substantially of equal dimensions.
- immobilization of the enzymes is also very important. Conventional methods of enzyme immobilization include covalent binding, physical adsorption or cross-linking to a suitable matrix may be used.
- the reagent is contained in a reagent well in the biosensor.
- the reagent includes a redox mediator, an enzyme, and a buffer, and covers substantially equal surface areas of portions of the working and auxiliary electrodes.
- a sample containing the analyte to be measured in this case glucose
- the analyte comes into contact with the glucose biosensor the analyte is oxidized, and simultaneously the mediator is reduced.
- an electrical potential difference is applied between the electrodes.
- the amount of oxidized form of the redox mediator at the auxiliary electrode and the applied potential difference must be sufficient to cause diffusion limited electrooxidation of the reduced form of the redox mediator at the surface of the working electrode.
- the current produced by the electrooxidation of the reduced form of the redox mediator is measured and correlated to the amount of the analyte concentration in the sample.
- the analyte sought to be measured may be reduced and the redox mediator may be oxidized.
- these requirements are satisfied by employing a readily reversible redox mediator and using a reagent with the oxidized form of the redox mediator in an amount sufficient to insure that the diffusion current produced is limited by the oxidation of the reduced form of the redox mediator at the working electrode surface.
- the amount of the oxidized form of the redox mediator at the surface of the auxiliary electrode must always exceed the amount of the reduced form of the redox mediator at the surface of the working electrode.
- the working and auxiliary electrodes may be substantially the same size or unequal size as well as made of the same or different electrically conducting material or different conducting materials. From a cost perspective the ability to utilize electrodes that are fabricated from substantially the same material represents an important advantage for inexpensive biosensors.
- the redox mediator must be readily reversible, and the oxidized form of the redox mediator must be of sufficient type to receive at least one electron from the reaction involving enzyme, analyte, and oxidized form of the redox mediator.
- enzymes and redox mediators that may be used in measuring particular analytes by the present invention are ferrocene and or ferrocene derivative, ferricyanide, and viologens. Buffers may be used to provide a preferred pH range from about 4 to 8.
- the most preferred pH range is from about 6 to 7.
- the most preferred buffer is phosphate (e.g., potassium phosphate) from about 0.01M to 0.5M and preferably about 0.05M. (These concentration ranges refer to the reagent composition before it is dried onto the electrode surfaces.) More details regarding glucose sensor chemistry and operation may be found in: Clark LC, and Lyons C, "Electrode Systems for Continuous Monitoring in Cardiovascular Surgery," Ann NY Acad Sci, 102:29, 1962; Updike SJ, and Hicks GP, "The Enzyme Electrode,” Nature, 214:986, 1967; Cass, A.E. G., G. Davis. G. D. Francis, et. al. 1984.
- FIG. 14 Another embodiment of the disposable portion of the glucose monitor invention is shown in Figure 14 with a needle 502 and a glucose sensor 512 in fluid communication with a sensing area in channel 508.
- actuator 520 is on the side of sensing fluid reservoir 518, and the waste reservoir 526 is expandable.
- actuator 520 sends sensing fluid from reservoir 518 through one way flap valve 522 into the sensing area in channel 508 and forces sensing fluid within channel 508 through flap valve 524 into the expandable waste reservoir 526. While one needle is shown more than one needle may be used. Alternatively, a deformed substrate layer as described herein may be used in the glucose monitor of Figure 14. [00104] In some of the embodiments described herein, the starting amount of sensing fluid in a sensing fluid reservoir is about 1.0 ml or less, and operation of the sensing fluid actuator sends about 5 ⁇ L to about 25 ⁇ L of fresh sensing fluid into the sensing channel. Recalibrating the device three times a day for seven days will use less than about 1000 ⁇ L of sensing fluid.
- FIGS 15 and 16 show a remote receiver for use with a glucose monitoring system.
- the wireless receiver can be configured to be worn by a patient on a belt, or carried in a pocket or purse.
- glucose sensor information is transmitted by the glucose sensor 602 applied to the user's skin to receiver 600 using, e.g., wireless communication such as radio frequency (RF) or Bluetooth wireless.
- RF radio frequency
- the receiver may maintain a continuous link with the sensor, or it may periodically receive information from the sensor.
- the sensor and its receiver may be synchronized using RFID technology or other unique identifiers.
- Receiver 600 may be provided with a display 604 and user controls 606.
- the display may show, e.g., glucose values, directional glucose trend arrows and rates of change of glucose concentration.
- the receiver can also be configured with a speaker adapted to deliver an audible alarm, such as high and low glucose alarms. Additionally, the receiver can include a memory device, such as a chip, that is capable of storing glucose data for analysis by the user or by a health care provider.
- a memory device such as a chip
- the monitor preferably the wireless receiver component
- the monitor can be programmed with high and low threshold levels such that when the patient's glucose levels are higher than the high threshold level or lower than the low threshold level the monitor will alert the patient or a third party.
- the receiver can be preprogrammed to default threshold levels, can be manually programmed using, for example, the receiver's user interface, or the receiver can be adapted to dynamically adjust threshold levels based on, for example, current glucose concentrations, trends in the glucose concentrations, or user inputs into the receiver such as an indication from the user that she is going to sleep or about to consume food.
- the alert can occur based on any method to alert the patient, such as, for example, with an audible alert like a beep, a visual alert such as a blinking light, or mechanical alert such as vibrating.
- the monitor can also be adapted to wirelessly alert a device separate from the receiver, such as a health care provider, when the glucose concentration is above or below the threshold levels, or trending below or above the threshold levels.
- the monitor, and preferably the receiver can also be adapted to display glucose concentration trends and can alert the patient' when the concentration is trending down or up. Trends can be stored in the receiver and can be used to dynamically adjust the threshold levels.
- the source reservoir for the calibration and sensing fluid may be in a blister pack which maintains its integrity until punctured or broken.
- the actuator may be a small syringe or pump. Use of the actuator for recalibration of the sensor may be performed manually by the user or may be performed automatically by the device if programmed accordingly.
- There may also be a spring or other loading mechanism within the reusable housing that can be activated to push the disposable portion — and specifically the microneedles — downward into the user's skin.
Abstract
The present invention includes methods and apparatus for continuous glucose monitoring of a patient. In one aspect a glucose monitor includes a plurality of substantially cylindrical tissue piercing elements adapted to pierce the stratum corneum and enter the epidermis, allowing for the diffusion of glucose from the interstitial fluid into the glucose monitors described herein. In another aspect of the invention, a glucose monitor includes a deformed substrate layer defining a plurality of tissue piercing elements.
Description
DEVICES, SYSTEMS, METHODS AND TOOLS FOR CONTINUOUS GLUCOSE MONITORING
CROSS-REFERENCE
[0001] This patent application is related to co-assigned pending Patent Applications Serial Number 11/277,731 filed March 28, 2006, and Serial Number 11/468,732 filed August 30, 2006, both of which are incorporated by reference herein in their entirety.
INCORPORATION BY REFERENCE
[0002] All publications and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference
BACKGROUND OF THE INVENTION
[0003] The invention relates to systems, devices, and tools, and the use of such systems, devices and tools for monitoring blood glucose levels in a person having diabetes. More specifically, the invention relates to systems, devices, and tools and the use of such systems, devices and tools for monitoring blood glucose level continuously, or substantially continuously.
[0004] Diabetes is a chronic, life-threatening disease for which there is no known cure. It is a syndrome characterized by hyperglycemia and relative insulin deficiency. Diabetes affects more than 120 million people world wide, and is projected to affect more than 220 million people by the year 2020. It is estimated that one out of every three children today will develop diabetes sometime during their lifetime. Diabetes is usually irreversible, and can lead to a variety of severe health complications, including coronary artery disease, peripheral vascular disease, blindness and stroke. The Center for Disease Control (CDC) has reported that there is a strong association between being overweight, obesity, diabetes, high blood pressure, high cholesterol, asthma and arthritis. Individuals with a body mass index of 40 or higher are more than 7 times more likely to be diagnosed with diabetes.
[0005] There are two main types of diabetes, Type I diabetes (insulin-dependent diabetes mellitus) and Type II diabetes (non-insulin-dependent diabetes mellitus). Varying
degrees of insulin secretory failure may be present in both forms of diabetes. In some instances, diabetes is also characterized by insulin resistance. Insulin is the key hormone used in the storage and release of energy from food.
[0006] As food is digested, carbohydrates are converted to glucose and glucose is absorbed into the blood stream primarily in the intestines. Excess glucose in the blood, e.g. following a meal, stimulates insulin secretion, which promotes entry of glucose into the cells, which controls the rate of metabolism of most carbohydrates. [0007] Insulin secretion functions to control the level of blood glucose both during fasting and after a meal, to keep the glucose levels at an optimum level. In a normal person blood glucose levels are between 80 and 90 mg/dL of blood during fasting and between 120 to 140 mg/dL during the first hour or so following a meal. For a person with diabetes, the insulin response does not function properly (either due to inadequate levels of insulin production or insulin resistance), resulting in blood glucose levels below 80 mg/dL during fasting and well above 140 mg/dL after a meal. [0008] Currently, persons suffering from diabetes have limited options for treatment, including taking insulin orally or by injection. In some instances, controlling weight and diet can impact the amount of insulin required, particularly for non-insulin dependent diabetics. Monitoring blood glucose levels is an important process that is used to help diabetics maintain blood glucose levels as near as normal as possible throughout the day. [0009] The blood glucose self-monitoring market is the largest self-test market for medical diagnostic products in the world, with a size of approximately over $3 billion in the United States and $7.0 billion worldwide. It is estimated that the worldwide blood glucose self-monitoring market will amount to $9.0 billion by 2008. Failure to manage the disease properly has dire consequences for diabetics. The direct and indirect costs of diabetes exceed $130 billion annually in the United States - about 20% of all healthcare costs.
[0010] There are two main types of blood glucose monitoring systems used by patients: single point or non-continuous and continuous. Non-continuous systems consist of meters and tests strips and require blood samples to be drawn from fingertips or alternate sites, such as forearms and legs (e.g. OneTouch® Ultra by LifeScan, Inc., Milpitas, CA, a Johnson & Johnson company). These systems rely on lancing and manipulation of the
fingers or alternate blood draw sites, which can be extremely painful and inconvenient, particularly for children.
[0011] Continuous monitoring sensors are generally implanted subcutaneously and measure glucose levels in the interstitial fluid at various periods throughout the day, providing data that shows trends in glucose measurements over a short period of time. These sensors are painful during insertion and usually require the assistance of a health care professional. Further, these sensors are intended for use during only a short duration (e.g., monitoring for a matter of days to determine a blood sugar pattern). Subcutaneously implanted sensors also frequently lead to infection and immune response complications. Another major drawback of currently available continuous monitoring devices is that they require frequent, often daily, calibration using blood glucose results that must be obtained from painful finger-sticks using traditional meters and test strips. This calibration, and re-calibration, is required to maintain sensor accuracy and sensitivity, but it can be cumbersome as well as painful.
[0012] At this time, there are four products approved by the FDA for continuous glucose monitoring, none of which are presently approved as substitutes for current glucose self- monitoring devices. Medtronic (www.medtronic.com) has two continuous glucose monitoring products approved for sale: Guardian® RT Real-Time Glucose Monitoring System and CGMS® System. Each product includes an implantable sensor that measures and stores glucose values for a period of up to three days. One product is a physician product. The sensor is required to be implanted by a physician, and the results of the data aggregated by the system can only be accessed by the physician, who must extract the sensor and download the results to a personal computer for viewing using customized software. The other product is a consumer product, which permits the user to download results to a personal computer using customized software. [0013] A third product approved for continuous glucose monitoring is the Glucowatch® developed by Cygnus Inc., which is worn on the wrist like a watch and can take glucose readings every ten to twenty minutes for up to twelve hours at a time. It requires a warm up time of 2 to 3 hours and replacement of the sensor pads every 12 hours. Temperature and perspiration are also known to affect its accuracy. The fourth approved product is a subcutaneously implantable glucose sensor developed by Dexcom, San Diego, CA
(www.dexcom.com). All of the approved devices are known to require daily, often frequent, calibrations with blood glucose values which the patient must obtain using conventional finger stick blood glucose monitors.
SUMMARY OF THE INVENTION
[0014] One aspect of the invention is a glucose monitor including at least one substantially cylindrical tissue piercing element having a distal opening, a proximal opening, and a substantially cylindrical interior lumen extending between the distal and proximal openings, a sensing area in fluid communication with the proximal opening of the at least one substantially cylindrical tissue piercing element, sensing fluid extending from the sensing area into substantially the entire interior lumen of the at least one substantially cylindrical tissue piercing element, and a glucose sensor adapted to sense a concentration of glucose in the sensing fluid within the sensing area. [0015] The monitor may also include a substrate coupled to and supporting the at least one substantially cylindrical tissue piercing element. The substrate can include a lumen in fluid communication with the proximal opening of the tissue piercing element and the sensing area.
[0016] In some embodiments the at least one tissue piercing element is made of a metal or alloy such as a stainless steel. The tissue piercing element may be tapered at its distal opening. The substantially cylindrical tissue piercing element is preferably configured to pierce only as deep as into the epidermis layer of the skin.
[0017] In some embodiments the monitor also includes a sensing fluid reservoir in fluid communication with the sensing area, wherein the sensing fluid reservoir is adapted to house a reservoir of sensing fluid with a known glucose concentration. The glucose monitor may also include an actuator such as a pump and/or valves configured to move fresh sensing fluid from the at least one sensing fluid reservoir into the sensing area. The actuator can be automatically or manually actuated. The monitor may also include a waste reservoir or waste unit in fluidic communication with the sensing area adapted to receive sensing fluid from the sensing area when the fresh sensing fluid is moved into the sensing area. In some embodiments the known glucose concentration is between about 0 mg/dl and about 400 mg/dl.
[0018] In some embodiments the sensing fluid reservoir is a first sensing fluid reservoir adapted to house a first sensing fluid with a first known glucose concentration, the glucose monitor further comprising a second sensing fluid reservoir adapted to house a second sensing fluid with a second known glucose concentration, wherein the first and second known glucose concentrations are not the same. In some embodiments the first known glucose concentration is between about 0 mg/dl and about 100 mg/dl and the second known glucose concentration is between about 100 mg/dl and about 400 mg/dl. [0019] In some embodiments the monitor includes a removable cover extending over the distal opening of the at least one substantially cylindrical tissue piercing element. [0020] In some embodiments the monitor includes a display adapted to display a glucose concentration. The sensor can be housed in a first housing and the display can be housed in a second housing, wherein the first housing comprises a transmitter to wirelessly transmit information indicative of the glucose concentration sensed by the sensor to a receiver in the second housing. The second housing can be adapted to determine the glucose concentration in the interstitial fluid and therefore the blood of the patient based on the information indicative of the glucose concentration sensed by the sensor. [0021] In some embodiments the monitor also includes an adhesive element adapted to attach the glucose monitor to the skin of a subject.
[0022] In some embodiments the glucose monitor is adapted to detect a concentration of glucose in the sensing fluid with the sensing area without extracting interstitial fluid through the distal opening into the interior lumen.
[0023] In some embodiments the monitor includes a temperature sensor adapted to sense the body temperature of the subject, and can also include a vibration assembly adapted to vibrate at least part of the glucose monitor to allow the at least one tissue piercing element to penetrate the stratum corneum.
[0024] Another aspect of the invention is a method of in vivo monitoring of an individual's interstitial fluid glucose concentration. The method comprises inserting distal ends of at least one substantially cylindrical tissue piercing element through a stratum corneum area of the individual's skin, the at least one tissue piercing element comprising a distal opening, a proximal opening, an interior lumen extending between
the distal and proximal openings, and a sensing fluid filling substantially the entire interior lumen, and sensing a glucose concentration of the sensing fluid.
[0025] In some embodiments a glucose sensor senses the glucose concentration, the method also includes calibrating the glucose sensor prior to the sensing step. The glucose sensor may be in fluid communication with a sensing area which is in fluid communication with the interior lumen. The sensing fluid can have a known glucose concentration, and calibrating the glucose sensor can include determining an output from the glucose sensor based on the known glucose concentration.
[0026] In some embodiments calibrating the glucose sensor also includes moving fresh sensing fluid with a known glucose concentration into the sensing area and determining an output from the glucose sensor based on the known glucose concentration of a fresh sensing fluid. The sensing fluid may be moved from the sensing area as the fresh sensing fluid is moved into the sensing area. Calibrating can include manually or automatically actuating an actuator which moves the fresh sensing fluid into the sensing area.
[0027] In some embodiments the method also include adhering the at least one tissue piercing element to the subject's skin with adhesive.
[0028] In some embodiments the method also includes permitting glucose to diffuse from interstitial fluid of the subject into the sensing area without extracting interstitial fluid through the distal opening in the interior lumen.
[0029] The method can also include sensing the subject's body temperature.
[0030] The method can further include determining a glucose concentration of the interstitial fluid of the subject wherein the determined glucose concentration is based on the sensed glucose concentration. The sensed glucose concentration can be transmitted to an external device separate from the device which houses the sensor, and the external device determines the glucose concentration of the interstitial fluid. The determined glucose concentration of the interstitial fluid can also be displayed.
[0031] Another aspect of the invention is a glucose monitor including a deformed substrate layer defining a plurality of tissue piercing elements each having a distal opening, a proximal opening and a lumen extending between the distal and proximal openings, a sensing area in fluid communication with the proximal openings of the
plurality of metal tissue piercing elements, sensing fluid extending from the sensing area into substantially the entire interior space of the plurality of tissue piercing elements, and a glucose sensor adapted to detect a concentration of glucose in the sensing fluid within the sensing area.
[0032] Other embodiments of the invention will be apparent from the specification and drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0033] The novel features of the invention are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present invention will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the invention are utilized, and the accompanying drawings of which:
[0034] Figures 1 and 2 are cross-sectional schematic views of a glucose monitoring device according to one embodiment of the invention with tissue piercing elements in place on a user's skin.
[0035] Figures 3-6 show exemplary substantially cylindrical needles of the present invention.
[0036] Figures 7 (a) - 7(c) show a method of forming deformed substrate layer of a glucose monitor.
[0037] Figure 8 shows a close up view of a distal opening of a tissue piercing element in a deformed substrate layer.
[0038] Figure 9 illustrates an exemplary deformed substrate layer defining a plurality of tissue piercing elements.
[0039] Figure 10 shows a perspective view of the optionally disposable portion of the glucose monitor.
[0040] Figure 11 shows an exploded view of a glucose monitoring device according to another embodiment of the invention.
[0041] Figures 12(a) and 12(b) are a schematic representative drawing of a three electrode system for use with the glucose sensor of one embodiment of this invention.
[0042] Figures 13(a) and 13(b) are a schematic representative drawing of a two electrode system for use with the glucose sensor of one embodiment of this invention.
[0043] Figure 14 is a cross-sectional schematic view of a portion of a glucose monitoring device according to yet another embodiment of the invention.
[0044] Figure 15 shows a remote receiver for use with a glucose monitoring system according to yet another embodiment of the invention.
[0045] Figure 16 shows a glucose sensor in place on a user's skin and a remote monitor for use with the sensor.
DETAILED DESCRIPTION OF THE INVENTION
[0046] The present invention provides a significant advance in biosensor and glucose monitoring technology: portable, painless, virtually non-invasive, self-calibrating, integrated and non-implanted sensors which continuously indicate the user's blood glucose concentration, enabling swift corrective action to be taken by the patient. The invention may also be used in critical care situations, such an in an intensive care unit to assist health care personnel. The sensor and monitor of this invention may be used to measure any other analyte as well, for example, electrolytes such as sodium or potassium ions. As will be appreciated by persons of skill in the art, the glucose sensor can be any suitable sensor including, for example, an electrochemical sensor or an optical sensor. [0047] Figure 1 shows a schematic cross-section of one embodiment of the glucose monitor. The glucose monitor 100 has one hollow needle 102 or other tissue piercing element extending through the stratum corneum 104 of a subject into the interstitial fluid 106 beneath the stratum corneum. The tissue piercing element is preferably hollow and has an open distal end, with an interior that communicates with a sensing area 110 within a sensor channel 108. Sensing area 110 is therefore in fluid communication with interstitial fluid 106 through needle 102. In this embodiment, sensing area 110 and the needle 102 are pre- filled with sensing fluid prior to the first use of the device. Thus, when the device is applied to the user's skin and the needle pierces the stratum corneum of the skin, there is substantially no net fluid transfer from the interstitial fluid into the needle. Rather, glucose diffuses from the interstitial fluid into the sensing fluid within the tissue piercing element as described below.
[0048] Figure 2 shows another embodiment of the glucose monitor with three (3) needles 102. The illustrated glucose monitors are not intended to be a limitation on the number of tissue piercing elements that can be used with a glucose monitor of the present
invention. The glucose monitor may have one, two, three, four, or more tissue piercing elements adapted to pierce the stratum corneum.
[0049] Figures 3 and 4 provide a side view and perspective view, respectively, of the needle shown in Figure 1. As shown, needle 2 engages and is coupled to a substrate or chip 6 of the glucose monitor. Needle 102 is substantially cylindrical in shape and has a substantially cylindrical interior lumen 4 shown in phantom which provides a channel between the distal opening 10 and the proximal opening of the needle 12. Substrate 6 has a substrate lumen 14 shown in phantom which is in fluid communication with the interior lumen of the needle 4 and the sensing area 8,
[0050] Figures 5 and 6 show an alternative embodiment wherein the glucose monitor has three (3) needles 2 to pierce the stratum corneum of the skin into the interstitial fluid.
As used herein, "needle" or "the needle" can refer to a single needle as shown in Figures
3 and 4, or more than one needle, as shown in Figures 5 and 6.
[0051] Figures 3-6 can also show needle or needles 2 passing through the interior of, and supported by, the substrate 6. The interior lumen of the needle would comprise lumen 4, lumen 14 and area 8 in Figures 3 and 5. In such embodiments the proximal opening of the needle is 15.
[0052] In this embodiment a passageway can be created in substrate 6 by any method known in the art, such as, for example, etching. A needle can then be inserted into the formed passageway to position the needle in the position shown in Figures 3-5, such as by press fitting. The needle can be a commercially available hypodermic needle and may or may not have to be altered before placing through and into substrate 6.
[0053] The tissue piercing elements are preferably made from any metal or alloy such as a stainless steel. Other metals of which the needle can be made are iron, brass, bronze, nickel, aluminum, chrome, titanium, platinum, gold, silver, tantalum, tungsten, iridium, palladium, rhodium, ruthenium, osmium, molybdenum, or cobalt. Commercially available hypodermic needles may be used in the glucose monitor, such as those manufactured by Becton Dickinson or UltiMed Incorporated.
[0054] Exemplary tissue piercing elements and their methods of production that can be used with the present invention can be found in U.S. Patent Number 7,076,987 to Martin et al. A commercially available hypodermic needle may need to be adapted before use
with the monitors as described herein. For example, for a desired tissue piercing element length of 1 mm, it may be necessary to shorten a commercially available hypodermic needle. Other processing steps such as, for example, laser cutting, grinding, or polishing the edges may be performed as well. If the tissue piercing element is not set at a right angle in relation to the monitor however, the length of the needle could be determined based on the degree of the angle.
[0055] In this embodiment the tissue piercing element is generally substantially cylindrical in shape, as shown in Figures 3-6. While the tissue piercing elements in Figures 3-6 are shown with circular cross-sections, they are not limited to such shapes. Substantially cylindrical tissue piercing elements includes tissue piercing elements that have cross-sections that are non-circular, such as hexagonal or any other cross-sectional shape.
[0056] The distal opening of the tissue piercing element can have a tapered cut as shown in Figures 3-6 to allow for quick and efficient penetration of the skin. The distal tapered end can have a variety of shape designs to allow for improved penetration, such as designs described in Patent No. 6,945,964, filed October 14, 2003. [0057] While the needles shown in Figures 3-6 are shown at a right angle to the substrate, the needle can be coupled to the substrate or pass through the substrate to assume any number of angles in relation to the substrate. For example, the needle can be at a 45 degree angle to the substrate such that the needle penetrates the skin at a 45 degree angle. In addition, the needles shown in Figures 3-6 are substantially straight. However, the needles may have a different shape such as a curved shape to allow for easier penetration in the skin. In embodiments in which multiple needles are used, the needles may have varying lengths to allow for easier penetration into the skin. [0058] A commercial hypodermic needle is generally available in a variety of gauges ranging from, for example, 7 to 35, but a hypodermic needle with a larger or smaller gauge number can be used. Generally, a small diameter is preferred to minimize the pain a patient will feel, however, a diameter that is too small may not provide enough structural support to penetrate the stratum corneum. In some embodiments the needle can be about 28 to about 32 gauge (i.e., about 0.36 millimeters outside diameter to about 0.23 millimeters outside diameter). In other embodiments the gauge can be about 35 or
smaller. Any other gauge/diameter needle may be used in the glucose monitor of the present invention.
[0059] The length of the tissue piercing element is preferably long enough to pierce the stratum corneum and come into contact with the interstitial fluid such that glucose from the interstitial fluid can diffuse through the needle as described below. Commercially available hypodermic needle can be coupled directly on the glucose monitor or through it, or can first be altered such as shortening the length to achieve a desirable length before engaging with the glucose monitor.
[0060] Suitable materials for the substrate include but are not limited to metals, alloys such as a stainless steel, plastic, silicon, germanium, minerals (e.g. quartz), semiconducting materials (e.g. silicon, germanium, etc.), ceramic, polymers and plastic. While the substrates as shown are in a generally rectangular shape, the substrate can be in any other shape or size as may be desirable to orient the substrate in the glucose monitor. In addition, a substrate lumen is shown in Figures 3-6 which can fluidly connect the interior lumen of the needle with the sensing area. The substrate lumen need not always be present and the interior lumen of the needle can be in direct fluid communication with the sensing area. The sensing area is shown in Figures 3-6, however the sensing area need not be located inside the substrate but can be in a separate channel above the substrate (not shown in Figures 3-6), shown as sensing area 208 in Figure 10 described below.
[0061] Fabrication of a lumen in the substrate and/or the sensing area in the substrate, such as lumen 14 and sensing area 10 in Figures 3-6 can be achieved by, for example, without limitation, a fabrication method including dry plasma etching, wet aqueous etching, water jet drilling, solid particles ablation and photon or electron beam drilling. [0062] The tissue piercing element can be a separate component from the substrate and can be attached to the substrate by an adhesive, glue, or other bonding technique such that the substrate lumen formed in the substrate aligns with the interior space of the needle to create a lumen extending from the distal opening of the needle to the sensing area through which the glucose can diffuse. While the substrate lumen 14 and interior lumen 4 are shown aligned in the same direction in Figures 3-6, the substrate lumen 14
could also form other passages for the glucose to diffuse. For example, substrate lumen 14 could form a number of right angles before connecting to the sensing area. [0063] Another aspect of the invention is a glucose monitor that comprises a deformed substrate layer defining a plurality of tissue piercing elements. Each of the tissue piercing elements has a distal opening, a proximal opening and a lumen or channel extending between the distal and proximal openings. The tissue piercing elements are preferably protrusions which are integrated with and extend from one side of the substrate. An exemplary method of manufacturing the tissue piercing elements will assist in describing their structure. Figures 7(a) - 7(c) are sectional views which show an exemplary method of producing the deformed substrate layer. Substrate actuator 70 comprises a plurality of pins or extensions 71 which extend from the base of substrate actuator 73. Substrate 72 is positioned below the substrate actuator 70. Substrate actuator 70 is lowered, in Figure 7(b), such that pins 71 engage and puncture substrate 72 creating distal openings 75. Substrate actuator 70 is then returned to its initial position in Figure 7(c), providing deformed substrate layer 77 defining tissue piercing elements 74.
[0064] Figure 9 illustrates an exemplary deformed substrate layer with an array of tissue piercing elements 74 with distal openings 75 and deformed substrate layer 77. [0065] By way of reference, the tissue piercing elements in this embodiment can be analogized to the rough protrusions of a cheese grater. Furthermore, the substrate actuator piercing through the substrate can be analogized to a pin puncturing a sheet of aluminum foil. Figures 7 and 8 illustrate one shape the tissue piercing elements can assume based on the shape and design of the pin used to puncture the substrate. In Figures 7 and 8 the tissue piercing elements have a general volcano shape, broader at their proximal end than at the distal end. The shape of the tissue piercing element will generally depend on the size and shape of the actuator pins.
[0066] In one embodiment the substrate actuator is a steel dye but can be any material capable of piercing through the substrate and create the distal openings. For example, the dye can have steel pins extending therefrom.
[0067] The substrate is preferably a metal sheet that can be made of any metal or alloy such as a stainless steel. Other exemplary metals that can be used alone or in
combination are iron, brass, bronze, nickel, aluminum, chrome, titanium, platinum, gold, silver, tantalum, tungsten, indium, palladium, rhodium, ruthenium, and osmium. The metal sheet is preferably of a thickness and strength such that the tissue piercing elements embedded therein are capable of piercing the stratum corneum of the skin to allow for glucose to diffuse through the distal opening of the tissue piercing elements. Similar to the tissue piercing elements described in Figures 3-6, the tissue piercing elements have interior lumens 76 (shown in Figure 8) which create a fluid network between the distal openings of the tissue piercing element and the sensing area. [0068] A deformed substrate layer can be configured to be disposed in the glucose monitor in the same or similar position as the tissue piercing elements in Figure 3-6. The deformed substrate layer could be in the same position as the substrate such that the distal opening would be in fluid communication with sensing area. [0069] Disposed above and in fluid communication with sensor channel 108 is a glucose sensor 112. In some embodiments, glucose sensor is an electrochemical glucose sensor that generates an electrical signal (current, voltage or charge) whose value depends on the concentration of glucose in the fluid within sensing area 110. Details of the operation of glucose sensor 112 are discussed below.
[0070] Sensor electronics element 114 is configured to receive an electrical signal from sensor 112. In some embodiments, sensor electronics element 114 uses the electrical signal to compute a glucose concentration and display it. In other embodiments, sensor electronics element 114 receives and transmits the electrical signal, or information derived from the electrical signal, to a remote device, such as through wireless communication. Electronics element 114 can comprise other circuitry such as an amplifier and an A/D converter which can amplify the electrical signal from the sensor and convert the amplified electrical signal to a digital signal before, for example, determining a glucose concentration or transmitting the digital signal to an external device which can then determine a glucose concentration. [0071] Glucose monitor 100 can be held in place on the skin 104 by one or more adhesive pads 116.
[0072] Glucose monitor 100 has a novel built-in sensor calibration system. A sensing fluid reservoir 118 contains a sensing fluid having, e.g., a known glucose concentration
between about 0 and about 400 mg/dl. In some embodiments, the glucose concentration in the sensing fluid is selected to be below the glucose sensing range of the sensor. The sensing fluid may also contain buffers, preservatives or other components in addition to the glucose. Upon manual or automatic actuation of a pump, plunger, or other actuator 120, fresh sensing fluid is forced from sensing fluid reservoir 118 through a check valve 122 (such as a flap valve) into sensing channel 108. Any sensing fluid within channel 108 is forced through a second check valve 124 (e.g., a flap valve) into a waste reservoir 126. Check valves or similar gating systems are used to prevent contamination. [0073] Because the fresh sensing fluid has a known glucose concentration, sensor 112 can be calibrated at this value to set a base line. After calibration, the sensing fluid in channel 108 remains stationary, and glucose from the interstitial fluid 106 diffuses through needle 102 into the sensing area 110. Changes in the glucose concentration over time reflect differences between the calibration glucose concentration of the sensing fluid in the sensing fluid reservoir 118 and the glucose concentration of the interstitial fluid, which can be correlated with the actual blood glucose concentration of the user using proprietary algorithms. Because of possible degradation of the sensor or loss of sensor sensitivity over time, the device may be periodically recalibrated by operating actuator 120 manually or automatically to send fresh sensing fluid from sensing fluid reservoir 118 into sensing area 110.
[0074] In some embodiments there may be two or more sensing fluid reservoirs as shown in Figure 10. A glucose monitor with two or more sensing fluid reservoirs can be calibrated at one or more different glucose concentrations, which can provide a more accurate calibration curve, which can therefore provide for a more accurate glucose concentration calculation.
[0075] Figure 10 shows a perspective view of the optionally disposable portion of the glucose monitor. Housing 60 includes a fluidic network in which a plurality of reservoirs and channels are in fluid communication to allow for the movement of sensing fluid (or calibration fluid) from at least one sensing fluid reservoir through a sensing area and into at least one waste reservoir. Housing 60 is coupled to seal 62 which is coupled to substrate or chip 64 which comprises at least one tissue piercing element 66.
[0076] As shown, housing 60 includes sensing fluid reservoirs 50 in fluid communication with sensing fluid channels 52, which are adapted to receive sensing fluid from the sensing fluid reservoirs. Sensing fluid channels 52 are in fluid communication with sensing area or sensing channel 54. Sensing area 54 is connected to waste channel 56, which is in fluid communication with waste reservoir 58. When substrate 64 is coupled to seal 62 and seal 62 is coupled to housing 60, the at least one tissue piercing element 66 is in fluid communication with sensing area 54. While not shown, a pump and/or series of valves can be incorporated into the glucose monitor to provide for the flow of fluid from the sensing fluid reservoirs to the waste reservoir. Also not shown is an actuator which can be manually or automatically actuated and work in tandem with a pump and/or series of valves to initiate the flow of fluid from the sensing fluid reservoirs. The channels shown in Figure 10 are intended to be optional in the glucose monitor, as the fluid can flow directly from the sensing fluid reservoirs into the sensing area, and further directly into the waste reservoirs. Similarly, one or more waste reservoirs may be incorporated into the glucose monitor. [0077] Waste reservoirs may be or include an absorption device such as a diaper-like material to absorb waste fluids. In such embodiments the waste reservoir may not necessarily be an enclosed structure, but may simply be an absorptive material in fluid communication with the sensing area so that it can absorb waste fluids as they are moved from the sensing area.
[0078] Incorporating a plurality of sensing fluid reservoirs into the glucose monitor, as shown in Figure 10, allows for a multiple point calibration curve to be generated during the glucose sensor calibration, which can provide a more accurate glucose concentration calculation. The sensing fluids in each of the different sensing fluid reservoirs can have different known glucose concentrations, enabling the glucose sensor to be calibrated at more than one calibration point, hi general, the more calibration points that can be used to generate a relationship between the concentration of sensed glucose in the sensing area and the glucose sensor output, the more accurate the results of the glucose concentration in the interstitial fluid, and therefore the blood, may be. In some embodiments a first sensing fluid has a glucose concentration of between about 0 mg/dl and about 100 mg/dl, and a second sensing fluid has a glucose concentration of between about 100 mg/dl and
about 400 mg/dl. When one or more sensing fluid reservoirs are used, the sensing fluids in each reservoir may, however, have substantially the same glucose concentration. [0079] While in some embodiments the glucose monitor may be manually actuated to initiate the calibrating procedure, the glucose monitor can also be self-calibrating or self- actuating. For example, the glucose monitor can include a programmable component, such as a timer, that is programmed to automatically activate a pump and valve system to initiate the flow of fresh sensing fluid from any of the sensing fluid reservoirs into the sensing area. The timer can be preprogrammed, or in some embodiments the monitor includes a first housing to be worn on the skin which includes the sensor and a second housing that is separate from the first housing that can display a glucose concentration. The second housing can be adapted such that it can program the programmable component in the first housing. For example, a patient may want to program the monitor to calibrate at certain times during the day. The first housing can include a timer that can be wirelessly programmed or reprogrammed by the patient using the second housing's user interface to start the calibration at certain times.
[0080] In one embodiment of monitoring a subject's interstitial fluid glucose concentration, the method includes calibrating the glucose sensor with a plurality of different sensing fluids, which may have different concentrations of glucose. A first sensing fluid of known glucose concentration can either be moved into the sensing area upon manufacture of the glucose monitor, or can be moved from a sensing fluid reservoir into the sensing area before the glucose monitor is first used. An output from the glucose sensor is detected by the electronics element and associated with the first known glucose concentration. Any actuating technique described herein may be used to move a second sensing fluid with a second known concentration from a second sensing fluid reservoir into the sensing area, forcing the first sensing fluid into the waste reservoir. The output from the glucose sensor can then be similarly detected by the electronics element and associated with the second known glucose concentration. Using these at least two associations of glucose concentration to glucose sensor output, a calibration curve or plot can be computed to relate glucose concentration to glucose sensor output, which can then be used to determine glucose concentration of the glucose that diffuses into the sensing area from the interstitial fluid. Any number of sensing fluids, and thus calibration points,
can be used to calibrate the glucose sensor. The calibrated sensor is then ready to sense a glucose concentration in the sensing area.
[0081] In embodiments where two or more sensing fluids with different glucose concentrations are used to calibrate the sensor, it may be advantageous to retain the fluid with the lower glucose concentration (such as a first concentration between about 0 mg/dl and 100 mg/dl) in the sensing area after the calibrating step, to provide for faster response times for the glucose sensing. In the method described above where the second sensing fluid has a higher glucose concentration, it may be advantageous to move a volume of fresh first sensing fluid into the sensing area after the glucose sensor output from the second sensing fluid is detected. This would move the second sensing fluid from the sensing area into waste reservoir.
[0082] In some embodiments at least one finger-stick calibration may optionally be performed or may be required to be performed at any point during the use of the monitors as described herein.
[0083] In some embodiments the glucose monitor includes a body temperature sensor. The body temperature sensor is adapted to detect the temperature of the body of the subject. As described herein, the glucose sensor senses a concentration of glucose in the sensing fluid within the sensing area. The concentration of glucose in the sensing fluid depends on the rate of diffusion of glucose molecules between the interstitial fluid in the subject and the sensing fluid in the sensing area. Diffusion is temperature dependent and as such the rate of the diffusion of glucose molecules between the interstitial fluid and the sensing fluid in the sensing area may depend on the body temperature of the subject. The rate of diffusion may increase as the body temperature increases, and may similarly decrease as the body temperature decreases. For example, a higher than normal body temperature can result in a higher rate of diffusion. Determining an accurate glucose concentration in the subject may therefore depend on knowing the body temperature of the subject, which can affect the rate at which glucose diffuses from the subject into the sensing area.
[0084] The body temperature sensor can be in the form of a patch that is worn on the skin. It can comprise an adhesive such as a hydro gel to attach to the subject's skin. It can also comprise one or more thermistors to sense the temperature of the patient's body.
[0085] The temperature sensor can be either separate from the glucose monitor or incorporated into the glucose monitor. The body temperature sensor can be in wired communication with at least one other component, such as the electronics element so that the output from the body temperature sensor can be communicated to the, for example, electronics component where it can be used in the calculation of a glucose concentration or transmitted to a housing separate from the sensor where it can be then used in the calculation of a glucose concentration. The body temperature sensor may, however, be in communication with a different component or multiple components. The body temperature sensor can, however, include a transmitter for transmitting the sensed body temperature to the glucose monitor if, for example, the body temperature sensor is a patch worn separately from the glucose monitor housing or housings. [0086] In one embodiment the temperature sensor is incorporated into the glucose monitor and is located on the underside of the monitor, so that when the monitor is worn by the subject, the body temperature sensor is in contact with the skin. In such embodiments, a separate body temperature adhesive may or may not be used, as the body temperature sensor may contact the skin simply by pressure from the glucose monitor. [0087] In some embodiments the glucose monitor includes a vibration assembly adapted to ease the penetration of the needle into the stratum corteum of the skin. The vibration assembly can include a vibration element such as a vibration motor which drives an unbalanced load or an off-set weight, as can be found in many commercial handheld devices such as cell phones or PDAs. The vibration element, however, can be a different type of vibratory mechanism that can initiate a vibration effect to ease the penetration of the needle into the skin, such as an ultrasonic vibrator. The vibration element can cause the vibration of one or more components of the glucose monitor. [0088] Upon initiation of the vibration, the device can activate a separate force applicator that provides a force from the device towards the surface of the skin to assist in the needle penetration of the skin. The user, however, can simply apply pressure with, for example, the palm side of the hand from on top of the glucose monitor towards the surface of the skin when the vibratory effect occurs to assist in the penetration of the skin. In some embodiments, however, when a vibration motor is used in the vibration assembly, the vibration motor can be housed inside the glucose monitor in a
configuration such that a torque results from the rotation of the motor (during the vibration) and the vibration motor causes a downward force from the glucose monitor towards the surface of the skin to assist the needle in penetrating the stratum corneum layer of the skin.
[0089] In some embodiments the monitor can include an applicator to apply the sensor pad or adhesive pad to the skin. The applicator pad may be part of the sensor device or when the monitor includes separate components, it may be included in any of the different components.
[0090] In some embodiments, the needle(s) or tissue piercing element(s) 102, reservoirs 118 and 126, channel 108, sensor 112 and adhesive pads 116 are contained within a support structure (such as a housing 128) separate from electronics element 114 and actuator 120, which are supported within their own housing 130. This arrangement permits the sensor, sensing fluid and needle(s) to be discarded after a period of use (e.g., when reservoir 118 is depleted) while enabling the electronics and actuator to be reused. A flexible covering (made, e.g., of polyester or other plastic-like material) may surround and support the disposable components. In particular, the interface between actuator 120 and reservoir 118 must permit actuator 120 to move sensing fluid out of reservoir 118, such as by deforming a wall of the reservoir. In these embodiments, housings 128 and 130 may have a mechanical connection, such as a snap or interference fit. [0091] Figure 11 shows an exploded view of another embodiment of the invention. This figure shows a removable seal 203 covering the distal end of needle 202 and attached, e.g., by adhesive. Seal 203 retains the sensing fluid within the needle and sensing area prior to use and is removed prior to placing the glucose monitor 200 on the skin using adhesive pressure seal 216. In this embodiment, needle 202, sensing fluid and waste reservoirs 218 and 226, sensing microchannel 208 and electrochemical glucose sensor 212 are contained within and/or supported by a housing 228 which forms the disposable portion of the device. A second housing 230 supports an electronics board or element 214 (containing, e.g., processing circuitry, a power source, transmission circuitry, etc.) and an actuator 220 that can be used to move sensing fluid out of reservoir 218, through microchannel 208 into waste reservoir 226. Electrical contacts 215 extend from electronics board 214 to make contact with corresponding electrodes in glucose
sensor 212 when the device is assembled. While one needle is shown in Figure 11, more than one needle may be used, for example, as shown in Figures 5-6. In addition, the glucose monitor of Figure 11 may incorporate the deformed substrate layer defining a plurality of tissue piercing elements as described herein, and may replace substrate 206 and needle 202.
[0092] The following is a description of glucose sensors that may be used with the glucose monitors of this invention. In 1962 Clark and Lyons proposed the first enzyme electrode (that was implemented later by Updike and Hicks) to determine glucose concentration in a sample by combining the specificity of a biological system with the simplicity and sensitivity of an electrochemical transducer. The most common strategies for glucose detection are based on using either glucose oxidase or glucose dehydrogenase enzyme.
[0093] Electrochemical sensors for glucose, based on the specific glucose oxidizing enzyme glucose oxidase, have generated considerable interest. Several commercial devices based on this principle have been developed and are widely used currently for monitoring of glucose, e.g., self testing by patients at home, as well as testing in physician offices and hospitals. The earliest amperometric glucose biosensors were based on glucose oxidase (GOX) which generates hydrogen peroxide in the presence of oxygen and glucose according to the following reaction scheme: Glucose + GOX-FAD (ox) ■» Gluconolactone + GOX-FADH2 (red) GOX-FADH2 (red) + O2 ■» GOX-FAD (ox) + H2O2
[0094] Electrochemical biosensors are used for glucose detection because of their high sensitivity, selectivity and low cost. In principal, amperometric detection is based on measuring either the oxidation or reduction of an electroactive compound at a working electrode (sensor). A constant potential is applied to that working electrode with respect to another electrode used as the reference electrode. The glucose oxidase enzyme is first reduced in the process but is reoxidized again to its active form by the presence of any oxygen resulting in the formation of hydrogen peroxide. Glucose sensors generally have been designed by monitoring either the hydrogen peroxide formation or the oxygen consumption. The hydrogen peroxide produced is easily detected at a potential of 0.0, 0.1, 0.2, or any other fixed potential relative to a reference electrode such as an Ag/ AgCl
electrode. However, sensors based on hydrogen peroxide detection are subject to electrochemical interference by the presence of other oxidizable species in clinical samples such as blood or serum. On the other hand, biosensors that monitor oxygen consumption are affected by the variation of oxygen concentration in ambient air or in any of the fluids used with the monitors as described herein. In order to overcome these drawbacks, different strategies have been developed and adopted. [0095] Selectively permeable membranes or polymer films have been used to suppress or minimize interference from endogenous electroactive species in biological samples. Another strategy to solve these problems is to replace oxygen with electrochemical mediators to reoxidize the enzyme. Mediators are electrochemically active compounds that can reoxidize the enzyme (glucose oxidase) and then be reoxidized at the working electrode as shown below:
GOX-FADH2 (red) + Mediator (ox) -> GOX-FAD (ox) + Mediator (red) [0096] Organic conducting salts, ferrocene and ferrocene derivatives, ferricyanide, quinones, and viologens are considered good examples of such mediators. Such electrochemical mediators act as redox couples to shuttle electrons between the enzyme and electrode surface. Because mediators can be detected at lower oxidation potentials than that used for the detection of hydrogen peroxide the interference from electroactive species (e.g., ascorbic and uric acids present) in clinical samples such as blood or serum is greatly reduced. For example ferrocene derivatives have oxidation potentials in the +0.1 to 0.4 V range. Conductive organic salts such as tetrathiafulvalene- tetracyanoquinodimethane (TTF-TCNQ) can operate as low as 0.0 Volts relative to a Ag/AgCl reference electrode. Nankai et al, WO 86/07632, published Dec. 31, 1986, discloses an amperometric biosensor system in which a fluid containing glucose is contacted with glucose oxidase and potassium ferricyanide. The glucose is oxidized and the ferricyanide is reduced to ferrocyanide. This reaction is catalyzed by glucose oxidase. After two minutes, an electrical potential is applied, and a current caused by the re- oxidation of the ferrocyanide to ferricyanide is obtained. The current value, obtained a few seconds after the potential is applied, correlates to the concentration of glucose in the fluid.
[0097] There are multiple glucose sensors that may be used with this invention. In a three electrode system, shown in Figure 12 a working electrode 302, such as Pt, C, or Pt/C is referenced against a reference electrode 304 (such as Ag/AgCl) and a counter electrode 306, such as Pt, provides a means for current flow. The three electrodes are mounted on a substrate 308 then covered with a reagent 310, as shown in Figure 12(b). [0098] Figure 13 shows a two electrode system, wherein the working and auxiliary electrodes 402 and 404 are made of different electrically conducting materials. Like the embodiment of Figure 12, the electrodes 402 and 404 are mounted on a flexible substrate 408 as shown in Figure 13 and covered with a reagent 410, as shown in Figure 13(b). In an alternative two electrode system, the working and auxiliary electrodes are made of the same electrically conducting materials, where the reagent exposed surface area of the auxiliary electrode is slightly larger than that of the working electrode or where both the working and auxiliary electrodes are substantially of equal dimensions. [0099] In amperometric and coulometric biosensors, immobilization of the enzymes is also very important. Conventional methods of enzyme immobilization include covalent binding, physical adsorption or cross-linking to a suitable matrix may be used. [00100] In some embodiments, the reagent is contained in a reagent well in the biosensor. The reagent includes a redox mediator, an enzyme, and a buffer, and covers substantially equal surface areas of portions of the working and auxiliary electrodes. When a sample containing the analyte to be measured, in this case glucose, comes into contact with the glucose biosensor the analyte is oxidized, and simultaneously the mediator is reduced. After the reaction is complete, an electrical potential difference is applied between the electrodes. In general the amount of oxidized form of the redox mediator at the auxiliary electrode and the applied potential difference must be sufficient to cause diffusion limited electrooxidation of the reduced form of the redox mediator at the surface of the working electrode. After a short time delay, the current produced by the electrooxidation of the reduced form of the redox mediator is measured and correlated to the amount of the analyte concentration in the sample. In some cases, the analyte sought to be measured may be reduced and the redox mediator may be oxidized. [00101] In the present invention, these requirements are satisfied by employing a readily reversible redox mediator and using a reagent with the oxidized form of the redox
mediator in an amount sufficient to insure that the diffusion current produced is limited by the oxidation of the reduced form of the redox mediator at the working electrode surface. For current produced during electrooxidation to be limited by the oxidation of the reduced form of the redox mediator at the working electrode surface, the amount of the oxidized form of the redox mediator at the surface of the auxiliary electrode must always exceed the amount of the reduced form of the redox mediator at the surface of the working electrode. Importantly, when the reagent includes an excess of the oxidized form of the redox mediator, as described below, the working and auxiliary electrodes may be substantially the same size or unequal size as well as made of the same or different electrically conducting material or different conducting materials. From a cost perspective the ability to utilize electrodes that are fabricated from substantially the same material represents an important advantage for inexpensive biosensors. [00102] As explained above, the redox mediator must be readily reversible, and the oxidized form of the redox mediator must be of sufficient type to receive at least one electron from the reaction involving enzyme, analyte, and oxidized form of the redox mediator. For example, when glucose is the analyte to be measured and glucose oxidase is the enzyme, ferricyanide or quinone may be the oxidized form of the redox mediator. Other examples of enzymes and redox mediators (oxidized form) that may be used in measuring particular analytes by the present invention are ferrocene and or ferrocene derivative, ferricyanide, and viologens. Buffers may be used to provide a preferred pH range from about 4 to 8. The most preferred pH range is from about 6 to 7. The most preferred buffer is phosphate (e.g., potassium phosphate) from about 0.01M to 0.5M and preferably about 0.05M. (These concentration ranges refer to the reagent composition before it is dried onto the electrode surfaces.) More details regarding glucose sensor chemistry and operation may be found in: Clark LC, and Lyons C, "Electrode Systems for Continuous Monitoring in Cardiovascular Surgery," Ann NY Acad Sci, 102:29, 1962; Updike SJ, and Hicks GP, "The Enzyme Electrode," Nature, 214:986, 1967; Cass, A.E. G., G. Davis. G. D. Francis, et. al. 1984. Ferrocene -mediated enzyme electrode for amperometric determination of glucose. Anal.Chem. 56:667-671; and Boutelle, M.G.,C. Stanford. M. Fillenz, et al. 1986. An amperometric enzyme electrode for monitoring brain glucose in the freely moving rat. Neurosci lett. 72:283-288.
[00103] Another embodiment of the disposable portion of the glucose monitor invention is shown in Figure 14 with a needle 502 and a glucose sensor 512 in fluid communication with a sensing area in channel 508. In this embodiment, actuator 520 is on the side of sensing fluid reservoir 518, and the waste reservoir 526 is expandable. Operation of actuator 520 sends sensing fluid from reservoir 518 through one way flap valve 522 into the sensing area in channel 508 and forces sensing fluid within channel 508 through flap valve 524 into the expandable waste reservoir 526. While one needle is shown more than one needle may be used. Alternatively, a deformed substrate layer as described herein may be used in the glucose monitor of Figure 14. [00104] In some of the embodiments described herein, the starting amount of sensing fluid in a sensing fluid reservoir is about 1.0 ml or less, and operation of the sensing fluid actuator sends about 5 μL to about 25 μL of fresh sensing fluid into the sensing channel. Recalibrating the device three times a day for seven days will use less than about 1000 μL of sensing fluid.
[00105] Figures 15 and 16 show a remote receiver for use with a glucose monitoring system. The wireless receiver can be configured to be worn by a patient on a belt, or carried in a pocket or purse. In this embodiment, glucose sensor information is transmitted by the glucose sensor 602 applied to the user's skin to receiver 600 using, e.g., wireless communication such as radio frequency (RF) or Bluetooth wireless. The receiver may maintain a continuous link with the sensor, or it may periodically receive information from the sensor. The sensor and its receiver may be synchronized using RFID technology or other unique identifiers. Receiver 600 may be provided with a display 604 and user controls 606. The display may show, e.g., glucose values, directional glucose trend arrows and rates of change of glucose concentration. The receiver can also be configured with a speaker adapted to deliver an audible alarm, such as high and low glucose alarms. Additionally, the receiver can include a memory device, such as a chip, that is capable of storing glucose data for analysis by the user or by a health care provider.
[00106] The monitor, preferably the wireless receiver component, can be programmed with high and low threshold levels such that when the patient's glucose levels are higher than the high threshold level or lower than the low threshold level the
monitor will alert the patient or a third party. The receiver can be preprogrammed to default threshold levels, can be manually programmed using, for example, the receiver's user interface, or the receiver can be adapted to dynamically adjust threshold levels based on, for example, current glucose concentrations, trends in the glucose concentrations, or user inputs into the receiver such as an indication from the user that she is going to sleep or about to consume food. The alert can occur based on any method to alert the patient, such as, for example, with an audible alert like a beep, a visual alert such as a blinking light, or mechanical alert such as vibrating. The monitor can also be adapted to wirelessly alert a device separate from the receiver, such as a health care provider, when the glucose concentration is above or below the threshold levels, or trending below or above the threshold levels. The monitor, and preferably the receiver, can also be adapted to display glucose concentration trends and can alert the patient' when the concentration is trending down or up. Trends can be stored in the receiver and can be used to dynamically adjust the threshold levels.
[00107] In some embodiments, the source reservoir for the calibration and sensing fluid may be in a blister pack which maintains its integrity until punctured or broken. The actuator may be a small syringe or pump. Use of the actuator for recalibration of the sensor may be performed manually by the user or may be performed automatically by the device if programmed accordingly. There may also be a spring or other loading mechanism within the reusable housing that can be activated to push the disposable portion — and specifically the microneedles — downward into the user's skin. [00108] While preferred embodiments of the present invention have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the invention. It should be understood that various alternatives to the embodiments of the invention described herein may be employed in practicing the invention. It is intended that the following claims define the scope of the invention and that methods and structures within the scope of these claims and their equivalents be covered thereby.
Claims
1. A glucose monitor, comprising: at least one substantially cylindrical tissue piercing element having a distal opening, a proximal opening, and an interior lumen extending between the distal and proximal openings; a sensing area in fluid communication with the proximal opening of the at least one substantially cylindrical tissue piercing element; sensing fluid extending from the sensing area into substantially the entire interior lumen of the at least one substantially cylindrical tissue piercing element; and a glucose sensor adapted to detect glucose in the sensing fluid within the sensing area.
2. The glucose monitor of claim 1 further comprising a substrate coupled to and supporting the at least one substantially cylindrical tissue piercing element.
3. The glucose monitor of claim 2 wherein the substrate comprises a lumen in fluid communication with the proximal opening of the tissue piercing element and the sensing area.
4. The glucose monitor of claim 1 wherein the at least one tissue piercing element is made of a metal or alloy.
5. The glucose monitor of claim 4 wherein the metal or alloy is a stainless steel.
6. The glucose monitor of clam 1 wherein the at least one substantially cylindrical tissue piercing element is tapered near its distal opening.
7. The glucose monitor of claim 1 wherein the at least one substantially cylindrical tissue piercing element is configured to pierce only as deep as into the epidermis.
8. The glucose monitor of claim 1 further comprising a sensing fluid reservoir in fluid communication with the sensing area, wherein the sensing fluid reservoir is adapted to house a reservoir of sensing fluid with a known glucose concentration.
9. The glucose monitor of claim 8 further comprising an actuator configured to move fresh sensing fluid from the at least one sensing fluid reservoir into the sensing area.
10. The glucose monitor of claim 9 further comprising a waste reservoir in fluidic communication with the sensing area adapted to receive sensing fluid from the sensing area when the fresh sensing fluid is moved into the sensing area.
11. The glucose monitor of claim 9 wherein the actuator comprises a pump and/or a valve.
12. The glucose monitor of claim 9 wherein the actuator is configured to be manually actuated.
13. The glucose monitor of claim 9 wherein the actuator is configured to be automatically actuated.
14. The glucose monitor of claim 13 wherein the monitor further comprises a programmable component in communication with the actuator wherein the programmable component is programmed to automatically actuate the actuator.
15. The glucose monitor of claim 14 wherein the programmable component is configured to be programmed using a device that is not housed with the sensor.
14. The glucose monitor of claim 8 wherein the known glucose concentration is between about 0 mg/dl and about 400 mg/dl.
16. The glucose monitor of claim 8 wherein the sensing fluid reservoir is a first sensing fluid reservoir adapted to house a first sensing fluid with a first known glucose concentration, the glucose monitor further comprising a second sensing fluid reservoir adapted to house a second sensing fluid with a second known glucose concentration, wherein the first and second known glucose concentrations are not the same.
17. The glucose monitor of claim 16 wherein the first known glucose concentration is between about 0 mg/dl and about 100 mg/dl and the second known glucose concentration is between about 100 mg/dl and about 400 mg/dl.
18. The glucose monitor of claim 8 further comprising a housing comprising a first part and a second part, the first part of the housing being adapted to support the at least one substantially cylindrical tissue piercing elements, the sensing fluid reservoir, the sensing area, and at least part of the glucose sensor, the second part of the housing comprising an electrical connection to the at least part of the glucose sensor in the first part of the housing, the housing further comprising a connector adapted to connect and disconnect the first part of the housing from the second part of the housing.
19. The glucose monitor of claim 1 further comprising a removable cover extending over the distal opening of the at least one substantially cylindrical tissue piercing element.
20. The glucose monitor of claim 1 further comprising a display adapted to display a glucose concentration sensed by the sensor.
21. The glucose monitor of claim 20 wherein the sensor is housed in a first housing and the display is housed in a second housing separate from the first housing, wherein
the first housing comprises a transmitter to wirelessly transmit information indicative of the glucose concentration sensed by the sensor to a receiver in the second housing.
22. The glucose monitor of claim 21 wherein the second housing is adapted to determine the glucose concentration in the blood of the subject based on the information indicative of the glucose concentration sensed by the sensor.
23. The glucose monitor of claim 1 further comprising an adhesive element adapted to attach the glucose monitor to the skin of a subject.
24. The glucose monitor of claim 1 wherein the glucose monitor is further adapted to detect a concentration of glucose in the sensing fluid with the sensing area without extracting interstitial fluid through the distal opening into the interior lumen.
25. The glucose monitor of claim 1 further comprising a body temperature sensor adapted to sense the body temperature of the subject.
26. The glucose monitor of claim 1 further comprising a vibration assembly adapted to vibrate at least part of the glucose monitor such that the at least one tissue piercing element penetrates the stratum corneum.
27. A method of in vivo monitoring of an individual's interstitial fluid glucose concentration comprising: inserting a distal end of at least one substantially cylindrical tissue piercing element through a stratum corneum area of the individual's skin, the at least one tissue piercing element comprising a distal opening, a proximal opening, an interior lumen extending between the distal and proximal openings, and a sensing fluid filling substantially the entire interior lumen; and sensing a glucose concentration of the sensing fluid.
28. The method of claim 27 wherein a glucose sensor senses the glucose concentration, the method further comprising calibrating the glucose sensor prior to the sensing step.
29. The method of claim 28 wherein the glucose sensor is in fluid communication with a sensing area which is in fluid communication with the interior lumen of the at least one tissue piercing element.
30. The method of claim 28 wherein the sensing fluid has a known glucose concentration, and calibrating the glucose sensor comprises determining an output from the glucose sensor based on the known glucose concentration.
31. The method of claim 30 wherein calibrating the glucose sensor further comprises moving fresh sensing fluid with the known glucose concentration into the sensing area and determining the output from the glucose sensor based on the known glucose concentration of the fresh sensing fluid.
32. The method of claim 31 wherein the calibrating further comprises moving the sensing fluid from the sensing area as the fresh sensing fluid is moved into the sensing area.
33. The method of claim 31 wherein calibrating comprises actuating an actuator which moves the fresh sensing fluid into the sensing area.
34. The method of claim 33 wherein actuating comprises manually actuating the actuator.
35. The method of claim 33 wherein actuating comprises automatically actuating the actuator.
36. The method of claim 35 wherein the actuator is adapted to be programmed to be automatically actuated.
37. The method of claim 27 further comprising adhering the monitor to the subject's skin with adhesive.
38. The method of claim 29 further comprising permitting glucose to diffuse from interstitial fluid of the subject into the sensing area without extracting interstitial fluid through the distal opening in the interior lumen.
39. The method of claim 27 further comprising sensing the subject's body temperature.
40. The method of claim 27 further comprising determining a glucose concentration of the interstitial fluid of the subject wherein the determined glucose concentration is based on the sensed glucose concentration.
41. The method of claim 40 wherein an output from the sensor indicative of the sensed concentration is transmitted to an external device separate from the sensor, and the external device determines the glucose concentration of the interstitial fluid based on the output from the sensor.
42. The method of claim 41 further comprising displaying the determined glucose concentration of the interstitial fluid.
43. The method of claim 41 wherein the external device determines the concentration of glucose in the patient's blood based on the glucose concentration of the interstitial fluid.
44. A glucose monitor, comprising:
a deformed substrate layer defining a plurality of tissue piercing elements each having a distal opening, a proximal opening and a lumen extending between the distal and proximal openings; a sensing area in fluid communication with the proximal openings of the plurality of metal tissue piercing elements; sensing fluid extending from the sensing area into substantially the entire interior space of the plurality of tissue piercing elements; and a glucose sensor adapted to detect glucose in the sensing fluid within the sensing area.
45. The monitor of claim 44 wherein the deformed substrate layer is made of metal or an alloy.
46. The monitor of claim 45 wherein the deformed substrate layer is an alloy and is a stainless steel.
47. The monitor of claim 44 wherein the deformed substrate layer has been deformed by an external actuator.
48. The monitor of claim 47 wherein the external actuator comprises a plate having a plurality of pins extending therefrom, wherein the pins are adapted to pass through the substrate layer thereby deforming the substrate layer and creating the tissue piercing elements, the distal and proximal openings, and the lumens.
49. The monitor of claim 44 wherein the plurality of tissue piercing elements have a substantial volcano shape.
50. The monitor of claim 44 wherein at least one of the plurality of tissue piercing elements has a distal opening with a smaller radius than the radius of the proximal opening.
51. The monitor of claim 44 wherein the distal end of the plurality of tissue piercing elements comprise a plurality of protrusions.
52. The monitor of claim 44 wherein the plurality of tissue piercing element are configured to pierce only as deep as into the epidermis.
53. The monitor of claim 44 further comprising a sensing fluid reservoir in fluid communication with the sensing area, wherein the sensing fluid reservoir is adapted to house a reservoir of sensing fluid with a known glucose concentration.
54. The monitor of claim 53 further comprising an actuator configured to move fresh sensing fluid from the at least one sensing fluid reservoir into the sensing area.
55. The monitor of claim 54 further comprising a waste reservoir in fluidic communication with the sensing area adapted to receive sensing fluid from the sensing area when the fresh sensing fluid is moved into the sensing area.
56. The monitor of claim 54 wherein the actuator comprises a pump and/or a valve.
57. The monitor of claim 54 wherein the actuator is configured to be manually actuated.
58. The monitor of claim 54 wherein the actuator is configured to be automatically actuated.
59. The monitor of claim 53 wherein the known glucose concentration is between about 0 mg/dl and about 400 mg/dl.
60. The monitor of claim 53 wherein the sensing fluid reservoir is a first sensing fluid reservoir adapted to house a first sensing fluid with a first known glucose concentration, the glucose monitor further comprising a second sensing fluid reservoir adapted to house
a second sensing fluid with a second known glucose concentration, wherein the first and second known glucose concentrations are not the same.
61. The monitor of claim 60 wherein the first known glucose concentration is between about 0 mg/dl and about 100 mg/dl and the second known glucose concentration is between about 100 mg/dl and about 400 mg/dl.
62. The glucose monitor of claim 54 further comprising a housing comprising a first part and a second part, the first part of the housing being adapted to support the at least one substantially cylindrical tissue piercing elements, the sensing fluid reservoir, the sensing area, and at least part of the glucose sensor, the second part of the housing comprising an electrical connection to the at least part of the glucose sensor in the first part of the housing, the housing further comprising a connector adapted to connect and disconnect the first part of the housing from the second part of the housing.
63. The monitor of claim 44 further comprising a removable cover extending over the distal opening of the at least one substantially cylindrical tissue piercing element.
64. The monitor of claim 44 further comprising a display adapted to display a glucose concentration sensed by the sensor.
65. The monitor of claim 64 wherein the sensor is housed in a first housing and the display is housed in a second housing, wherein the first housing comprises a transmitter to wirelessly transmit information indicative of the glucose concentration sensed by the sensor to a receiver housed in the second housing.
66. The monitor of claim 65 wherein the second housing is adapted to determine the glucose concentration in the blood of the subject based on the information indicative of the glucose concentration sensed by the sensor.
67. The monitor of claim 44 further comprising an adhesive element adapted to attach the glucose monitor to the skin of a subject.
68. The monitor of claim 44 wherein the glucose monitor is further adapted to detect a concentration of glucose in the sensing fluid with the sensing area without extracting interstitial fluid through the distal opening into the interior lumen.
69. The monitor of claim 44 further comprising a body temperature sensor adapted to sense the body temperature of the subject.
70. The monitor of claim 44 further comprising a vibration assembly adapted to vibrate at least part of the glucose monitor to allow the at least one tissue piercing element to penetrate the stratum corneum.
71. A method of in vivo monitoring of a patient' s interstitial fluid glucose concentration comprising: inserting distal ends of a plurality of tissue piercing elements defined by a deformed substrate layer through a stratum corneum area of a patient's skin, the at least one tissue piercing element comprising a distal opening, a proximal opening, an interior lumen extending between the distal and proximal openings, and a sensing fluid filling substantially the entire interior lumen; and sensing a glucose concentration of the sensing fluid.
72. The method of claim 71 wherein a glucose sensor senses the glucose concentration, the method further comprising calibrating the glucose sensor prior to the sensing step.
73. The method of claim 72 wherein the glucose sensor is in fluid communication with a sensing area which is in fluid communication with the interior lumen of the plurality of tissue piercing elements.
74. The method of claim 72 wherein the sensing fluid has a known glucose concentration, and calibrating the glucose sensor comprises determining an output from the glucose sensor based on the known glucose concentration.
75. The method of claim 74 wherein calibrating the glucose sensor further comprises moving fresh sensing fluid with the known glucose concentration into the sensing area and determining the output from the glucose sensor based on the known glucose concentration of the fresh sensing fluid.
76. The method of claim 75 wherein the calibrating further comprises moving the sensing fluid from the sensing area as the fresh sensing fluid is moved into the sensing area.
77. The method of claim 75 wherein calibrating comprises actuating an actuator which moves the fresh sensing fluid into the sensing area.
78. The method of claim 77 wherein actuating comprises manually actuating the actuator.
79. The method of claim 77 wherein actuating comprises automatically actuating the actuator.
80. The method of claim 79 wherein the actuator is adapted to be programmed to be automatically actuated.
81. The method of claim 71 further comprising adhering the monitor to the subject's skin with adhesive.
82. The method of claim 73 further comprising permitting glucose to diffuse from interstitial fluid of the patient into the sensing area without extracting interstitial fluid through the distal opening in the interior lumen.
83. The method of claim 71 further comprising sensing the subject's body temperature.
84. The method of claim 71 further comprising determining a glucose concentration of the interstitial fluid of the subject wherein the determined glucose concentration is based on the sensed glucose concentration.
85. The method of claim 84 wherein an output from the sensor indicative of the sensed concentration is transmitted to an external device separate from the sensor, and the external device determines the glucose concentration of the interstitial fluid based on the output from the sensor.
86. The method of claim 85 further comprising displaying the determined glucose concentration of the interstitial fluid.
87. The method of claim 85 wherein the external device determines the concentration of glucose in the patient's blood based on the glucose concentration of the interstitial fluid.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07865939A EP2122309A2 (en) | 2006-12-20 | 2007-12-20 | Devices, systems, methods and tools for continuous glucose monitoring |
CA002670020A CA2670020A1 (en) | 2006-12-20 | 2007-12-20 | Devices, systems, methods and tools for continuous glucose monitoring |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/642,196 | 2006-12-20 | ||
US11/642,196 US20080154107A1 (en) | 2006-12-20 | 2006-12-20 | Device, systems, methods and tools for continuous glucose monitoring |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008077147A2 true WO2008077147A2 (en) | 2008-06-26 |
WO2008077147A3 WO2008077147A3 (en) | 2008-10-16 |
Family
ID=39537084
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2007/088456 WO2008077147A2 (en) | 2006-12-20 | 2007-12-20 | Devices, systems, methods and tools for continuous glucose monitoring |
Country Status (4)
Country | Link |
---|---|
US (1) | US20080154107A1 (en) |
EP (1) | EP2122309A2 (en) |
CA (1) | CA2670020A1 (en) |
WO (1) | WO2008077147A2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009049243A2 (en) * | 2007-10-12 | 2009-04-16 | Arkal Medical, Inc. | Microneedle array with diverse needle configurations |
CN106236108A (en) * | 2016-08-30 | 2016-12-21 | 张胜国 | Intelligence Wicresoft blood glucose continuous monitor system |
WO2018100176A1 (en) | 2016-12-02 | 2018-06-07 | Metemis Development | Cartridge for biochemical sensor |
Families Citing this family (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8280476B2 (en) * | 2005-03-29 | 2012-10-02 | Arkal Medical, Inc. | Devices, systems, methods and tools for continuous glucose monitoring |
US20090131778A1 (en) * | 2006-03-28 | 2009-05-21 | Jina Arvind N | Devices, systems, methods and tools for continuous glucose monitoring |
US20100049021A1 (en) * | 2006-03-28 | 2010-02-25 | Jina Arvind N | Devices, systems, methods and tools for continuous analyte monitoring |
EP2989975B1 (en) | 2007-02-06 | 2018-06-13 | Medtronic MiniMed, Inc. | Optical systems and methods for rationmetric measurement of blood glucose concentration |
US8088097B2 (en) | 2007-11-21 | 2012-01-03 | Glumetrics, Inc. | Use of an equilibrium intravascular sensor to achieve tight glycemic control |
US7751863B2 (en) | 2007-02-06 | 2010-07-06 | Glumetrics, Inc. | Optical determination of ph and glucose |
US8738107B2 (en) | 2007-05-10 | 2014-05-27 | Medtronic Minimed, Inc. | Equilibrium non-consuming fluorescence sensor for real time intravascular glucose measurement |
EP2150814A2 (en) * | 2007-05-10 | 2010-02-10 | Glumetrics, Inc. | Device and methods for calibrating analyte sensors |
US20090024015A1 (en) * | 2007-07-17 | 2009-01-22 | Edwards Lifesciences Corporation | Sensing element having an adhesive backing |
US8396528B2 (en) * | 2008-03-25 | 2013-03-12 | Dexcom, Inc. | Analyte sensor |
WO2009129186A2 (en) | 2008-04-17 | 2009-10-22 | Glumetrics, Inc. | Sensor for percutaneous intravascular deployment without an indwelling cannula |
US20090270705A1 (en) * | 2008-04-28 | 2009-10-29 | Medtronic Minimed, Inc. | Automobile Physiological Monitoring System and Method for Using the Same |
US9119578B2 (en) | 2011-04-29 | 2015-09-01 | Seventh Sense Biosystems, Inc. | Plasma or serum production and removal of fluids under reduced pressure |
US9033898B2 (en) | 2010-06-23 | 2015-05-19 | Seventh Sense Biosystems, Inc. | Sampling devices and methods involving relatively little pain |
US9041541B2 (en) | 2010-01-28 | 2015-05-26 | Seventh Sense Biosystems, Inc. | Monitoring or feedback systems and methods |
US9295417B2 (en) | 2011-04-29 | 2016-03-29 | Seventh Sense Biosystems, Inc. | Systems and methods for collecting fluid from a subject |
JP6078230B2 (en) | 2009-03-02 | 2017-02-08 | セブンス センス バイオシステムズ,インコーポレーテッド | Techniques and devices related to blood sampling |
WO2011041546A1 (en) | 2009-09-30 | 2011-04-07 | Glumetrics, Inc. | Sensors with thromboresistant coating |
US8467843B2 (en) | 2009-11-04 | 2013-06-18 | Glumetrics, Inc. | Optical sensor configuration for ratiometric correction of blood glucose measurement |
US20120016308A1 (en) | 2010-07-16 | 2012-01-19 | Seventh Sense Biosystems, Inc. | Low-pressure packaging for fluid devices |
US20130158482A1 (en) | 2010-07-26 | 2013-06-20 | Seventh Sense Biosystems, Inc. | Rapid delivery and/or receiving of fluids |
WO2012021801A2 (en) | 2010-08-13 | 2012-02-16 | Seventh Sense Biosystems, Inc. | Systems and techniques for monitoring subjects |
EP2992827B1 (en) | 2010-11-09 | 2017-04-19 | Seventh Sense Biosystems, Inc. | Systems and interfaces for blood sampling |
US20120172692A1 (en) * | 2011-01-05 | 2012-07-05 | Janet Tamada | Sensing Fluid Concentration for Continuous Glucose Monitoring |
NO336532B1 (en) * | 2011-01-12 | 2015-09-21 | Mecsense As | Sensor for measuring the density of a body fluid and / or the resistance of a membrane |
EP2701600B1 (en) | 2011-04-29 | 2016-06-08 | Seventh Sense Biosystems, Inc. | Delivering and/or receiving fluids |
US20130158468A1 (en) | 2011-12-19 | 2013-06-20 | Seventh Sense Biosystems, Inc. | Delivering and/or receiving material with respect to a subject surface |
JP2014533523A (en) | 2011-09-02 | 2014-12-15 | ザ レジェンツ オブ ザ ユニヴァーシティー オブ カリフォルニア | Microneedle arrays for biosensing and drug delivery |
US8628724B2 (en) | 2012-01-03 | 2014-01-14 | Charleston Area Medical Center, Inc. | Integrated needle and test strip with aspiration apparatus and method of use |
US9451914B2 (en) | 2012-01-03 | 2016-09-27 | Charleston Area Medical Center, Inc. | Integrated needle and test strip assembly and method of use |
JP5713465B2 (en) * | 2012-09-14 | 2015-05-07 | 株式会社タニタ | Biosensor calibration method |
WO2014152717A2 (en) | 2013-03-14 | 2014-09-25 | Sano Intelligence, Inc. | On-body microsensor for biomonitoring |
US10820860B2 (en) | 2013-03-14 | 2020-11-03 | One Drop Biosensor Technologies, Llc | On-body microsensor for biomonitoring |
CN106456072A (en) * | 2014-03-12 | 2017-02-22 | 血糖测试仪股份有限公司 | Wearable electrochemical sensor and method |
CN106102578A (en) * | 2014-03-13 | 2016-11-09 | 萨诺智能公司 | For monitoring the system of body chemistry |
US10595754B2 (en) | 2014-03-13 | 2020-03-24 | Sano Intelligence, Inc. | System for monitoring body chemistry |
US9933387B1 (en) | 2014-09-07 | 2018-04-03 | Biolinq, Inc. | Miniaturized sub-nanoampere sensitivity low-noise potentiostat system |
WO2017160812A1 (en) * | 2016-03-16 | 2017-09-21 | Triax Technologies, Inc. | System and interfaces for managing workplace events |
US10878352B2 (en) | 2016-03-16 | 2020-12-29 | Triax Technologies, Inc. | Mesh based system and method for tracking worksite events experienced by workers via a wearable sensor |
US11810032B2 (en) | 2016-03-16 | 2023-11-07 | Triax Technologies, Inc. | Systems and methods for low-energy wireless applications using networked wearable sensors |
US11170616B2 (en) | 2016-03-16 | 2021-11-09 | Triax Technologies, Inc. | System and interfaces for managing workplace events |
US10769562B2 (en) | 2016-03-16 | 2020-09-08 | Triax Technologies, Inc. | Sensor based system and method for authorizing operation of worksite equipment using a locally stored access control list |
US10092207B1 (en) | 2016-05-15 | 2018-10-09 | Biolinq, Inc. | Tissue-penetrating electrochemical sensor featuring a co-electrodeposited thin film comprised of polymer and bio-recognition element |
KR101975198B1 (en) * | 2017-07-24 | 2019-08-28 | 최규동 | Hybride Continous Glucose Measuremrnt System |
CN109805940B (en) * | 2017-11-20 | 2022-07-12 | 研能科技股份有限公司 | Blood sugar monitoring control system |
US11478194B2 (en) | 2020-07-29 | 2022-10-25 | Biolinq Incorporated | Continuous analyte monitoring system with microneedle array |
USD988882S1 (en) | 2021-04-21 | 2023-06-13 | Informed Data Systems Inc. | Sensor assembly |
SE545874C2 (en) | 2021-05-08 | 2024-02-27 | Biolinq Incorporated | Fault detection for microneedle array based continuous analyte monitoring device |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998034541A1 (en) * | 1997-02-07 | 1998-08-13 | Abbott Laboratories | Apparatus for obtaining biological fluids |
US20030032000A1 (en) * | 2001-08-13 | 2003-02-13 | Signature Bioscience Inc. | Method for analyzing cellular events |
US20050171480A1 (en) * | 2003-11-21 | 2005-08-04 | The Regents Of The University Of California | Method and/or apparatus for puncturing a surface for extraction, in situ analysis, and/or substance delivery using microneedles |
US20060016700A1 (en) * | 2004-07-13 | 2006-01-26 | Dexcom, Inc. | Transcutaneous analyte sensor |
US20060219576A1 (en) * | 2005-03-29 | 2006-10-05 | Jina Arvind N | Devices, Systems, Methods And Tools For Continuous Glucose Monitoring |
Family Cites Families (92)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3964482A (en) * | 1971-05-17 | 1976-06-22 | Alza Corporation | Drug delivery device |
US4018938A (en) * | 1975-06-30 | 1977-04-19 | International Business Machines Corporation | Fabrication of high aspect ratio masks |
US4071020A (en) * | 1976-06-03 | 1978-01-31 | Xienta, Inc. | Apparatus and methods for performing in-vivo measurements of enzyme activity |
US4165395A (en) * | 1977-06-30 | 1979-08-21 | International Business Machines Corporation | Process for forming a high aspect ratio structure by successive exposures with electron beam and actinic radiation |
JPS5590931A (en) * | 1978-12-29 | 1980-07-10 | Canon Inc | Production of micro structure element array |
US4320758A (en) * | 1979-05-07 | 1982-03-23 | Alza Corporation | Osmotically driven fluid dispenser |
US4846950A (en) * | 1983-09-08 | 1989-07-11 | Montefiore Hospital Assn Of Western Pa | Cyclic controlled electrolysis apparatus |
US4821733A (en) * | 1987-08-18 | 1989-04-18 | Dermal Systems International | Transdermal detection system |
US5641504A (en) * | 1988-06-09 | 1997-06-24 | Alza Corporation | Skin permeation enhancer compositions using glycerol monolinoleate |
US5208147A (en) * | 1988-07-21 | 1993-05-04 | Radiometer A/S | Means for measuring a characteristic in a sample fluid |
US5438984A (en) * | 1988-09-08 | 1995-08-08 | Sudor Partners | Apparatus and method for the collection of analytes on a dermal patch |
US5096669A (en) * | 1988-09-15 | 1992-03-17 | I-Stat Corporation | Disposable sensing device for real time fluid analysis |
US5112455A (en) * | 1990-07-20 | 1992-05-12 | I Stat Corporation | Method for analytically utilizing microfabricated sensors during wet-up |
ATE176416T1 (en) * | 1990-11-21 | 1999-02-15 | Canon Kk | LASER PROCESSING DEVICE |
DE4222856C1 (en) * | 1992-07-11 | 1993-05-27 | Buerkert Gmbh | |
US5330634A (en) * | 1992-08-28 | 1994-07-19 | Via Medical Corporation | Calibration solutions useful for analyses of biological fluids and methods employing same |
JP2541081B2 (en) * | 1992-08-28 | 1996-10-09 | 日本電気株式会社 | Biosensor and method of manufacturing and using biosensor |
GB9320850D0 (en) * | 1993-10-09 | 1993-12-01 | Terwee Thomas H M | Monitoring the concentration of a substance or a group of substances in a body fluid of a human or an animal |
US5885211A (en) * | 1993-11-15 | 1999-03-23 | Spectrix, Inc. | Microporation of human skin for monitoring the concentration of an analyte |
US5458140A (en) * | 1993-11-15 | 1995-10-17 | Non-Invasive Monitoring Company (Nimco) | Enhancement of transdermal monitoring applications with ultrasound and chemical enhancers |
DE4401400A1 (en) * | 1994-01-19 | 1995-07-20 | Ernst Prof Dr Pfeiffer | Method and arrangement for continuously monitoring the concentration of a metabolite |
US6093520A (en) * | 1994-09-09 | 2000-07-25 | Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College | High aspect ratio microstructures and methods for manufacturing microstructures |
US5735273A (en) * | 1995-09-12 | 1998-04-07 | Cygnus, Inc. | Chemical signal-impermeable mask |
DE19618597B4 (en) * | 1996-05-09 | 2005-07-21 | Institut für Diabetestechnologie Gemeinnützige Forschungs- und Entwicklungsgesellschaft mbH an der Universität Ulm | Method for determining the concentration of tissue glucose |
ATE234129T1 (en) * | 1996-06-18 | 2003-03-15 | Alza Corp | DEVICE FOR IMPROVING TRANSDERMAL ADMINISTRATION OF MEDICATIONS OR EXTRACTION OF BODY FLUID |
US6139718A (en) * | 1997-03-25 | 2000-10-31 | Cygnus, Inc. | Electrode with improved signal to noise ratio |
US5747666A (en) * | 1997-03-26 | 1998-05-05 | Willis; John P. | Point-of-care analyzer module |
US5889856A (en) * | 1997-05-22 | 1999-03-30 | Centillium Technology Corp. | ADSL integrated line card with digital splitter and POTS CODEC without bulky analog splitter |
AU8031898A (en) * | 1997-06-16 | 1999-01-04 | Elan Medical Technologies Limited | Methods of calibrating and testing a sensor for (in vivo) measurement of an analyte and devices for use in such methods |
US5928207A (en) * | 1997-06-30 | 1999-07-27 | The Regents Of The University Of California | Microneedle with isotropically etched tip, and method of fabricating such a device |
SE9702739D0 (en) * | 1997-07-17 | 1997-07-17 | Siemens Elema Ab | Method for rinsing and calibrating sensors included in a body fluid analysis system |
US6223591B1 (en) * | 1997-11-28 | 2001-05-01 | Nikon Corporation | Probe needle arrangement and movement method for use in an atomic force microscope |
CA2313458C (en) * | 1997-12-11 | 2007-04-17 | Alza Corporation | Device for enhancing transdermal agent flux |
EP1045714A1 (en) * | 1998-01-08 | 2000-10-25 | Sontra Medical, L.P. | Sonophoretic enhanced transdermal transport |
US7066884B2 (en) * | 1998-01-08 | 2006-06-27 | Sontra Medical, Inc. | System, method, and device for non-invasive body fluid sampling and analysis |
SE9800693D0 (en) * | 1998-03-05 | 1998-03-05 | Siemens Elema Ab | A monitor for diffusable chemical substances |
CA2265119C (en) * | 1998-03-13 | 2002-12-03 | Cygnus, Inc. | Biosensor, iontophoretic sampling system, and methods of use thereof |
US6106751A (en) * | 1998-03-18 | 2000-08-22 | The Regents Of The University Of California | Method for fabricating needles via conformal deposition in two-piece molds |
US6175752B1 (en) * | 1998-04-30 | 2001-01-16 | Therasense, Inc. | Analyte monitoring device and methods of use |
US6233471B1 (en) * | 1998-05-13 | 2001-05-15 | Cygnus, Inc. | Signal processing for measurement of physiological analysis |
US6503231B1 (en) * | 1998-06-10 | 2003-01-07 | Georgia Tech Research Corporation | Microneedle device for transport of molecules across tissue |
US7344499B1 (en) * | 1998-06-10 | 2008-03-18 | Georgia Tech Research Corporation | Microneedle device for extraction and sensing of bodily fluids |
US6602678B2 (en) * | 1998-09-04 | 2003-08-05 | Powderject Research Limited | Non- or minimally invasive monitoring methods |
DE69913153D1 (en) * | 1998-09-17 | 2004-01-08 | Cygnus Therapeutic Systems | DEVICE FOR COMPRESSING A GEL / SENSOR UNIT |
WO2000064533A1 (en) * | 1999-04-22 | 2000-11-02 | Cygnus, Inc. | Methods and devices for removing interfering species |
US6546268B1 (en) * | 1999-06-02 | 2003-04-08 | Ball Semiconductor, Inc. | Glucose sensor |
US6743211B1 (en) * | 1999-11-23 | 2004-06-01 | Georgia Tech Research Corporation | Devices and methods for enhanced microneedle penetration of biological barriers |
US6379324B1 (en) * | 1999-06-09 | 2002-04-30 | The Procter & Gamble Company | Intracutaneous microneedle array apparatus |
US6256533B1 (en) * | 1999-06-09 | 2001-07-03 | The Procter & Gamble Company | Apparatus and method for using an intracutaneous microneedle array |
US6312612B1 (en) * | 1999-06-09 | 2001-11-06 | The Procter & Gamble Company | Apparatus and method for manufacturing an intracutaneous microneedle array |
US6406638B1 (en) * | 2000-01-06 | 2002-06-18 | The Regents Of The University Of California | Method of forming vertical, hollow needles within a semiconductor substrate, and needles formed thereby |
IL134997A0 (en) * | 2000-03-09 | 2001-05-20 | Yehoshua Yeshurun | Health care system based on micro device |
US6558361B1 (en) * | 2000-03-09 | 2003-05-06 | Nanopass Ltd. | Systems and methods for the transport of fluids through a biological barrier and production techniques for such systems |
WO2001088534A2 (en) * | 2000-05-16 | 2001-11-22 | Cygnus, Inc. | Methods for improving performance and reliability of biosensors |
US6565532B1 (en) * | 2000-07-12 | 2003-05-20 | The Procter & Gamble Company | Microneedle apparatus used for marking skin and for dispensing semi-permanent subcutaneous makeup |
US6603987B2 (en) * | 2000-07-11 | 2003-08-05 | Bayer Corporation | Hollow microneedle patch |
DE10038835B4 (en) * | 2000-08-04 | 2005-07-07 | Roche Diagnostics Gmbh | Microdialysis system |
US6533949B1 (en) * | 2000-08-28 | 2003-03-18 | Nanopass Ltd. | Microneedle structure and production method therefor |
US7108681B2 (en) * | 2000-10-16 | 2006-09-19 | Corium International, Inc. | Microstructures for delivering a composition cutaneously to skin |
US6638246B1 (en) * | 2000-11-28 | 2003-10-28 | Scimed Life Systems, Inc. | Medical device for delivery of a biologically active material to a lumen |
AU2904602A (en) * | 2000-12-11 | 2002-06-24 | Harvard College | Nanosensors |
GB0030929D0 (en) * | 2000-12-19 | 2001-01-31 | Inverness Medical Ltd | Analyte measurement |
US6591124B2 (en) * | 2001-05-11 | 2003-07-08 | The Procter & Gamble Company | Portable interstitial fluid monitoring system |
US6549796B2 (en) * | 2001-05-25 | 2003-04-15 | Lifescan, Inc. | Monitoring analyte concentration using minimally invasive devices |
US6875613B2 (en) * | 2001-06-12 | 2005-04-05 | Lifescan, Inc. | Biological fluid constituent sampling and measurement devices and methods |
US6721586B2 (en) * | 2001-06-12 | 2004-04-13 | Lifescan, Inc. | Percutaneous biological fluid sampling and analyte measurement devices and methods |
US7041068B2 (en) * | 2001-06-12 | 2006-05-09 | Pelikan Technologies, Inc. | Sampling module device and method |
US6767341B2 (en) * | 2001-06-13 | 2004-07-27 | Abbott Laboratories | Microneedles for minimally invasive drug delivery |
US6749792B2 (en) * | 2001-07-09 | 2004-06-15 | Lifescan, Inc. | Micro-needles and methods of manufacture and use thereof |
US6881203B2 (en) * | 2001-09-05 | 2005-04-19 | 3M Innovative Properties Company | Microneedle arrays and methods of manufacturing the same |
WO2003026732A2 (en) * | 2001-09-28 | 2003-04-03 | Biovalve Technologies, Inc. | Switchable microneedle arrays and systems and methods relating to same |
WO2003026733A2 (en) * | 2001-09-28 | 2003-04-03 | Biovalve Technologies, Inc. | Microneedle with membrane |
US6689100B2 (en) * | 2001-10-05 | 2004-02-10 | Becton, Dickinson And Company | Microdevice and method of delivering or withdrawing a substance through the skin of an animal |
US7399277B2 (en) * | 2001-12-27 | 2008-07-15 | Medtronic Minimed, Inc. | System for monitoring physiological characteristics |
US6908453B2 (en) * | 2002-01-15 | 2005-06-21 | 3M Innovative Properties Company | Microneedle devices and methods of manufacture |
US20030143746A1 (en) * | 2002-01-31 | 2003-07-31 | Sage Burton H. | Self-calibrating body anayte monitoring system |
US20030143113A2 (en) * | 2002-05-09 | 2003-07-31 | Lifescan, Inc. | Physiological sample collection devices and methods of using the same |
EP1590034B1 (en) * | 2002-10-07 | 2014-05-14 | Biovalve Technologies, Inc. | Microneedle array patch |
ATE433775T1 (en) * | 2002-10-11 | 2009-07-15 | Becton Dickinson Co | INSULIN DELIVERY SYSTEM WITH SENSOR |
US20060025717A1 (en) * | 2003-04-18 | 2006-02-02 | The Regents Of The University Of California | Method for forming hollow out-of-plane microneedles and devices formed hereby |
US7524464B2 (en) * | 2003-09-26 | 2009-04-28 | Ahn Chong H | Smart disposable plastic lab-on-a-chip for point-of-care testing |
ATE476909T1 (en) * | 2003-11-13 | 2010-08-15 | Medtronic Minimed Inc | LONG-TERM ANALYT SENSOR ARRANGEMENT |
WO2005066360A1 (en) * | 2003-12-05 | 2005-07-21 | Northwestern University | Micro/nano-fabricated glucose sensors using single-walled carbon nanotubes |
US8147426B2 (en) * | 2003-12-31 | 2012-04-03 | Nipro Diagnostics, Inc. | Integrated diagnostic test system |
US7076987B2 (en) * | 2004-08-05 | 2006-07-18 | Becton, Dickinson And Company | Method of producing tapered or pointed cannula |
US20060058602A1 (en) * | 2004-08-17 | 2006-03-16 | Kwiatkowski Krzysztof C | Interstitial fluid analyzer |
US7316665B2 (en) * | 2004-08-25 | 2008-01-08 | Becton, Dickinson And Company | Method and device for the delivery of a substance including a covering |
US7627938B2 (en) * | 2004-10-15 | 2009-12-08 | Board Of Regents, The Univeristy Of Texas System | Tapered hollow metallic microneedle array assembly and method of making and using the same |
US20060093658A1 (en) * | 2004-10-26 | 2006-05-04 | Gayatri Sathyan | Apparatus and method for transdermal delivery of desmopressin |
US20070004989A1 (en) * | 2005-06-29 | 2007-01-04 | Parvinder Dhillon | Device for transdermal sampling |
US20070066934A1 (en) * | 2005-09-19 | 2007-03-22 | Transport Pharmaceuticals, Inc. | Electrokinetic delivery system and methods therefor |
US7713196B2 (en) * | 2007-03-09 | 2010-05-11 | Nellcor Puritan Bennett Llc | Method for evaluating skin hydration and fluid compartmentalization |
-
2006
- 2006-12-20 US US11/642,196 patent/US20080154107A1/en not_active Abandoned
-
2007
- 2007-12-20 WO PCT/US2007/088456 patent/WO2008077147A2/en active Application Filing
- 2007-12-20 CA CA002670020A patent/CA2670020A1/en not_active Abandoned
- 2007-12-20 EP EP07865939A patent/EP2122309A2/en not_active Withdrawn
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998034541A1 (en) * | 1997-02-07 | 1998-08-13 | Abbott Laboratories | Apparatus for obtaining biological fluids |
US20030032000A1 (en) * | 2001-08-13 | 2003-02-13 | Signature Bioscience Inc. | Method for analyzing cellular events |
US20050171480A1 (en) * | 2003-11-21 | 2005-08-04 | The Regents Of The University Of California | Method and/or apparatus for puncturing a surface for extraction, in situ analysis, and/or substance delivery using microneedles |
US20060016700A1 (en) * | 2004-07-13 | 2006-01-26 | Dexcom, Inc. | Transcutaneous analyte sensor |
US20060219576A1 (en) * | 2005-03-29 | 2006-10-05 | Jina Arvind N | Devices, Systems, Methods And Tools For Continuous Glucose Monitoring |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009049243A2 (en) * | 2007-10-12 | 2009-04-16 | Arkal Medical, Inc. | Microneedle array with diverse needle configurations |
WO2009049243A3 (en) * | 2007-10-12 | 2009-05-28 | Arkal Medical Inc | Microneedle array with diverse needle configurations |
CN106236108A (en) * | 2016-08-30 | 2016-12-21 | 张胜国 | Intelligence Wicresoft blood glucose continuous monitor system |
WO2018100176A1 (en) | 2016-12-02 | 2018-06-07 | Metemis Development | Cartridge for biochemical sensor |
Also Published As
Publication number | Publication date |
---|---|
US20080154107A1 (en) | 2008-06-26 |
EP2122309A2 (en) | 2009-11-25 |
CA2670020A1 (en) | 2008-06-26 |
WO2008077147A3 (en) | 2008-10-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20080154107A1 (en) | Device, systems, methods and tools for continuous glucose monitoring | |
US20090099427A1 (en) | Microneedle array with diverse needle configurations | |
US7949382B2 (en) | Devices, systems, methods and tools for continuous glucose monitoring | |
US20080312518A1 (en) | On-demand analyte monitor and method of use | |
US20080234562A1 (en) | Continuous analyte monitor with multi-point self-calibration | |
US20100049021A1 (en) | Devices, systems, methods and tools for continuous analyte monitoring | |
US20090131778A1 (en) | Devices, systems, methods and tools for continuous glucose monitoring | |
EP2283770B1 (en) | Biological fluid constituent sampling and measurement devices and methods | |
EP1266608B1 (en) | Biological fluid sampling and analyte measurement device | |
US6990367B2 (en) | Percutaneous biological fluid sampling and analyte measurement devices and methods | |
EP2514362A1 (en) | Sensing fluid concentration for continuous glucose monitoring | |
JP2002528190A (en) | Kits and methods for quality control testing of iontophoretic sampling systems | |
US20170188898A1 (en) | Devices and methods for enhanced skin perforation for continuous glucose monitoring | |
US20110257497A1 (en) | Flux Enhancement in Continuous Glucose Monitoring | |
US20120172693A1 (en) | Pump Arrangement in Continuous Analyte Monitoring | |
WO2018226245A1 (en) | Devices and methods for enhanced skin perforation for continuous glucose monitoring |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 07865939 Country of ref document: EP Kind code of ref document: A2 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2670020 Country of ref document: CA |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2007865939 Country of ref document: EP |