US20100028207A1 - Cuvette-based apparatus for blood coagulation measurement and testing - Google Patents

Cuvette-based apparatus for blood coagulation measurement and testing Download PDF

Info

Publication number
US20100028207A1
US20100028207A1 US12/503,665 US50366509A US2010028207A1 US 20100028207 A1 US20100028207 A1 US 20100028207A1 US 50366509 A US50366509 A US 50366509A US 2010028207 A1 US2010028207 A1 US 2010028207A1
Authority
US
United States
Prior art keywords
channel
cuvette
blood
sampling
hydrophilic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/503,665
Inventor
Gregory M. Colella
Henry D. Huang
Anthony F. Kuklo, Jr.
Dimitri V. Shishkin
Maria Figueroa
James A. Mawhirt
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Instrumentation Laboratory Co
Original Assignee
International Technidyne Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by International Technidyne Corp filed Critical International Technidyne Corp
Priority to US12/503,665 priority Critical patent/US20100028207A1/en
Assigned to INTERNATIONAL TECHNIDYNE CORPORATION reassignment INTERNATIONAL TECHNIDYNE CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: COLELLA, GREGORY M., KUKLO, ANTHONY F., JR., FIGUEROA, MARIA, HUANG, HENRY D., MAWHIRT, JAMES A., SHISHKIN, DIMITRI
Publication of US20100028207A1 publication Critical patent/US20100028207A1/en
Assigned to COMERICA BANK reassignment COMERICA BANK INTELLECTUAL PROPERTY SECURITY AGREEMENT Assignors: INTERNATIONAL TECHNIDYNE CORPORATION
Priority to US13/474,243 priority patent/US20130017126A1/en
Priority to US13/959,007 priority patent/US10180419B2/en
Assigned to INTERNATIONAL TECHNIDYNE CORPORATION reassignment INTERNATIONAL TECHNIDYNE CORPORATION RELEASE BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: COMERICA BANK
Assigned to INSTRUMENTATION LABORATORY COMPANY reassignment INSTRUMENTATION LABORATORY COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: INTERNATIONAL TECHNIDYNE CORPORATION
Priority to US16/210,433 priority patent/US10578605B2/en
Priority to US16/805,375 priority patent/US11402369B2/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/49Blood
    • G01N33/4905Determining clotting time of blood
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/502715Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/502723Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by venting arrangements
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/50273Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the means or forces applied to move the fluids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/12Specific details about manufacturing devices
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/14Process control and prevention of errors
    • B01L2200/143Quality control, feedback systems
    • B01L2200/146Employing pressure sensors
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/16Reagents, handling or storing thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/02Identification, exchange or storage of information
    • B01L2300/025Displaying results or values with integrated means
    • B01L2300/027Digital display, e.g. LCD, LED
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/06Auxiliary integrated devices, integrated components
    • B01L2300/0627Sensor or part of a sensor is integrated
    • B01L2300/0654Lenses; Optical fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/08Geometry, shape and general structure
    • B01L2300/0809Geometry, shape and general structure rectangular shaped
    • B01L2300/0816Cards, e.g. flat sample carriers usually with flow in two horizontal directions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/08Geometry, shape and general structure
    • B01L2300/0861Configuration of multiple channels and/or chambers in a single devices
    • B01L2300/0864Configuration of multiple channels and/or chambers in a single devices comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/16Surface properties and coatings
    • B01L2300/161Control and use of surface tension forces, e.g. hydrophobic, hydrophilic
    • B01L2300/165Specific details about hydrophobic, oleophobic surfaces
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00Moving or stopping fluids
    • B01L2400/04Moving fluids with specific forces or mechanical means
    • B01L2400/0475Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure
    • B01L2400/0487Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure fluid pressure, pneumatics
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00Moving or stopping fluids
    • B01L2400/08Regulating or influencing the flow resistance
    • B01L2400/084Passive control of flow resistance
    • B01L2400/086Passive control of flow resistance using baffles or other fixed flow obstructions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/502746Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the means for controlling flow resistance, e.g. flow controllers, baffles
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/49Blood
    • G01N33/4915Blood using flow cells

Definitions

  • the invention relates to apparatus and methods for measuring and testing blood coagulation. More particularly, the invention relates to a cuvette-based apparatus for blood coagulation measurement and testing having automatic volumetric blood sample filling capability.
  • the peak anticoagulant effect of the anticoagulant may be delayed by many hours and/or days, and the duration of the effect may persist after the peak for another four to five days. Accordingly, it is critical that the people who take anticoagulants closely monitor the coagulation time of their blood, so that they can monitor and adjust the amount of the anticoagulant they are taking.
  • a common manner of determining the effective amount of anticoagulant in a person's blood is to perform a prothrombin time (PT) test.
  • PT prothrombin time
  • a PT test measures how long a sample of blood takes to clot.
  • the anticoagulation or hemostasis level in the blood is directly proportional to the length of time required to form clots.
  • a problem associated with such apparatus is that the volume of the blood sample drawn into the cuvette for measurement and testing is controlled by both the testing device and the sample cup removal techniques. Moreover, the cup-like supply reservoir can be messy to use.
  • a cuvette is described herein for use with a blood clot detection instrument.
  • the cuvette comprises a blood sample receptor-inlet and a channel arrangement comprising: at least one test channel for performing a blood clotting time measurement; a sampling channel communicating with the blood sample receptor-inlet and the at least one test channel; a waste channel communicating with the sampling channel; and a vent opening communicating with the sampling channel.
  • At least the sampling channel and the waste channel each has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic.
  • the sampling channel with its at least one surface portion that is hydrophilic, the vent opening and the waste channel with its at least one surface portion that is hydrophilic coact to automatically draw a requisite volume of a blood sample deposited at the blood receptor-inlet, into the sampling channel. More specifically, air compressed within the blood clot detection instrument, the at least one test channel of the cuvette, and the section of the sampling channel extending beyond the vent opening of the cuvette, coacts with the waste channel to cause the a leading edge of the blood sample drawn into the sampling channel from the blood receptor-inlet, to pull back within the sampling channel and uncover an optical sensor of the blood clot detection instrument.
  • the volume of the blood sample in the sampling channel at the time when the blood sample is pulled back to uncover the optical sensor equals the requisite volume.
  • the uncovering of the optical sensor activates a pump module of the blood clot detection instrument, which draws the requisite volume of the blood sample into the at least one test channel.
  • the apparatus comprises: a blood clot detection instrument and a cuvette for use with the blood clot detection instrument.
  • the blood clot detection instrument comprises: a pump module and at least one pressure sensor.
  • the cuvette comprises a blood sample receptor-inlet; a channel arrangement comprising: at least one test channel for performing a blood clotting time measurement; a sampling channel communicating with the blood sample receptor-inlet and the at least one test channel; and a waste channel communicating with the sampling channel; and a vent opening communicating with the sampling channel.
  • At least the sampling channel has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic.
  • the sampling channel with its at least one surface portion that is hydrophilic, the vent opening and the waste channel coact to automatically draw a requisite volume of a blood sample deposited at the blood receptor-inlet, into the sampling channel, the requisite volume of blood sample being drawn into the at least one test channel when the pump module of the blood clot detection instrument is activated.
  • the at least one test channel of the cuvette, and the pump module and the at least one pressure sensor of the clot detection instrument coact to perform a blood clotting time measurement on the requisite volume of the blood sample.
  • the blood clot detection instrument for automatically measuring blood clotting time of a blood sample contained in a test channel of a cuvette.
  • the blood clot detection instrument comprises a pump module for communicating with the test channel of the cuvette; a pressure sensor; and a central processing unit.
  • the central processing unit executes instructions for operating the pump module in a pressure alternating mode that pumps the blood sample back and forth in a test channel of a cuvette.
  • the viscosity of the blood sample increases and causes a pumping pressure of the pump module to increase over time.
  • the central processing unit executes further instructions for obtaining a baseline pumping pressure from the pressure sensor upon initial operation of the pump module in the pressure alternating mode; obtaining additional pumping pressures over time from the pressure sensor; determining a pumping pressure difference value between each additional pumping pressure and the baseline pumping pressure; comparing each pumping pressure difference value to a predetermined threshold value; and indicating the blood clotting time of the blood sample when the pumping pressure difference value exceeds the predetermined threshold value, the indicated blood clotting time comprising a duration of time extending between the measurement of the additional pumping pressure used for determining the pumping pressure difference value that exceeded the predetermined threshold value and the measurement of the baseline pumping pressure.
  • FIG. 1 is a schematic view of an embodiment of a cuvette-based apparatus for measuring blood coagulation or clotting time.
  • FIG. 2A is a schematic plan view of an embodiment of the disposable cuvette.
  • FIG. 2B is a sectional view through line 2 B- 2 B of FIG. 2A .
  • FIG. 2C is a sectional view through line 2 C- 2 C of FIG. 2A .
  • FIG. 3A is an enlarged view of a blood sample testing portion of the disposable cuvette shown in FIG. 2A .
  • FIG. 3B is a section view through line 3 B- 3 B of FIG. 3A .
  • FIG. 4 is an enlarged view of a volumetric blood sampling portion of the disposable cuvette shown in FIG. 2A .
  • FIG. 5 is a pressure profile and clot detection graph.
  • FIG. 6A is a schematic plan view of another embodiment of the disposable cuvette.
  • FIG. 6B is a schematic plan view of a further embodiment of the disposable cuvette.
  • FIG. 7A is a perspective view of a further embodiment of the disposable cuvette.
  • FIG. 7B is an enlarged view of encircled area 7 B in FIG. 7A .
  • FIG. 7C is a sectional view through line 7 C- 7 C in FIG. 7B .
  • FIG. 1 there is shown a schematic view of an embodiment of a cuvette-based apparatus 10 for measuring blood coagulation or clotting time.
  • the apparatus 10 generally comprises a disposable cuvette 100 and a blood clot detection instrument 200 .
  • the apparatus 10 may be used for measuring blood coagulation time by depositing a sample of blood (whole blood or plasma) onto a specified location of the disposable cuvette 100 and operatively coupling the disposable cuvette 100 to the clot detection instrument 200 .
  • the cuvette 100 automatically selects or fills itself with a requisite volume of the blood sample (to be tested) deposited at the specified location of the cuvette 100 .
  • the clot detection instrument 200 facilitates automatic mixing of the blood sample with a clotting reagent within the cuvette 100 and automatically measures the clotting time of the selected volume of the blood sample mixed with the clotting reagent within the disposable cuvette 100 , without contacting the blood sample. After completion of the measurement, the cuvette 100 may be uncoupled or removed from the clot detection instrument 200 and disposed of. Because the clot detection instrument 200 does not contact the blood sample, another cuvette 100 may be operatively coupled to the clot detection instrument 200 for measuring another blood sample without sterilization or other cleaning of the clot detection instrument 200 .
  • the clot detection instrument 200 comprises a pneumatic pump module 210 , a motor 220 for driving the pump module 210 , a plurality of tubes 230 extending from the pump module 210 for pneumatically coupling with the cuvette 100 , a pressure sensor 240 associated with each tube 230 for measuring the pneumatic pressure within the tube 230 , and an optical sensor 250 for optically sensing a sampling channel in the cuvette 100 .
  • the optical sensor 250 comprises, but is not limited, to a LED/photo sensor.
  • the clot detection instrument 200 also comprises, without limitation, a central processing unit 260 (CPU) executing instructions for controlling the operation of the motor 220 and thus the pump module 220 via signals received from the optical sensor 250 , and determining clotting time based on the pressures sensed by the pressure sensors 240 , a display (not shown) for displaying the measured clotting time or other data related to the measurement, a memory 270 for storing previously performed measurements, and buttons, knobs, and/or switches (not shown) for operating the clot detection instrument 200 , controlling the display and/or accessing stored data from the memory 270 .
  • CPU central processing unit
  • the cuvette 100 comprises a substantially planar main body 110 defining generally planar top and bottom surfaces 111 , 112 .
  • the cuvette main body 110 is typically made from a rigid, transparent hydrophobic or hydrophilic plastic material, using any suitable forming method, such molding.
  • the plastic hydrophobic materials may include, without limitation polystyrene and polytetrafluoroethylene and the plastic hydrophilic materials may include, without limitation, styrene acrylonitrile, acrylonitrile styrene acrylate.
  • the cuvette main body 110 may also be made from other types of rigid, transparent hydrophobic or hydrophilic materials.
  • the cuvette main body 110 includes an arrangement of open channels formed in its bottom surface 112 .
  • the open channels are covered and sealed by a thin, substrate 120 that is non-removably attached to the bottom surface 112 of the cuvette body 110
  • the channels of the channel arrangement each have at least one surface that is hydrophilic, and/or has a hydrophilic coating, and/or has a hydrophilic insert disposed therein (formed, for example, as a tube or liner, thereby fully or partially lining the channel(s)), that facilitates the automatic filling function of the cuvette 100 .
  • At least a top surface 121 of the thin substrate 120 i.e., the surface in contact with the bottom surface 112 of the cuvette body 110 , is hydrophilic or has hydrophilic properties.
  • the hydrophilic properties of the top surface 121 of the substrate 120 facilitates the requisite volumetric selection of the blood sample deposited on the cuvette 100 , for coagulation time measurement by the clot detection instrument 200 .
  • requisite volumetric selection of the blood sample is accomplished by forming the cuvette body 110 from a hydrophilic material.
  • the thin substrate 120 in one embodiment, is a transparent film 122 coated on one side with a layer 122 a of clear pressure sensitive hydrophilic adhesive.
  • the layer 122 a of hydrophilic adhesive forms the top surface 121 of the substrate 120 and non-removably attaches the substrate 120 to the bottom surface 112 of the cuvette body 110 .
  • the transparent film 122 may comprise, in one embodiment, a transparent polyester material.
  • the transparent film 122 is made from a hydrophilic material.
  • a substrate may be attached to the bottom surface 112 of the cuvette body 110 (with the top surface 121 of the substrate 120 mated with the bottom surface 112 of the cuvette body 110 ) with a layer of adhesive applied to the bottom surface 112 of cuvette body 110 .
  • such a substrate may be attached to the bottom surface 112 of the cuvette body 110 using heat sealing methods.
  • the channel arrangement formed in the bottom surface of the cuvette body 110 generally comprises a sampling channel 130 , one or more test channels 140 and at least one waste channel 150 .
  • a first end 131 of the sampling channel 130 communicates with a sample depositing area 160 formed in a first or front end 113 of the cuvette body 110 .
  • the sample depositing area 160 in the front end 113 of the cuvette body 110 and the exposed underlying portion of the substrate 120 form a blood sample receptor and inlet 161 (receptor-inlet 161 ) on which the entire blood sample is deposited.
  • the sampling channel 130 extends longitudinally in the bottom surface of the cuvette body 110 , from the receptor-inlet 161 , and merges at its second end with the one or more test channels 140 formed in the bottom surface of the cuvette body 110 .
  • the channel arrangement shown in FIGS. 2A-2C further includes a jumper channel 170 that branches off from the sampling channel 130 just downstream of the receptor-inlet 161 and fluidly connects the waste channel 150 with the sampling channel 130 .
  • the terminal end of the waste channel 150 communicates with a waste channel venting aperture 151 formed transversely through the cuvette body 110 , which allows “dead” air displaced from within the waste and jumper channels 150 , 170 by incoming blood, to be vented to the external environment.
  • the waste channel venting aperture 151 is open to the external environment at the top surface 111 of the cuvette body 110 and closed by the substrate 120 at the bottom surface of the cuvette body 110 .
  • the channel arrangement shown in FIGS. 2A-2C further includes a vent channel 180 that branches off from the sampling channel 130 downstream of the jumper channel 170 .
  • the vent channel 180 communicates with a vent opening 181 formed transversely through the cuvette body 110 which allows “dead” air displaced from within the sampling and vent channels 130 , 180 by incoming blood to be vented to the external environment.
  • the vent opening 181 is open to the external environment at the top surface 111 of the cuvette body 110 and closed by the substrate 120 at the bottom surface of the cuvette body 110 .
  • the sampling channel 130 (and the jumper, waste and vent channels 170 , 150 , 180 ) formed in the bottom surface 112 of the cuvette main body 110 has a smooth top T surface and smooth side surfaces S.
  • the bottom surface B of the sampling channel 130 (and the jumper, waste and vent channels 170 , 150 , 180 ) is formed by the top surface 121 (e.g., hydrophilic adhesive layer 122 a or the top surface of the hydrophilic film 122 ) of the substrate 120 , which is also smooth.
  • the cuvette main body 110 is made from a hydrophobic material.
  • the sampling, vent, jumper, and waste channels 130 , 180 , 170 , and 150 respectively, each includes at least one surface that is hydrophilic, and/or has a hydrophilic coating, and/or has a hydrophilic insert disposed therein, that facilitates the automatic sample sizing function of the cuvette 100 .
  • the cuvette main body 110 is made from a hydrophilic material.
  • the one or more test channels 140 in such embodiments each includes at least one surface that is hydrophobic, and/or has a hydrophobic coating, and/or has a hydrophobic insert disposed therein, where no automatic filling or sample sizing function is required to be performed by the cuvette 100 .
  • the requisite volume of blood sample selected by the cuvette 100 for measurement by the clot detection instrument 200 is obtained from the blood sample deposited on the receptor-inlet 161 .
  • the size of this volume is determined by the effective volume of the sampling channel 130 .
  • the effective volume of the sampling channel 130 is determined by the width of the sampling channel 130 , the height of the sampling channel 130 , and length of the sampling channel 130 as measured from point A, which is adjacent to the receptor-inlet 161 , to point B, which is adjacent to the vent channel 180 .
  • the jumper channel 170 connecting the sampling channel 130 to waste channel 150 , delays the filling of the waste channel 150 until the sampling channel 130 is completely filled.
  • the duration of the delay is controlled by an intersection I of the jumper channel 170 and the waste channel 150 and the length and cross-sectional area (CSA) of jumper channel 170 relative to the CSA of the waste channel 150 , which insure that blood from the blood sample deposited on the receptor-inlet 161 , is drawn into the sampling channel 130 prior to being drawn into the waste channel 150 .
  • the delay time is determined by the cross section area and length of the jumper channel 170 .
  • the duration of the delay may be increased by lengthening the jumper channel 170 , and/or decreasing the cross-sectional area (width and height) of the jumper channel 170 relative to the CSA of the waste channel to increase flow resistant through the jumper channel 170 .
  • the intersection I of the jumper channel 170 and the waste channel 150 acts like a resistor.
  • the blood sample Once a blood sample is applied or deposited in the cuvette's receptor-inlet 161 , the blood sample enters the sampling channel 130 and the jumper channel 170 substantially simultaneously. While the blood sample moves forward in the sampling channel 130 , it also fills the jumper channel 170 , then stops at the intersection I of the jumper channel 170 and the waste channel 150 . The sampling channel 130 continues to fill until an equilibrium state is reached. The remaining sample in the receptor-inlet 161 then forces the blood sample into the waste channel 150 from the jumper channel 170 . The hydrophilic force of the waste channel 150 picks up and draws off the remaining blood sample in the receptor-inlet 161 .
  • the sampling channel 130 has a width of about 0.055 inches, a height of about 0.014 inches, and a length of about 0.9 inches;
  • the vent channel 180 has a width of about 0.010 inches, a height of about 0.012 inches, and a length of about 0.140 inches;
  • the jumper channel 170 has a width of about 0.010 inches, a height of about 0.012 inches, and a length of about 0.25 inches;
  • the waste channel 150 has a width of about 0.066 inches, a height of about 0.014 inches, and length of about 2.24 inches.
  • the three test channels 140 of such a cuvette each has a width of about 0.030 inches and a height of about 0.010 inches.
  • the length of each of the outer two test channels is about 1.69 inches and the inner test channel is about 1.634 inches.
  • the sampling, jumper, waste, and test channel(s) in other embodiments of the cuvette may have other suitable dimensions.
  • FIG. 6A shows an another embodiment of the cuvette, denoted by reference number 300 .
  • the cuvette 300 is substantially identical to the cuvette 100 shown in FIG. 2A , except that the vent channel extending between the sampling channel and the vent opening is replaced by a vent opening 381 that directly opens into the sampling channel 130 .
  • FIG. 6B shows a further embodiment of the cuvette, denoted by reference number 400 .
  • the cuvette 400 is substantially identical to the cuvette 100 shown in FIG. 2A , except that the waste channel 450 communicates directly with the sampling channel 130 thereby omitting the jumper channel.
  • the waste channel 450 includes one or more restrictions 452 located just after the entrance to the waste channel 450 that function to delay filing of the waste channel 450 .
  • FIGS. 7A-7C collectively show a further embodiment of a cuvette, denoted by reference number 500 .
  • the cuvette 500 is substantially identical to the cuvette 100 shown in FIG. 2A , except that the one or more open test channels 140 are formed in the top surface 111 of the main body 110 instead of in the bottom surface 112 of the main body 110 where the open sampling, vent, jumper, and waste channels 130 , 180 , 170 , 150 are formed.
  • the open one or more test channels 140 in the top surface 111 of the cuvette main body 110 are covered and sealed by a thin substrate 530 with hydrophobic properties (e.g., the substrate 530 includes a hydrophobic adhesive coating or is a hydrophobic film) that is non-removably attached to the top surface 111 of the cuvette main body 110
  • the open sampling, vent, jumper, and waste channels 130 , 180 , 170 , 150 in the bottom surface 112 of the cuvette main body 110 are covered and sealed by a thin, substrate 520 with hydrophilic properties (e.g., the substrate 520 includes a hydrophilic adhesive coating or is a hydrophilic film) that is non-removably attached to the bottom surface 112 of the cuvette body 110 .
  • a connecting channel 550 formed in the top surface 111 of the cuvette main body 110 has a first end 550 a that communicates with a terminal end of the sampling channel 103 and a second end 550 b that communicates with an inlet 540 to the one or more test channels 140 .
  • the first end 550 a of the connecting channel 550 is covered and sealed by the hydrophillic substrate 520 .
  • the remainder of the connecting channel 550 including the second end 550 b thereof, is covered and sealed by the hydrophobic substrate 530 .
  • the connecting channel 550 transfers the volume of the blood sample precisely collected by the sampling channel 130 , to the one or more test channels 140 .
  • the one or more test channels 140 comprises a branched array of three test channels 140 in a menorah-shaped configuration 140 m (visible in FIGS. 2A , 3 A, 4 , 6 A and 6 B).
  • the menorah-shaped array of test channels 140 m evenly divides the selected volume of blood into three separate blood samples, thereby allowing the cuvette 100 to be used for performing up to three different blood tests.
  • the blood tests that may be performed in the cuvette, see U.S. Pat. No. 5,534,226, entitled, PORTABLE TEST APPARATUS AND ASSOCIATED METHOD OF PERFORMING A BLOOD COAGULATION TEST, assigned to the International Technidyne Corporation, the assignee herein.
  • the entire disclosure of U.S. Pat. No. 5,534,226 is incorporated herein by reference.
  • the branched array in other embodiments of the cuvette 100 may include two test channels 140 or more than three test channels 140 .
  • each test channel 140 communicates with a drive aperture 141 formed through the cuvette body 110 .
  • the drive aperture 141 is open to the external environment at the top surface 112 of the cuvette body 110 and closed by the substrate 120 at the bottom surface of the cuvette body 110 .
  • each of the test channels 140 formed in the bottom surface of the cuvette body 110 includes end sections 142 a with smooth top, side and bottom walls (the bottom wall of each test channel 140 being formed by the smooth top surface 121 of the substrate 120 ) similar to the top, side and bottom walls of the sampling, jumper and waste channels 130 , 170 , and 150 , and an intermediate section 142 b where the top wall T T and side walls S T are textured.
  • the texturing may comprise a flat knurl cross-hatch.
  • the texturing in the intermediate section 142 b of one or more of test channels 140 may only be on the top wall or on one or both of the side walls.
  • the length of the textured section is selected so that the blood sample BLD always remains within this section of the test channel 140 during testing.
  • a dehydrated clot promoting reagent (not shown) for triggering and accelerating blood clotting, is disposed in each test channel 140 where the texturing is located.
  • the reagent in each test channel 140 may be the same or different. Therefore, in one embodiment, reagent A may be in each of the test channels. In another embodiment, reagent A may be in two of the test channels and reagent B may be in one of the test channels. In still another embodiment, reagent A may be in one of the test channels, reagent B may be in one of the test channels and reagent C may be in one of the test channels.
  • each test channel 140 improves reagent deposition thereon during manufacture of the cuvette, and increase clotting measurement sensitivity, as the blood sample is reciprocally moved or oscillated therein when measuring of the clotting time of the blood sample, as will be explained further on.
  • the textured intermediate section of one or more the test channels 140 may be replaced by a restricted area (not shown) where the test channel 140 is narrowed.
  • the automatic volumetric filling function of the cuvette 100 will now be described in greater detail with reference to FIG. 4 .
  • the cuvette 100 Prior to volumetric filling, the cuvette 100 must be operatively coupled to the clot detection instrument 200 such that the plurality of tubes 230 extending from the pump module 210 of the clot detection instrument 200 sealingly engage the one or more drive apertures 141 of the cuvette body 110 , thereby creating a pneumatic system formed by the arrangement of channels of the cuvette 100 and the pneumatic pump module 210 of the clot detection instrument 200 , as shown in FIG. 1 .
  • the automatic volumetric filling function commences when a blood sample is deposited onto the receptor-inlet 161 of the cuvette 100 .
  • the blood sample may be deposited on the receptor-inlet 161 by finger after a fingerstick, a needle, a dropper, a pipette, a capillary tube, or any other suitable depositing device. Since at least a portion of the sampling channel 130 is hydrophilic, a force F s is generated by the hydrophilicity of this portion, which initially draws the blood sample deposited on the receptor-inlet 161 into the sampling channel 130 until the entire vent channel 180 becomes filled. The dead air in the vent channel 180 and the section of the sampling channel 130 extending between the receptor-inlet 161 and the vent channel 180 , is vented through the vent opening 181 of the vent channel 180 as the blood BLD fills this section of the sampling channel 130 , and the vent channel 180 .
  • the blood drawn into the vent channel 180 seals the vent opening 181 .
  • the jumper channel hydrophilicity force F j draws blood into the jumper channel.
  • the force F s continues to draw more blood from the blood sample deposited on the receptor-inlet 161 into the sampling channel 130 such that the blood BLD in the sampling channel 130 overshoots the vent channel 180 and covers the optical sensor 250 of the clot detection instrument 200 , which lies under or over section or area 131 of the sampling channel 130 .
  • the waste channel 150 After the equilibrium state has been reached, blood that has been delayed by the the jumper channel/waste channel intersection I and the jumper channel 170 , reaches the waste channel 150 .
  • the waste channel 150 generates a force F w , that increases to a value proportional to the line of contact between the blood and the hydrophilic surface, which first pulls additional blood remaining in the receptor-inlet 161 into the waste channel 150 .
  • F w As the waste channel 150 fills with excess blood sample BLD, dead air disposed therein and displaced by the incoming blood BLD is vented to the external environment through the waste channel venting aperture 151 .
  • force F w +F p becomes greater than F s , and therefore, the leading edge E of the blood BLD in the sampling channel 130 starts pulling back towards the vent channel 180 .
  • the leading edge E of the blood BLD in the sampling channel 130 continues to be pulled back by force F w +F p and uncovers the optical sensor 250 .
  • the volume of the blood sample BLD disposed in the sampling channel 130 at the moment the optical sensor 250 is uncovered, is the requisite volume. Consequently, the pump module 210 of the clot detection instrument 200 is immediately activated by the uncovered optical sensor 250 and draws this requisite volume of blood sample BLD into the test channels 140 such that the blood sample BLD is disposed in the sections of the test channels 140 that are textured.
  • the ratio of force F w to force F s determines the sample pull back speed. Generally, a wider waste channel 150 has stronger pull back.
  • the ratio of force F w to force F s equals 1.2.
  • the forces described above may be adjusted by the material properties of the cuvette body 110 , substrate 120 , size and/or geometry of the plurality of channels.
  • the blood sample over shoot and pull back functions of the sampling channel 130 may also be adjusted and controlled by the volume of dead air in the tubes 230 and pump module 210 of the clot detection instrument 200 .
  • the automatic blood clot testing function of the cuvette 100 will now be described in greater detail with reference to FIGS. 3A and 5 .
  • the pump module 210 automatically switches into a pumping mode where it alternately creates positive and negative pressures in the test channels 140 of the cuvette 100 .
  • the alternating positive and negative pressures reciprocally moves the blood samples BLD back and forth across textured sections (or restricted areas) of the one or more test channels 140 , thereby mixing the blood sample with dehydrated reagent, as shown in FIG. 3A .
  • the reagent rehydrates and mixes with the blood sample BLD, it triggers and accelerates the blood clotting cascade.
  • Fibrin formation within the blood sample BLD causes the viscosity of the blood sample BLD to increase with time.
  • the viscosity increase may be detected, in one embodiment, by measuring the pumping pressure within each test channel 140 over time. As shown in the graph of FIG. 5 , the pumping pressure starts at an initial pumping pressure value (pumping pressure baseline ⁇ P baseline ) and increases with time, as the viscosity of the blood increases during clotting.
  • the pressure sensors 240 of the blood clot detection instrument 200 measure the pump pressure over time and the CPU 260 of the clot detection instrument 200 compares this data to the initial pressure baseline ⁇ P baseline .
  • the clotting time of the blood sample may be determined when pressure value is greater than or equal to a preset threshold. In one embodiment, the clotting time is,
  • ⁇ P end point is the clotting end point peak to peak pressure
  • the preset threshold may be fixed or dynamic.
  • a dynamic threshold may be,
  • the hydrophilicity of the one or more test channels 140 will aid the robust automatic volumetric blood sample filling function of the cuvette 100 , while impeding the clotting performance of the cuvette 100 .
  • Appropriately balancing the test channel 140 dimensions, geometry, degree of texturing/restriction size, and the hydrophilic properties of the cuvette body 110 and substrate 120 will provide the cuvette 100 with requisite blood clotting performance.
  • the pump profile of the pump module 210 may also affect clotting performance. For example, a pump speed greater than 20 millisecond (ms) per pump step, equivalent to 20 ul per sec in test channel or a pump stroke greater than 55 steps, equivalent to 0.044, may increase the chance of deforming a weak clot (International Normalized Ratio>4.0), which may in turn, result in lower clot detection precision.
  • the pump profile is 40 ms per pump step and 36 steps per pump direction (generates positive and negative pressures).

Abstract

An apparatus for measuring blood clotting time includes a blood clot detection instrument and a cuvette for use with the blood clot detection instrument. The cuvette includes a blood sample receptor-inlet; a channel arrangement including at least one test channel for performing a blood clotting time measurement, a sampling channel having at least one surface portion that is hydrophilic, communicating with the blood sample receptor-inlet and the at least one test channel, and a waste channel having at least one surface portion that is hydrophilic, communicating with the sampling channel; and a vent opening communicating with the sampling channel. The sampling channel, the vent opening and the waste channel, coact to automatically draw a requisite volume of a blood sample deposited at the blood receptor-inlet, into the sampling channel. More specifically, air compressed within the blood clot detection instrument, the at least one test channel of the cuvette, and the section of the sampling channel extending beyond the vent opening of the cuvette, coacts with the waste channel to cause a leading edge of the blood sample drawn into the sampling channel from the blood receptor-inlet, to pull back within the sampling channel and uncover an optical sensor in of the blood clot detection instrument. The uncovering of the optical sensor activates a pump module of the blood clot detection instrument, which draws the requisite volume of the blood sample into the at least one test channel.

Description

    RELATED APPLICATIONS
  • This application claims the benefit of U.S. Provisional Application No. 61/081,290, filed Jul. 16, 2008, the entire disclosure of which is incorporated herein by reference.
  • FIELD
  • The invention relates to apparatus and methods for measuring and testing blood coagulation. More particularly, the invention relates to a cuvette-based apparatus for blood coagulation measurement and testing having automatic volumetric blood sample filling capability.
  • BACKGROUND
  • Many people take anticoagulants to maintain the theropedic coagulation time of their blood. Depending upon the person, the peak anticoagulant effect of the anticoagulant may be delayed by many hours and/or days, and the duration of the effect may persist after the peak for another four to five days. Accordingly, it is critical that the people who take anticoagulants closely monitor the coagulation time of their blood, so that they can monitor and adjust the amount of the anticoagulant they are taking.
  • A common manner of determining the effective amount of anticoagulant in a person's blood is to perform a prothrombin time (PT) test. A PT test measures how long a sample of blood takes to clot. As a result, the anticoagulation or hemostasis level in the blood is directly proportional to the length of time required to form clots.
  • Many devices and apparatus exist for performing coagulation time measurements and tests. Some of these apparatus are portable and simple enough to operate by a person in his or her home. An example of such an apparatus is describe in U.S. Pat. No. 5,534,226, entitled PORTABLE TEST APPARATUS AND ASSOCIATED METHOD OF PERFORMING A BLOOD COAGULATION TEST, issued to Gavin et al. and assigned to International Technidyne Corporation, the assignee herein. The apparatus described in this patent includes a disposable cuvette and a testing device. In operation, a sample of blood is placed into a cup-like supply reservoir of the cuvette, the blood sample is drawn into the cuvette, and the coagulation time of the blood sample is measured.
  • A problem associated with such apparatus, is that the volume of the blood sample drawn into the cuvette for measurement and testing is controlled by both the testing device and the sample cup removal techniques. Moreover, the cup-like supply reservoir can be messy to use.
  • Accordingly, a need exits for an improved apparatus for measuring and testing blood coagulation.
  • SUMMARY
  • A cuvette is described herein for use with a blood clot detection instrument. The cuvette comprises a blood sample receptor-inlet and a channel arrangement comprising: at least one test channel for performing a blood clotting time measurement; a sampling channel communicating with the blood sample receptor-inlet and the at least one test channel; a waste channel communicating with the sampling channel; and a vent opening communicating with the sampling channel. At least the sampling channel and the waste channel each has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic. The sampling channel with its at least one surface portion that is hydrophilic, the vent opening and the waste channel with its at least one surface portion that is hydrophilic, coact to automatically draw a requisite volume of a blood sample deposited at the blood receptor-inlet, into the sampling channel. More specifically, air compressed within the blood clot detection instrument, the at least one test channel of the cuvette, and the section of the sampling channel extending beyond the vent opening of the cuvette, coacts with the waste channel to cause the a leading edge of the blood sample drawn into the sampling channel from the blood receptor-inlet, to pull back within the sampling channel and uncover an optical sensor of the blood clot detection instrument. The volume of the blood sample in the sampling channel at the time when the blood sample is pulled back to uncover the optical sensor, equals the requisite volume. The uncovering of the optical sensor activates a pump module of the blood clot detection instrument, which draws the requisite volume of the blood sample into the at least one test channel.
  • An apparatus is described herein for measuring blood clotting time. The apparatus comprises: a blood clot detection instrument and a cuvette for use with the blood clot detection instrument. The blood clot detection instrument comprises: a pump module and at least one pressure sensor. The cuvette comprises a blood sample receptor-inlet; a channel arrangement comprising: at least one test channel for performing a blood clotting time measurement; a sampling channel communicating with the blood sample receptor-inlet and the at least one test channel; and a waste channel communicating with the sampling channel; and a vent opening communicating with the sampling channel. At least the sampling channel has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic. The sampling channel with its at least one surface portion that is hydrophilic, the vent opening and the waste channel coact to automatically draw a requisite volume of a blood sample deposited at the blood receptor-inlet, into the sampling channel, the requisite volume of blood sample being drawn into the at least one test channel when the pump module of the blood clot detection instrument is activated. The at least one test channel of the cuvette, and the pump module and the at least one pressure sensor of the clot detection instrument, coact to perform a blood clotting time measurement on the requisite volume of the blood sample.
  • Also described herein is a blood clot detection instrument for automatically measuring blood clotting time of a blood sample contained in a test channel of a cuvette. The blood clot detection instrument comprises a pump module for communicating with the test channel of the cuvette; a pressure sensor; and a central processing unit. The central processing unit executes instructions for operating the pump module in a pressure alternating mode that pumps the blood sample back and forth in a test channel of a cuvette. During clot formation, the viscosity of the blood sample increases and causes a pumping pressure of the pump module to increase over time. The central processing unit executes further instructions for obtaining a baseline pumping pressure from the pressure sensor upon initial operation of the pump module in the pressure alternating mode; obtaining additional pumping pressures over time from the pressure sensor; determining a pumping pressure difference value between each additional pumping pressure and the baseline pumping pressure; comparing each pumping pressure difference value to a predetermined threshold value; and indicating the blood clotting time of the blood sample when the pumping pressure difference value exceeds the predetermined threshold value, the indicated blood clotting time comprising a duration of time extending between the measurement of the additional pumping pressure used for determining the pumping pressure difference value that exceeded the predetermined threshold value and the measurement of the baseline pumping pressure.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a schematic view of an embodiment of a cuvette-based apparatus for measuring blood coagulation or clotting time.
  • FIG. 2A is a schematic plan view of an embodiment of the disposable cuvette.
  • FIG. 2B is a sectional view through line 2B-2B of FIG. 2A.
  • FIG. 2C is a sectional view through line 2C-2C of FIG. 2A.
  • FIG. 3A is an enlarged view of a blood sample testing portion of the disposable cuvette shown in FIG. 2A.
  • FIG. 3B is a section view through line 3B-3B of FIG. 3A.
  • FIG. 4 is an enlarged view of a volumetric blood sampling portion of the disposable cuvette shown in FIG. 2A.
  • FIG. 5 is a pressure profile and clot detection graph.
  • FIG. 6A is a schematic plan view of another embodiment of the disposable cuvette.
  • FIG. 6B is a schematic plan view of a further embodiment of the disposable cuvette.
  • FIG. 7A is a perspective view of a further embodiment of the disposable cuvette.
  • FIG. 7B is an enlarged view of encircled area 7B in FIG. 7A.
  • FIG. 7C is a sectional view through line 7C-7C in FIG. 7B.
  • Like reference numbers and designations in the various drawings indicate like elements.
  • DETAILED DESCRIPTION OF THE INVENTION
  • Referring to FIG. 1, there is shown a schematic view of an embodiment of a cuvette-based apparatus 10 for measuring blood coagulation or clotting time. The apparatus 10 generally comprises a disposable cuvette 100 and a blood clot detection instrument 200. The apparatus 10 may be used for measuring blood coagulation time by depositing a sample of blood (whole blood or plasma) onto a specified location of the disposable cuvette 100 and operatively coupling the disposable cuvette 100 to the clot detection instrument 200. The cuvette 100 automatically selects or fills itself with a requisite volume of the blood sample (to be tested) deposited at the specified location of the cuvette 100. The clot detection instrument 200 facilitates automatic mixing of the blood sample with a clotting reagent within the cuvette 100 and automatically measures the clotting time of the selected volume of the blood sample mixed with the clotting reagent within the disposable cuvette 100, without contacting the blood sample. After completion of the measurement, the cuvette 100 may be uncoupled or removed from the clot detection instrument 200 and disposed of. Because the clot detection instrument 200 does not contact the blood sample, another cuvette 100 may be operatively coupled to the clot detection instrument 200 for measuring another blood sample without sterilization or other cleaning of the clot detection instrument 200.
  • Referring still to FIG. 1, the clot detection instrument 200 comprises a pneumatic pump module 210, a motor 220 for driving the pump module 210, a plurality of tubes 230 extending from the pump module 210 for pneumatically coupling with the cuvette 100, a pressure sensor 240 associated with each tube 230 for measuring the pneumatic pressure within the tube 230, and an optical sensor 250 for optically sensing a sampling channel in the cuvette 100. In one embodiment, the optical sensor 250 comprises, but is not limited, to a LED/photo sensor. The clot detection instrument 200 also comprises, without limitation, a central processing unit 260 (CPU) executing instructions for controlling the operation of the motor 220 and thus the pump module 220 via signals received from the optical sensor 250, and determining clotting time based on the pressures sensed by the pressure sensors 240, a display (not shown) for displaying the measured clotting time or other data related to the measurement, a memory 270 for storing previously performed measurements, and buttons, knobs, and/or switches (not shown) for operating the clot detection instrument 200, controlling the display and/or accessing stored data from the memory 270.
  • Referring now to FIGS. 2A-2C, there is collectively shown a schematic plan view of an embodiment of the disposable cuvette 100. The cuvette 100 comprises a substantially planar main body 110 defining generally planar top and bottom surfaces 111, 112. The cuvette main body 110 is typically made from a rigid, transparent hydrophobic or hydrophilic plastic material, using any suitable forming method, such molding. The plastic hydrophobic materials may include, without limitation polystyrene and polytetrafluoroethylene and the plastic hydrophilic materials may include, without limitation, styrene acrylonitrile, acrylonitrile styrene acrylate. The cuvette main body 110 may also be made from other types of rigid, transparent hydrophobic or hydrophilic materials. The cuvette main body 110 includes an arrangement of open channels formed in its bottom surface 112. The open channels are covered and sealed by a thin, substrate 120 that is non-removably attached to the bottom surface 112 of the cuvette body 110 When the cuvette main body 110 is not made from a hydrophilic material or is made from a hydrophobic material, the channels of the channel arrangement each have at least one surface that is hydrophilic, and/or has a hydrophilic coating, and/or has a hydrophilic insert disposed therein (formed, for example, as a tube or liner, thereby fully or partially lining the channel(s)), that facilitates the automatic filling function of the cuvette 100.
  • In one embodiment, at least a top surface 121 of the thin substrate 120, i.e., the surface in contact with the bottom surface 112 of the cuvette body 110, is hydrophilic or has hydrophilic properties. The hydrophilic properties of the top surface 121 of the substrate 120, facilitates the requisite volumetric selection of the blood sample deposited on the cuvette 100, for coagulation time measurement by the clot detection instrument 200. In other embodiments, requisite volumetric selection of the blood sample is accomplished by forming the cuvette body 110 from a hydrophilic material.
  • The thin substrate 120, in one embodiment, is a transparent film 122 coated on one side with a layer 122 a of clear pressure sensitive hydrophilic adhesive. The layer 122 a of hydrophilic adhesive forms the top surface 121 of the substrate 120 and non-removably attaches the substrate 120 to the bottom surface 112 of the cuvette body 110. The transparent film 122 may comprise, in one embodiment, a transparent polyester material.
  • In an alternative embodiment the transparent film 122 is made from a hydrophilic material. Such a substrate may be attached to the bottom surface 112 of the cuvette body 110 (with the top surface 121 of the substrate 120 mated with the bottom surface 112 of the cuvette body 110) with a layer of adhesive applied to the bottom surface 112 of cuvette body 110. Alternatively, such a substrate may be attached to the bottom surface 112 of the cuvette body 110 using heat sealing methods.
  • Referring still to FIGS. 2A-2C, the channel arrangement formed in the bottom surface of the cuvette body 110 generally comprises a sampling channel 130, one or more test channels 140 and at least one waste channel 150. A first end 131 of the sampling channel 130 communicates with a sample depositing area 160 formed in a first or front end 113 of the cuvette body 110. The sample depositing area 160 in the front end 113 of the cuvette body 110 and the exposed underlying portion of the substrate 120 form a blood sample receptor and inlet 161 (receptor-inlet 161) on which the entire blood sample is deposited. The sampling channel 130 extends longitudinally in the bottom surface of the cuvette body 110, from the receptor-inlet 161, and merges at its second end with the one or more test channels 140 formed in the bottom surface of the cuvette body 110.
  • The channel arrangement shown in FIGS. 2A-2C further includes a jumper channel 170 that branches off from the sampling channel 130 just downstream of the receptor-inlet 161 and fluidly connects the waste channel 150 with the sampling channel 130. The terminal end of the waste channel 150 communicates with a waste channel venting aperture 151 formed transversely through the cuvette body 110, which allows “dead” air displaced from within the waste and jumper channels 150, 170 by incoming blood, to be vented to the external environment. The waste channel venting aperture 151 is open to the external environment at the top surface 111 of the cuvette body 110 and closed by the substrate 120 at the bottom surface of the cuvette body 110.
  • The channel arrangement shown in FIGS. 2A-2C further includes a vent channel 180 that branches off from the sampling channel 130 downstream of the jumper channel 170. The vent channel 180 communicates with a vent opening 181 formed transversely through the cuvette body 110 which allows “dead” air displaced from within the sampling and vent channels 130, 180 by incoming blood to be vented to the external environment. The vent opening 181 is open to the external environment at the top surface 111 of the cuvette body 110 and closed by the substrate 120 at the bottom surface of the cuvette body 110.
  • As shown in FIG. 2C, the sampling channel 130 (and the jumper, waste and vent channels 170, 150, 180) formed in the bottom surface 112 of the cuvette main body 110 has a smooth top T surface and smooth side surfaces S. The bottom surface B of the sampling channel 130 (and the jumper, waste and vent channels 170, 150, 180) is formed by the top surface 121 (e.g., hydrophilic adhesive layer 122 a or the top surface of the hydrophilic film 122) of the substrate 120, which is also smooth.
  • The cuvette main body 110, in some embodiments, is made from a hydrophobic material. In such embodiments, the sampling, vent, jumper, and waste channels 130, 180, 170, and 150, respectively, each includes at least one surface that is hydrophilic, and/or has a hydrophilic coating, and/or has a hydrophilic insert disposed therein, that facilitates the automatic sample sizing function of the cuvette 100.
  • In other embodiments, the cuvette main body 110 is made from a hydrophilic material. The one or more test channels 140 in such embodiments, each includes at least one surface that is hydrophobic, and/or has a hydrophobic coating, and/or has a hydrophobic insert disposed therein, where no automatic filling or sample sizing function is required to be performed by the cuvette 100.
  • The requisite volume of blood sample selected by the cuvette 100 for measurement by the clot detection instrument 200, is obtained from the blood sample deposited on the receptor-inlet 161. The size of this volume is determined by the effective volume of the sampling channel 130. The effective volume of the sampling channel 130 is determined by the width of the sampling channel 130, the height of the sampling channel 130, and length of the sampling channel 130 as measured from point A, which is adjacent to the receptor-inlet 161, to point B, which is adjacent to the vent channel 180. The jumper channel 170, connecting the sampling channel 130 to waste channel 150, delays the filling of the waste channel 150 until the sampling channel 130 is completely filled. The duration of the delay is controlled by an intersection I of the jumper channel 170 and the waste channel 150 and the length and cross-sectional area (CSA) of jumper channel 170 relative to the CSA of the waste channel 150, which insure that blood from the blood sample deposited on the receptor-inlet 161, is drawn into the sampling channel 130 prior to being drawn into the waste channel 150. The delay time is determined by the cross section area and length of the jumper channel 170. The duration of the delay may be increased by lengthening the jumper channel 170, and/or decreasing the cross-sectional area (width and height) of the jumper channel 170 relative to the CSA of the waste channel to increase flow resistant through the jumper channel 170. Thus, during automatic blood sample volume sizing, the intersection I of the jumper channel 170 and the waste channel 150 acts like a resistor. Once a blood sample is applied or deposited in the cuvette's receptor-inlet 161, the blood sample enters the sampling channel 130 and the jumper channel 170 substantially simultaneously. While the blood sample moves forward in the sampling channel 130, it also fills the jumper channel 170, then stops at the intersection I of the jumper channel 170 and the waste channel 150. The sampling channel 130 continues to fill until an equilibrium state is reached. The remaining sample in the receptor-inlet 161 then forces the blood sample into the waste channel 150 from the jumper channel 170. The hydrophilic force of the waste channel 150 picks up and draws off the remaining blood sample in the receptor-inlet 161.
  • In one embodiment where the cuvette comprises three test channels 140, the sampling channel 130 has a width of about 0.055 inches, a height of about 0.014 inches, and a length of about 0.9 inches; the vent channel 180 has a width of about 0.010 inches, a height of about 0.012 inches, and a length of about 0.140 inches; the jumper channel 170 has a width of about 0.010 inches, a height of about 0.012 inches, and a length of about 0.25 inches; and and the waste channel 150 has a width of about 0.066 inches, a height of about 0.014 inches, and length of about 2.24 inches. The three test channels 140 of such a cuvette each has a width of about 0.030 inches and a height of about 0.010 inches. The length of each of the outer two test channels is about 1.69 inches and the inner test channel is about 1.634 inches. The sampling, jumper, waste, and test channel(s) in other embodiments of the cuvette may have other suitable dimensions.
  • FIG. 6A shows an another embodiment of the cuvette, denoted by reference number 300. The cuvette 300 is substantially identical to the cuvette 100 shown in FIG. 2A, except that the vent channel extending between the sampling channel and the vent opening is replaced by a vent opening 381 that directly opens into the sampling channel 130.
  • FIG. 6B shows a further embodiment of the cuvette, denoted by reference number 400. The cuvette 400 is substantially identical to the cuvette 100 shown in FIG. 2A, except that the waste channel 450 communicates directly with the sampling channel 130 thereby omitting the jumper channel. In addition, the waste channel 450 includes one or more restrictions 452 located just after the entrance to the waste channel 450 that function to delay filing of the waste channel 450.
  • FIGS. 7A-7C collectively show a further embodiment of a cuvette, denoted by reference number 500. The cuvette 500 is substantially identical to the cuvette 100 shown in FIG. 2A, except that the one or more open test channels 140 are formed in the top surface 111 of the main body 110 instead of in the bottom surface 112 of the main body 110 where the open sampling, vent, jumper, and waste channels 130, 180, 170, 150 are formed. In addition, the open one or more test channels 140 in the top surface 111 of the cuvette main body 110 are covered and sealed by a thin substrate 530 with hydrophobic properties (e.g., the substrate 530 includes a hydrophobic adhesive coating or is a hydrophobic film) that is non-removably attached to the top surface 111 of the cuvette main body 110, and the open sampling, vent, jumper, and waste channels 130, 180, 170, 150 in the bottom surface 112 of the cuvette main body 110 are covered and sealed by a thin, substrate 520 with hydrophilic properties (e.g., the substrate 520 includes a hydrophilic adhesive coating or is a hydrophilic film) that is non-removably attached to the bottom surface 112 of the cuvette body 110. As can be seen in FIGS. 7B and 7C, the sampling channel 103 and an inlet 540 to the one or more test channels 140 are laterally offset from one another. A connecting channel 550 formed in the top surface 111 of the cuvette main body 110, has a first end 550 a that communicates with a terminal end of the sampling channel 103 and a second end 550 b that communicates with an inlet 540 to the one or more test channels 140. The first end 550 a of the connecting channel 550 is covered and sealed by the hydrophillic substrate 520. The remainder of the connecting channel 550 including the second end 550 b thereof, is covered and sealed by the hydrophobic substrate 530. The connecting channel 550 transfers the volume of the blood sample precisely collected by the sampling channel 130, to the one or more test channels 140.
  • In one embodiment, the one or more test channels 140 comprises a branched array of three test channels 140 in a menorah-shaped configuration 140 m (visible in FIGS. 2A, 3A, 4, 6A and 6B). The menorah-shaped array of test channels 140 m evenly divides the selected volume of blood into three separate blood samples, thereby allowing the cuvette 100 to be used for performing up to three different blood tests. For examples of the blood tests that may be performed in the cuvette, see U.S. Pat. No. 5,534,226, entitled, PORTABLE TEST APPARATUS AND ASSOCIATED METHOD OF PERFORMING A BLOOD COAGULATION TEST, assigned to the International Technidyne Corporation, the assignee herein. The entire disclosure of U.S. Pat. No. 5,534,226 is incorporated herein by reference. The branched array in other embodiments of the cuvette 100 may include two test channels 140 or more than three test channels 140.
  • Referring still to FIGS. 2A, 3A, 4, 6A and 6B, the terminal or marginal terminal end of each test channel 140 communicates with a drive aperture 141 formed through the cuvette body 110. The drive aperture 141 is open to the external environment at the top surface 112 of the cuvette body 110 and closed by the substrate 120 at the bottom surface of the cuvette body 110. When the cuvette 100 is operatively coupled to the clot detection instrument 200, as shown in FIG. 1, the plurality of tubes 230 extending from the pump module 210 sealingly engage the one or more drive apertures 141 of the cuvette body 110, so that the arrangement of channels and the pneumatic pump module 210 of the clot detection instrument 200 form a pneumatic system when the cuvette 100 is operatively coupled to the clot detection instrument 200.
  • Referring now to FIGS. 3A and 3B, each of the test channels 140 formed in the bottom surface of the cuvette body 110 includes end sections 142 a with smooth top, side and bottom walls (the bottom wall of each test channel 140 being formed by the smooth top surface 121 of the substrate 120) similar to the top, side and bottom walls of the sampling, jumper and waste channels 130, 170, and 150, and an intermediate section 142 b where the top wall TT and side walls ST are textured. In one non-limiting embodiment, the texturing may comprise a flat knurl cross-hatch. In other embodiments, the texturing in the intermediate section 142 b of one or more of test channels 140 may only be on the top wall or on one or both of the side walls. The length of the textured section is selected so that the blood sample BLD always remains within this section of the test channel 140 during testing. A dehydrated clot promoting reagent (not shown) for triggering and accelerating blood clotting, is disposed in each test channel 140 where the texturing is located. The reagent in each test channel 140 may be the same or different. Therefore, in one embodiment, reagent A may be in each of the test channels. In another embodiment, reagent A may be in two of the test channels and reagent B may be in one of the test channels. In still another embodiment, reagent A may be in one of the test channels, reagent B may be in one of the test channels and reagent C may be in one of the test channels. When the blood sample is drawn into the test channels 140, the reagent rehydrates and mixes with the blood. The textured wall(s) of each test channel 140 improve reagent deposition thereon during manufacture of the cuvette, and increase clotting measurement sensitivity, as the blood sample is reciprocally moved or oscillated therein when measuring of the clotting time of the blood sample, as will be explained further on. In an alternate embodiment, the textured intermediate section of one or more the test channels 140 may be replaced by a restricted area (not shown) where the test channel 140 is narrowed.
  • The automatic volumetric filling function of the cuvette 100 will now be described in greater detail with reference to FIG. 4. Prior to volumetric filling, the cuvette 100 must be operatively coupled to the clot detection instrument 200 such that the plurality of tubes 230 extending from the pump module 210 of the clot detection instrument 200 sealingly engage the one or more drive apertures 141 of the cuvette body 110, thereby creating a pneumatic system formed by the arrangement of channels of the cuvette 100 and the pneumatic pump module 210 of the clot detection instrument 200, as shown in FIG. 1. The automatic volumetric filling function commences when a blood sample is deposited onto the receptor-inlet 161 of the cuvette 100. The blood sample may be deposited on the receptor-inlet 161 by finger after a fingerstick, a needle, a dropper, a pipette, a capillary tube, or any other suitable depositing device. Since at least a portion of the sampling channel 130 is hydrophilic, a force Fs is generated by the hydrophilicity of this portion, which initially draws the blood sample deposited on the receptor-inlet 161 into the sampling channel 130 until the entire vent channel 180 becomes filled. The dead air in the vent channel 180 and the section of the sampling channel 130 extending between the receptor-inlet 161 and the vent channel 180, is vented through the vent opening 181 of the vent channel 180 as the blood BLD fills this section of the sampling channel 130, and the vent channel 180. The blood drawn into the vent channel 180 seals the vent opening 181. At the same time the jumper channel hydrophilicity force Fj draws blood into the jumper channel. Once the vent channel 180 has been filled, the force Fs continues to draw more blood from the blood sample deposited on the receptor-inlet 161 into the sampling channel 130 such that the blood BLD in the sampling channel 130 overshoots the vent channel 180 and covers the optical sensor 250 of the clot detection instrument 200, which lies under or over section or area 131 of the sampling channel 130. The blood BLD which overshoots the vent channel 180 compresses the dead air volume contained within the section of the sampling channel 130 extending beyond the vent channel 180, the test channels 140, and the tubes 230 of the clot detection instrument 200, and the pump module 210, because Fs>Fp and Fw<<Fs, where Fp is the pressure of the compressed dead air volume, and Fw is the hydrophilicity force generated by at least a portion of the waste channel 150 that is hydrophilic. Blood stops flowing in the sampling channel 130 towards the test channels 140 when an equilibrium state Fs=Fp+Fw is achieved therein.
  • After the equilibrium state has been reached, blood that has been delayed by the the jumper channel/waste channel intersection I and the jumper channel 170, reaches the waste channel 150. The waste channel 150 generates a force Fw, that increases to a value proportional to the line of contact between the blood and the hydrophilic surface, which first pulls additional blood remaining in the receptor-inlet 161 into the waste channel 150. As the waste channel 150 fills with excess blood sample BLD, dead air disposed therein and displaced by the incoming blood BLD is vented to the external environment through the waste channel venting aperture 151. Once the remaining blood sample drawn off from the receptor-inlet 161, force Fw+Fp becomes greater than Fs, and therefore, the leading edge E of the blood BLD in the sampling channel 130 starts pulling back towards the vent channel 180.
  • The leading edge E of the blood BLD in the sampling channel 130 continues to be pulled back by force Fw+Fp and uncovers the optical sensor 250. The volume of the blood sample BLD disposed in the sampling channel 130 at the moment the optical sensor 250 is uncovered, is the requisite volume. Consequently, the pump module 210 of the clot detection instrument 200 is immediately activated by the uncovered optical sensor 250 and draws this requisite volume of blood sample BLD into the test channels 140 such that the blood sample BLD is disposed in the sections of the test channels 140 that are textured. The ratio of force Fw to force Fs determines the sample pull back speed. Generally, a wider waste channel 150 has stronger pull back. In one, non-limiting embodiment, the ratio of force Fw to force Fs equals 1.2. One of ordinary skill in the art will recognize that the forces described above may be adjusted by the material properties of the cuvette body 110, substrate 120, size and/or geometry of the plurality of channels. The blood sample over shoot and pull back functions of the sampling channel 130 may also be adjusted and controlled by the volume of dead air in the tubes 230 and pump module 210 of the clot detection instrument 200.
  • The automatic blood clot testing function of the cuvette 100 will now be described in greater detail with reference to FIGS. 3A and 5. After the pump module 210 has drawn the blood sample into one or more test channels 140 of the cuvette 100, the pump module 210 automatically switches into a pumping mode where it alternately creates positive and negative pressures in the test channels 140 of the cuvette 100. The alternating positive and negative pressures (pumping pressure) reciprocally moves the blood samples BLD back and forth across textured sections (or restricted areas) of the one or more test channels 140, thereby mixing the blood sample with dehydrated reagent, as shown in FIG. 3A. As the reagent rehydrates and mixes with the blood sample BLD, it triggers and accelerates the blood clotting cascade. Fibrin formation within the blood sample BLD causes the viscosity of the blood sample BLD to increase with time. The viscosity increase may be detected, in one embodiment, by measuring the pumping pressure within each test channel 140 over time. As shown in the graph of FIG. 5, the pumping pressure starts at an initial pumping pressure value (pumping pressure baseline ΔPbaseline) and increases with time, as the viscosity of the blood increases during clotting. The pressure sensors 240 of the blood clot detection instrument 200, measure the pump pressure over time and the CPU 260 of the clot detection instrument 200 compares this data to the initial pressure baseline ΔPbaseline. The clotting time of the blood sample may be determined when pressure value is greater than or equal to a preset threshold. In one embodiment, the clotting time is,

  • ΔP end point −ΔP baseline≧threshold,
  • where ΔPend point is the clotting end point peak to peak pressure.
  • The preset threshold may be fixed or dynamic. In one embodiment, a dynamic threshold may be,

  • ΔP baseline+(0.3×ΔP baseline).
  • In general, the hydrophilicity of the one or more test channels 140 will aid the robust automatic volumetric blood sample filling function of the cuvette 100, while impeding the clotting performance of the cuvette 100. Appropriately balancing the test channel 140 dimensions, geometry, degree of texturing/restriction size, and the hydrophilic properties of the cuvette body 110 and substrate 120, will provide the cuvette 100 with requisite blood clotting performance.
  • The pump profile of the pump module 210, i.e., pumping speed and stroke, may also affect clotting performance. For example, a pump speed greater than 20 millisecond (ms) per pump step, equivalent to 20 ul per sec in test channel or a pump stroke greater than 55 steps, equivalent to 0.044, may increase the chance of deforming a weak clot (International Normalized Ratio>4.0), which may in turn, result in lower clot detection precision. In one embodiment, the pump profile is 40 ms per pump step and 36 steps per pump direction (generates positive and negative pressures).
  • While exemplary drawings and specific embodiments have been described and illustrated, it is to be understood that that the scope of the present invention is not to be limited to the particular embodiments discussed. Thus, the embodiments shall be regarded as illustrative rather than restrictive, and it should be understood that variations may be made in those embodiments by workers skilled in the art without departing from the scope of the present invention as set forth in the claims that follow and their structural and functional equivalents.

Claims (57)

1. A cuvette for use with a blood clot detection instrument, the cuvette comprising:
a main body including:
a blood sample receptor-inlet;
a channel arrangement comprising:
at least one test channel for performing a blood clotting time measurement;
a sampling channel communicating with the blood sample receptor-inlet and the at least one test channel, at least the sampling channel having at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic; and
a waste channel communicating with the sampling channel; and
a vent opening communicating with the sampling channel,
wherein the sampling channel, the vent opening and the waste channel coact to automatically draw a requisite volume of a blood sample deposited at the blood receptor-inlet, into the sampling channel.
2. The cuvette of claim 1, wherein the coaction between the sampling channel and the vent opening includes a force generated by the at least one surface portion of the sampling channel that is hydrophilic and which draws the blood from the blood sample deposited at the blood sample receptor-inlet into the sampling channel and venting of air through the vent opening which is displaced from the sampling channel by the incoming blood.
3. The cuvette of claim 1, wherein the channel arrangement further comprises a vent channel connecting the vent opening with the sampling channel.
4. The cuvette of claim 1, wherein the channel arrangement further comprises a member associated with the waste channel for delaying the filling of the waste channel until the sampling channel is filled.
5. The cuvette of claim 1, wherein the channel arrangement is formed in a surface of the main body.
6. The cuvette of claim 5, further comprising a substrate for closing and sealing at least a portion of the channel arrangement formed in the surface of the main body.
7. The cuvette of claim 6, wherein the substrate forms the at least one surface portion of the sampling channel that is hydrophilic.
8. The cuvette of claim 6, wherein the substrate comprises a film with a hydrophilic surface, the hydrophilic surface of the substrate forming the at least one surface portion of the sampling channel that is hydrophilic.
9. The cuvette of claim 6, wherein the substrate comprises a film and a layer of hydrophilic material disposed on the film, the hydrophilic material forming the at least one surface portion of the sampling channel that is hydrophilic.
10. The cuvette of claim 9, wherein the hydrophilic material is an adhesive which attaches the substrate to the main body.
11. The cuvette of claim 1, further comprising a blood clotting reagent disposed in the at least one test channel.
12. The cuvette of claim 1, wherein the at least one test channel includes a section having at least one textured surface.
13. The cuvette of claim 1, wherein the at least one test channel includes a restriction.
14. The cuvette of claim 1, wherein the main body is made of one of a hydrophobic material, a hydrophilic material, or a combination of a hydrophobic material and a hydrophilic material.
15. The cuvette of claim 1, wherein the waste channel has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic.
16. The cuvette of claim 1, wherein the at least one test channel has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic or hydrophobic.
17. The cuvette of claim 3, wherein the vent channel has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic.
18. The cuvette of claim 4, wherein the member associated with the waste channel comprises a jumper channel or a restriction.
19. The cuvette of claim 18, wherein the jumper channel or the restriction has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic.
20. The cuvette of claim 1, wherein the channel arrangement further comprises a jumper channel connecting the waste channel with the sampling channel, the jumper channel for delaying the filling of the waste channel until the sampling channel is filled.
21. An apparatus for measuring blood clotting time, the apparatus comprising:
A) a blood clot detection instrument, the blood clot detection instrument comprising:
a pump module; and
at least one pressure sensor; and
B) a cuvette for use with the blood clot detection instrument, the cuvette comprising:
a main body including:
i) a blood sample receptor-inlet;
ii) a channel arrangement comprising:
a) at least one test channel for communicating with the pump module when the cuvette is operatively coupled to the clot detection instrument;
b) a sampling channel communicating with the blood sample receptor-inlet and the at least one test channel, at least the sampling channel having at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic; and
c) a waste channel communicating with the sampling channel;
 and
iii) a vent opening communicating with the sampling channel,
wherein compressed air within the blood clot detection instrument and the at least one test channel, the sampling channel, the vent opening and waste channel, coact to automatically draw a requisite volume of a blood sample deposited at the blood receptor-inlet, into the sampling channel, and
wherein the at least one test channel of the cuvette, and the pump module and the at least one pressure sensor of the clot detection instrument, coact to perform a blood clotting time measurement on the requisite volume of the blood sample.
22. The apparatus of claim 21, wherein the coaction between the sampling channel and the vent opening includes a force generated by the at least one surface portion of the sampling channel that is hydrophilic and which draws the blood from the blood sample deposited at the blood sample receptor-inlet into the sampling channel and venting of air through the vent opening which is displaced from the sampling channel by the incoming blood.
23. The apparatus of claim 21, wherein the channel arrangement further comprises a vent channel connecting the vent opening with the sampling channel.
24. The apparatus of claim 21, wherein the channel arrangement further comprises a member associated with the waste channel for delaying the filling of the waste channel until the sampling channel is filled.
25. The apparatus of claim 21, wherein the channel arrangement is formed in a surface of the main body.
26. The apparatus of claim 25, further comprising a substrate for closing and sealing at least a portion of the channel arrangement formed in the surface of the main body.
27. The apparatus of claim 26, wherein the substrate forms the at least one surface portion of the sampling channel that is hydrophilic.
28. The apparatus of claim 26, wherein the substrate comprises a film with a hydrophilic surface, the hydrophilic surface of the substrate forming the at least one surface portion of the sampling channel that is hydrophilic.
29. The apparatus of claim 26, wherein the substrate comprises a film and a layer of hydrophilic material disposed on the film, the hydrophilic material forming the at least one surface portion of the sampling channel that is hydrophilic.
30. The apparatus of claim 29, wherein the hydrophilic material is an adhesive which attaches the substrate to the main body.
31. The apparatus of claim 21, further comprising a blood clotting reagent disposed in the at least one test channel.
32. The apparatus of claim 21, wherein the at least one test channel includes a section having at least one textured surface.
33. The apparatus of claim 21, wherein the at least one test channel includes a restriction.
34. The apparatus of claim 21, wherein the main body is made of one of a hydrophobic material, a hydrophilic material, or a combination of a hydrophobic material and a hydrophilic material.
35. The apparatus of claim 21, wherein the waste channel has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic.
36. The apparatus of claim 21, wherein the at least one test channel has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic or hydrophobic.
37. The apparatus of claim 23, wherein the vent channel has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic.
38. The apparatus of claim 24, wherein the member associated with the waste channel comprises a jumper channel or a restriction.
39. The apparatus of claim 38, wherein the jumper channel or restriction has at least one surface portion, a coating, an insert or liner, and any combination thereof, that is hydrophilic.
40. The apparatus of claim 21, wherein the channel arrangement further comprises a jumper channel connecting the waste channel with the sampling channel, the jumper channel for delaying the filling of the waste channel until the sampling channel is filled.
41. A blood clot detection instrument for automatically measuring blood clotting time of a blood sample contained in a test channel of a cuvette, the blood clot detection instrument comprising:
a pump module for communicating with the test channel of the cuvette;
a pressure sensor; and
a central processing unit executing instructions for:
operating the pump module in a pressure alternating mode that causes a viscosity of the blood sample to increase over time, the increase in viscosity of the blood causing a pumping pressure of the pump module to increase over time;
obtaining a baseline pumping pressure from the pressure sensor upon initial operation of the pump module in the pressure alternating mode;
obtaining additional pumping pressures over time from the pressure sensor;
determining a pumping pressure difference value between each additional pumping pressure and the baseline pumping pressure;
comparing the pumping pressure difference value to a predetermined threshold value; and
indicating the blood clotting time of the blood sample when the pumping pressure difference value equals or exceeds the predetermined threshold value,
the indicated blood clotting time comprising a duration of time extending between the measurement of the additional pumping pressure used for determining the pumping pressure difference value that exceeded the predetermined threshold value and the measurement of the baseline pumping pressure.
42. The blood clot detection instrument of claim 41, wherein the predetermined threshold may be fixed or dynamic.
43. The blood clot detection instrument of claim 41, wherein the pump module, in the pressure alternating mode, creates positive and negative pressures in the test channel of the cuvette.
44. The blood clot detection instrument of claim 41, wherein the pump module, in the pressure alternating mode, reciprocally moves the blood sample back and forth across a textured section or restricted area of the test channel, thereby mixing the blood sample with a reagent disposed in the test channel that triggers and accelerates clotting of the blood sample.
45. The cuvette of claim 1, wherein the at least one test channel comprises three test channels and further comprising a reagent in each of the test channels.
46. The cuvette of claim 45, wherein the reagents are all the same, different, or combinations thereof.
47. The apparatus of claim 21, wherein the at least one test channel comprises three test channels and further comprising a reagent in each of the test channels.
48. The apparatus of claim 47, wherein the reagents are all the same, different, or combinations thereof.
49. The apparatus of claim 21, wherein air compressed within the blood clot detection instrument, the at least one test channel of the cuvette, and the section of the sampling channel extending beyond the vent opening of the cuvette, coacts with the waste channel to cause a leading edge of the blood sample drawn into the sampling channel from the blood receptor-inlet, to pull back within the sampling channel and uncover an optical sensor of the blood clot detection instrument, the volume of the blood sample in the sampling channel at the time when the blood sample is pulled back to uncover the optical sensor, equaling the requisite volume, the uncovering of the optical sensor activating the pump module of the blood clot detection instrument, which draws the requisite volume of the blood sample into the at least one test channel.
50. The cuvette of claim 1, further comprising:
a first substrate with hydrophilic properties for closing and sealing the sampling channel and the waste channel; and
a second substrate with hydrophobic properties for closing and sealing the at least one test channel.
51. The cuvette of claim 50, wherein the sampling channel and the waste channel are formed in a first surface of the cuvette and the first substrate is affixed to the first surface, and the at least one test channel is formed in second surface of the cuvette and the second substrate is affixed to the second surface.
52. The cuvette of claim 51, wherein the first and second surfaces are opposed to one another.
53. The cuvette of claim 50, wherein the channel arrangement further comprises:
a vent channel connecting the vent opening with sampling channel; and
a jumper channel connecting the waste channel to the sampling channel, for delaying the filling of the waste channel until the sampling channel is filled,
wherein the first substrate closes and seals the vent channel and the jumper channel.
54. The apparatus of claim 21, further comprising;
a first substrate with hydrophilic properties for closing and sealing the sampling channel and the waste channel; and
a second substrate with hydrophobic properties for closing and sealing the at least one test channel.
55. The apparatus of claim 54, wherein the sampling channel and the waste channel are formed in a first surface of the cuvette and the first substrate is affixed to the first surface, and the at least one test channel is formed in second surface of the cuvette and the second substrate is affixed to the second surface.
56. The apparatus of claim 55, wherein the first and second surfaces are opposed to one another.
57. The apparatus of claim 54, wherein the channel arrangement further comprises:
a vent channel connecting the vent opening with sampling channel; and
a jumper channel connecting the waste channel to the sampling channel, for delaying the filling of the waste channel until the sampling channel is filled,
wherein the first substrate closes and seals the vent channel and the jumper channel.
US12/503,665 2008-07-16 2009-07-15 Cuvette-based apparatus for blood coagulation measurement and testing Abandoned US20100028207A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US12/503,665 US20100028207A1 (en) 2008-07-16 2009-07-15 Cuvette-based apparatus for blood coagulation measurement and testing
US13/474,243 US20130017126A1 (en) 2008-07-16 2012-05-17 Cuvette-Based Apparatus for Blood Coagulation Measurement and Testing
US13/959,007 US10180419B2 (en) 2008-07-16 2013-08-05 Cuvette-based apparatus for blood coagulation measurement and testing
US16/210,433 US10578605B2 (en) 2008-07-16 2018-12-05 Cuvette-based apparatus for blood coagulation measurement and testing
US16/805,375 US11402369B2 (en) 2008-07-16 2020-02-28 Cuvette-based apparatus for blood coagulation measurement and testing

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US8129008P 2008-07-16 2008-07-16
US12/503,665 US20100028207A1 (en) 2008-07-16 2009-07-15 Cuvette-based apparatus for blood coagulation measurement and testing

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US13/474,243 Continuation US20130017126A1 (en) 2008-07-16 2012-05-17 Cuvette-Based Apparatus for Blood Coagulation Measurement and Testing

Publications (1)

Publication Number Publication Date
US20100028207A1 true US20100028207A1 (en) 2010-02-04

Family

ID=41550706

Family Applications (5)

Application Number Title Priority Date Filing Date
US12/503,665 Abandoned US20100028207A1 (en) 2008-07-16 2009-07-15 Cuvette-based apparatus for blood coagulation measurement and testing
US13/474,243 Abandoned US20130017126A1 (en) 2008-07-16 2012-05-17 Cuvette-Based Apparatus for Blood Coagulation Measurement and Testing
US13/959,007 Active 2031-07-02 US10180419B2 (en) 2008-07-16 2013-08-05 Cuvette-based apparatus for blood coagulation measurement and testing
US16/210,433 Active US10578605B2 (en) 2008-07-16 2018-12-05 Cuvette-based apparatus for blood coagulation measurement and testing
US16/805,375 Active 2030-04-15 US11402369B2 (en) 2008-07-16 2020-02-28 Cuvette-based apparatus for blood coagulation measurement and testing

Family Applications After (4)

Application Number Title Priority Date Filing Date
US13/474,243 Abandoned US20130017126A1 (en) 2008-07-16 2012-05-17 Cuvette-Based Apparatus for Blood Coagulation Measurement and Testing
US13/959,007 Active 2031-07-02 US10180419B2 (en) 2008-07-16 2013-08-05 Cuvette-based apparatus for blood coagulation measurement and testing
US16/210,433 Active US10578605B2 (en) 2008-07-16 2018-12-05 Cuvette-based apparatus for blood coagulation measurement and testing
US16/805,375 Active 2030-04-15 US11402369B2 (en) 2008-07-16 2020-02-28 Cuvette-based apparatus for blood coagulation measurement and testing

Country Status (6)

Country Link
US (5) US20100028207A1 (en)
EP (1) EP2313767B1 (en)
JP (1) JP2011528439A (en)
CN (1) CN102099676B (en)
ES (1) ES2451541T3 (en)
WO (1) WO2010009267A1 (en)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120046883A1 (en) * 2009-04-27 2012-02-23 El Spectra Llc Pipette instrument
US20140038299A1 (en) * 2007-09-20 2014-02-06 Iline Microsystems, S.L. Microfluidic device and method for fluid clotting time determination
US20140309553A1 (en) * 2013-04-11 2014-10-16 Rarecyte, Inc. Kits and methods for separating a target analyte from a suspension
US9180449B2 (en) 2012-06-12 2015-11-10 Hach Company Mobile water analysis
US9182353B2 (en) 2010-07-22 2015-11-10 Hach Company Lab-on-a-chip for alkalinity analysis
US20160045883A1 (en) * 2013-05-07 2016-02-18 Gencell Biosystems Ltd. Stabilisation features
USD768872S1 (en) 2012-12-12 2016-10-11 Hach Company Cuvette for a water analysis instrument
US20160334403A1 (en) * 2011-01-21 2016-11-17 Theranos, Inc. Systems and methods for sample use maximization
US9952240B2 (en) 2011-09-25 2018-04-24 Theranos Ip Company, Llc Systems and methods for multi-analysis
US10012664B2 (en) 2011-09-25 2018-07-03 Theranos Ip Company, Llc Systems and methods for fluid and component handling
US10518265B2 (en) 2011-09-25 2019-12-31 Theranos Ip Company, Llc Systems and methods for fluid handling
US10634667B2 (en) 2007-10-02 2020-04-28 Theranos Ip Company, Llc Modular point-of-care devices, systems, and uses thereof
US10976330B2 (en) 2011-09-25 2021-04-13 Labrador Diagnostics Llc Fluid handling apparatus and configurations
US11035780B2 (en) 2016-12-22 2021-06-15 Lintec Corporation Cover film for testing, testing member, and method of manufacturing cover film for testing
US11054432B2 (en) 2011-09-25 2021-07-06 Labrador Diagnostics Llc Systems and methods for multi-purpose analysis
US11162936B2 (en) 2011-09-13 2021-11-02 Labrador Diagnostics Llc Systems and methods for multi-analysis
IT202100021401A1 (en) * 2021-08-20 2023-02-20 Giuseppe Piccinni IgG/IgM serological rapid test

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010009267A1 (en) 2008-07-16 2010-01-21 International Technidyne Corporation Cuvette-based apparatus for blood coagulation measurement and testing
KR101193566B1 (en) 2011-08-10 2012-10-22 고려대학교 산학협력단 Apparatus of platelet multi-function analysis based on micro-chip
CN103383391B (en) * 2012-05-04 2015-07-08 北京尚位非凡医药科技有限公司 Detection apparatus for blood clotting time
CN103063612B (en) * 2012-12-28 2015-03-18 深圳市锦瑞电子有限公司 Measurement and analysis method for coagulation analyzer, and coagulation analyzer
KR101497193B1 (en) * 2012-12-31 2015-03-03 고려대학교 산학협력단 Apparatus and method for monitoring platelet function and drug response using centrifugation-based microfluidics
CN104597228B (en) * 2015-01-20 2016-06-15 重庆科技学院 A kind of cell flow morphologic observation chip and using method
CN107074526B (en) * 2015-01-30 2019-06-04 惠普发展公司,有限责任合伙企业 Micro-fluid chip for blood coagulation sensing
CN108627636B (en) * 2017-03-23 2022-03-01 北京碧澄生物科技有限公司 Device and method for detecting liquid solidification
CN110573882B (en) * 2018-01-16 2021-06-25 株式会社爱蓓儿 Cartridge for measuring blood coagulation time and blood coagulation time measuring device
CN108872477B (en) * 2018-03-20 2020-12-08 迈克医疗电子有限公司 Clot detection method and device, terminal device and medium
CN108614306B (en) * 2018-03-20 2020-03-27 迈克医疗电子有限公司 Clot detection method and device, terminal device and medium
CN108872475A (en) * 2018-03-20 2018-11-23 迈克医疗电子有限公司 A kind of method, apparatus of clot detection, terminal device and medium
JP7216365B2 (en) * 2018-10-01 2023-02-01 旭化成株式会社 Photosensitive resin laminate for microchannel
CA3134917A1 (en) * 2019-03-26 2020-10-01 Siemens Healthcare Diagnostics Inc. System for delivering fluid samples through a fluidic device and methods therefor
TWI765205B (en) * 2019-12-31 2022-05-21 台灣嘉碩科技股份有限公司 Planar apparatus for volumetric body fluid collection and manufacturing method thereof

Citations (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4497774A (en) * 1981-06-19 1985-02-05 Medical Laboratory Automation, Inc. Coagulation instrument for performing clotting tests
US5154082A (en) * 1991-05-20 1992-10-13 International Technidyne Corporation Microprocessor-controlled apparatus and method for detecting the coagulation of blood
US5164598A (en) * 1985-08-05 1992-11-17 Biotrack Capillary flow device
US5181415A (en) * 1990-07-20 1993-01-26 Serbio Apparatus for detecting a change of viscosity by measuring a relative slip, in particular for detecting the coagulation rate of blood
US5230866A (en) * 1991-03-01 1993-07-27 Biotrack, Inc. Capillary stop-flow junction having improved stability against accidental fluid flow
US5236666A (en) * 1989-12-01 1993-08-17 Akzo N.V. Temperature regulation in a sample handling system for an optical monitoring system
US5258719A (en) * 1991-06-07 1993-11-02 Sumitomo Chemical Co., Ltd. Capacitive coagulation detecting device for mixed phase container
US5272912A (en) * 1992-03-30 1993-12-28 Yayoi Co., Ltd. Apparatus and method for measuring viscosities of liquids
US5302348A (en) * 1992-12-10 1994-04-12 Itc Corporation Blood coagulation time test apparatus and method
US5478751A (en) * 1993-12-29 1995-12-26 Abbott Laboratories Self-venting immunodiagnositic devices and methods of performing assays
US5591403A (en) * 1994-10-21 1997-01-07 International Technidyne Corporation Portable prothrombin time test apparatus and associated method of performing a prothrombin time test
US5628961A (en) * 1993-10-28 1997-05-13 I-Stat Corporation Apparatus for assaying viscosity changes in fluid samples and method of conducting same
US5646046A (en) * 1989-12-01 1997-07-08 Akzo Nobel N.V. Method and instrument for automatically performing analysis relating to thrombosis and hemostasis
US5836360A (en) * 1997-03-25 1998-11-17 International Technidyne Corporation Volume controlled receptacle
US6084660A (en) * 1998-07-20 2000-07-04 Lifescan, Inc. Initiation of an analytical measurement in blood
US20020123134A1 (en) * 2000-12-26 2002-09-05 Mingxian Huang Active and biocompatible platforms prepared by polymerization of surface coating films
US6451610B1 (en) * 1999-04-14 2002-09-17 International Technidyne Corporation Method and apparatus for coagulation based assays
US6575017B1 (en) * 1993-08-31 2003-06-10 Roche Diagnostics Corporation, Inc. Fluid dose, flow and coagulation sensor for medical instrument
US6750053B1 (en) * 1999-11-15 2004-06-15 I-Stat Corporation Apparatus and method for assaying coagulation in fluid samples
US6915919B2 (en) * 2002-11-21 2005-07-12 American Bio Medica Corporation Container closure cap with self-sealing slot
US6955923B2 (en) * 2001-08-24 2005-10-18 Roche Diagnostics Operations, Inc. Device and method for investigating the flowability of a physiological fluid sample
US7005857B2 (en) * 2000-12-19 2006-02-28 Lifescan Scotland Limited Device for measuring blood coagulation and method thereof
US7059352B2 (en) * 2004-03-31 2006-06-13 Lifescan Scotland Triggerable passive valve for use in controlling the flow of fluid
US7156117B2 (en) * 2004-03-31 2007-01-02 Lifescan Scotland Limited Method of controlling the movement of fluid through a microfluidic circuit using an array of triggerable passive valves
US7497997B2 (en) * 2002-12-26 2009-03-03 Meso Scale Technologies, Llc Assay cartridges and methods of using the same

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5736404A (en) * 1995-12-27 1998-04-07 Zia Yassinzadeh Flow detection appartus and method
US6521182B1 (en) * 1998-07-20 2003-02-18 Lifescan, Inc. Fluidic device for medical diagnostics
DE10305050A1 (en) 2003-02-07 2004-08-19 Roche Diagnostics Gmbh Analytical test element and method for blood tests
EP1619994A4 (en) 2003-04-16 2009-03-11 Univ Drexel Acoustic blood analyzer for assessing blood properties
US7439069B2 (en) 2004-02-27 2008-10-21 Nippoldt Douglas D Blood coagulation test cartridge, system, and method
WO2010009267A1 (en) 2008-07-16 2010-01-21 International Technidyne Corporation Cuvette-based apparatus for blood coagulation measurement and testing

Patent Citations (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4497774A (en) * 1981-06-19 1985-02-05 Medical Laboratory Automation, Inc. Coagulation instrument for performing clotting tests
US5164598A (en) * 1985-08-05 1992-11-17 Biotrack Capillary flow device
US5646046A (en) * 1989-12-01 1997-07-08 Akzo Nobel N.V. Method and instrument for automatically performing analysis relating to thrombosis and hemostasis
US5236666A (en) * 1989-12-01 1993-08-17 Akzo N.V. Temperature regulation in a sample handling system for an optical monitoring system
US5181415A (en) * 1990-07-20 1993-01-26 Serbio Apparatus for detecting a change of viscosity by measuring a relative slip, in particular for detecting the coagulation rate of blood
US5230866A (en) * 1991-03-01 1993-07-27 Biotrack, Inc. Capillary stop-flow junction having improved stability against accidental fluid flow
US5154082A (en) * 1991-05-20 1992-10-13 International Technidyne Corporation Microprocessor-controlled apparatus and method for detecting the coagulation of blood
US5258719A (en) * 1991-06-07 1993-11-02 Sumitomo Chemical Co., Ltd. Capacitive coagulation detecting device for mixed phase container
US5272912A (en) * 1992-03-30 1993-12-28 Yayoi Co., Ltd. Apparatus and method for measuring viscosities of liquids
US5302348A (en) * 1992-12-10 1994-04-12 Itc Corporation Blood coagulation time test apparatus and method
US6575017B1 (en) * 1993-08-31 2003-06-10 Roche Diagnostics Corporation, Inc. Fluid dose, flow and coagulation sensor for medical instrument
US5628961A (en) * 1993-10-28 1997-05-13 I-Stat Corporation Apparatus for assaying viscosity changes in fluid samples and method of conducting same
US5478751A (en) * 1993-12-29 1995-12-26 Abbott Laboratories Self-venting immunodiagnositic devices and methods of performing assays
US5591403A (en) * 1994-10-21 1997-01-07 International Technidyne Corporation Portable prothrombin time test apparatus and associated method of performing a prothrombin time test
US5800781A (en) * 1994-10-21 1998-09-01 International Technidyne Corporation Blood sampling device
US5836360A (en) * 1997-03-25 1998-11-17 International Technidyne Corporation Volume controlled receptacle
US6084660A (en) * 1998-07-20 2000-07-04 Lifescan, Inc. Initiation of an analytical measurement in blood
US6451610B1 (en) * 1999-04-14 2002-09-17 International Technidyne Corporation Method and apparatus for coagulation based assays
US6750053B1 (en) * 1999-11-15 2004-06-15 I-Stat Corporation Apparatus and method for assaying coagulation in fluid samples
US7005857B2 (en) * 2000-12-19 2006-02-28 Lifescan Scotland Limited Device for measuring blood coagulation and method thereof
US20020123134A1 (en) * 2000-12-26 2002-09-05 Mingxian Huang Active and biocompatible platforms prepared by polymerization of surface coating films
US6955923B2 (en) * 2001-08-24 2005-10-18 Roche Diagnostics Operations, Inc. Device and method for investigating the flowability of a physiological fluid sample
US6915919B2 (en) * 2002-11-21 2005-07-12 American Bio Medica Corporation Container closure cap with self-sealing slot
US7497997B2 (en) * 2002-12-26 2009-03-03 Meso Scale Technologies, Llc Assay cartridges and methods of using the same
US7059352B2 (en) * 2004-03-31 2006-06-13 Lifescan Scotland Triggerable passive valve for use in controlling the flow of fluid
US7156117B2 (en) * 2004-03-31 2007-01-02 Lifescan Scotland Limited Method of controlling the movement of fluid through a microfluidic circuit using an array of triggerable passive valves

Cited By (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140038299A1 (en) * 2007-09-20 2014-02-06 Iline Microsystems, S.L. Microfluidic device and method for fluid clotting time determination
US9213036B2 (en) * 2007-09-20 2015-12-15 Iline Microsystems, S.L. Method for fluid clotting time determination on a microfluidic device
US11199538B2 (en) 2007-10-02 2021-12-14 Labrador Diagnostics Llc Modular point-of-care devices, systems, and uses thereof
US11143647B2 (en) 2007-10-02 2021-10-12 Labrador Diagnostics, LLC Modular point-of-care devices, systems, and uses thereof
US11137391B2 (en) 2007-10-02 2021-10-05 Labrador Diagnostics Llc Modular point-of-care devices, systems, and uses thereof
US10634667B2 (en) 2007-10-02 2020-04-28 Theranos Ip Company, Llc Modular point-of-care devices, systems, and uses thereof
US9470616B2 (en) * 2009-04-27 2016-10-18 E.I. Spectra, Llc Pipette instrument
US20120046883A1 (en) * 2009-04-27 2012-02-23 El Spectra Llc Pipette instrument
US9182353B2 (en) 2010-07-22 2015-11-10 Hach Company Lab-on-a-chip for alkalinity analysis
US10557786B2 (en) * 2011-01-21 2020-02-11 Theranos Ip Company, Llc Systems and methods for sample use maximization
US20160334403A1 (en) * 2011-01-21 2016-11-17 Theranos, Inc. Systems and methods for sample use maximization
US11162936B2 (en) 2011-09-13 2021-11-02 Labrador Diagnostics Llc Systems and methods for multi-analysis
US10976330B2 (en) 2011-09-25 2021-04-13 Labrador Diagnostics Llc Fluid handling apparatus and configurations
US9952240B2 (en) 2011-09-25 2018-04-24 Theranos Ip Company, Llc Systems and methods for multi-analysis
US10371710B2 (en) 2011-09-25 2019-08-06 Theranos Ip Company, Llc Systems and methods for fluid and component handling
US10518265B2 (en) 2011-09-25 2019-12-31 Theranos Ip Company, Llc Systems and methods for fluid handling
US10534009B2 (en) 2011-09-25 2020-01-14 Theranos Ip Company, Llc Systems and methods for multi-analysis
US10557863B2 (en) 2011-09-25 2020-02-11 Theranos Ip Company, Llc Systems and methods for multi-analysis
US10018643B2 (en) 2011-09-25 2018-07-10 Theranos Ip Company, Llc Systems and methods for multi-analysis
US10627418B2 (en) 2011-09-25 2020-04-21 Theranos Ip Company, Llc Systems and methods for multi-analysis
US10012664B2 (en) 2011-09-25 2018-07-03 Theranos Ip Company, Llc Systems and methods for fluid and component handling
US11524299B2 (en) 2011-09-25 2022-12-13 Labrador Diagnostics Llc Systems and methods for fluid handling
US11009516B2 (en) 2011-09-25 2021-05-18 Labrador Diagnostics Llc Systems and methods for multi-analysis
US11054432B2 (en) 2011-09-25 2021-07-06 Labrador Diagnostics Llc Systems and methods for multi-purpose analysis
US9180449B2 (en) 2012-06-12 2015-11-10 Hach Company Mobile water analysis
USD768872S1 (en) 2012-12-12 2016-10-11 Hach Company Cuvette for a water analysis instrument
US20140309553A1 (en) * 2013-04-11 2014-10-16 Rarecyte, Inc. Kits and methods for separating a target analyte from a suspension
US20160045883A1 (en) * 2013-05-07 2016-02-18 Gencell Biosystems Ltd. Stabilisation features
US10143989B2 (en) * 2013-05-07 2018-12-04 Gencell Biosystems Ltd. Stabilisation features
US11035780B2 (en) 2016-12-22 2021-06-15 Lintec Corporation Cover film for testing, testing member, and method of manufacturing cover film for testing
IT202100021401A1 (en) * 2021-08-20 2023-02-20 Giuseppe Piccinni IgG/IgM serological rapid test

Also Published As

Publication number Publication date
US10180419B2 (en) 2019-01-15
CN102099676B (en) 2016-01-20
EP2313767A4 (en) 2012-08-08
ES2451541T3 (en) 2014-03-27
WO2010009267A8 (en) 2011-02-03
US11402369B2 (en) 2022-08-02
US20190107529A1 (en) 2019-04-11
WO2010009267A1 (en) 2010-01-21
CN102099676A (en) 2011-06-15
US20130017126A1 (en) 2013-01-17
US20200200731A1 (en) 2020-06-25
US20140161668A1 (en) 2014-06-12
EP2313767A1 (en) 2011-04-27
US10578605B2 (en) 2020-03-03
EP2313767B1 (en) 2014-02-26
JP2011528439A (en) 2011-11-17

Similar Documents

Publication Publication Date Title
US11402369B2 (en) Cuvette-based apparatus for blood coagulation measurement and testing
JP4362532B2 (en) Disposable chamber for analyzing biological fluids
JP2937568B2 (en) Self-measuring fluid analyzer
US7008799B1 (en) Analytical test element with a capillary channel
RU2497100C2 (en) Frustrated total internal reflection biosensor container
US9339815B2 (en) Diagnostic cartridge and control method for diagnostic cartridge
JP2007504438A (en) Sampling device using capillary action
US9201059B2 (en) Microfluidic system and a method of performing a test
US5975153A (en) Capillary fill test device with improved fluid delivery
US20050153457A1 (en) Test strip qualification system
US9933348B2 (en) Sequential aliqoting and determination of an indicator of sedimentation rate
US20100307617A1 (en) Flow cell
CZ2003282A3 (en) Process and apparatus for detection of presence of a liquid on a test strip
JP2014515494A (en) Capillary liquid flow measurement and capillary flow apparatus therefor
US8409413B2 (en) Sampling device for liquid samples
KR101816933B1 (en) Bio sensor and Processing method of the same
US8501112B2 (en) Body fluid analysis fixture
US10661270B2 (en) Disposable cartridge system for point-of-care testing
CA2580810A1 (en) Biological test strip
CZ20022967A3 (en) Apparatus for determining analyte concentration and method of using thereof
EP3722000B1 (en) Fluid delivery method and analysis device
JP5507991B2 (en) applicator
CZ20002021A3 (en) Analytic testing element with capillary channel

Legal Events

Date Code Title Description
AS Assignment

Owner name: INTERNATIONAL TECHNIDYNE CORPORATION,NEW JERSEY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:COLELLA, GREGORY M.;HUANG, HENRY D.;SHISHKIN, DIMITRI;AND OTHERS;SIGNING DATES FROM 20090928 TO 20090929;REEL/FRAME:023368/0758

AS Assignment

Owner name: COMERICA BANK, CALIFORNIA

Free format text: INTELLECTUAL PROPERTY SECURITY AGREEMENT;ASSIGNOR:INTERNATIONAL TECHNIDYNE CORPORATION;REEL/FRAME:026079/0301

Effective date: 20110322

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION

AS Assignment

Owner name: INTERNATIONAL TECHNIDYNE CORPORATION, NEW JERSEY

Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:COMERICA BANK;REEL/FRAME:032123/0787

Effective date: 20140123

AS Assignment

Owner name: INSTRUMENTATION LABORATORY COMPANY, MASSACHUSETTS

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:INTERNATIONAL TECHNIDYNE CORPORATION;REEL/FRAME:047336/0900

Effective date: 20181017