CA2307623C - Serpentine electrophoresis channel with self-correcting bends - Google Patents

Serpentine electrophoresis channel with self-correcting bends Download PDF

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Publication number
CA2307623C
CA2307623C CA002307623A CA2307623A CA2307623C CA 2307623 C CA2307623 C CA 2307623C CA 002307623 A CA002307623 A CA 002307623A CA 2307623 A CA2307623 A CA 2307623A CA 2307623 C CA2307623 C CA 2307623C
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channel
alpha
curved
segments
channel portion
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CA2307623A1 (en
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Eric S. Nordman
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Applied Biosystems Inc
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PE Corp
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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/447Systems using electrophoresis
    • G01N27/44704Details; Accessories
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/447Systems using electrophoresis
    • G01N27/44756Apparatus specially adapted therefor
    • G01N27/44791Microapparatus
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/26Conditioning of the fluid carrier; Flow patterns
    • G01N30/28Control of physical parameters of the fluid carrier
    • G01N2030/285Control of physical parameters of the fluid carrier electrically driven carrier
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/26Conditioning of the fluid carrier; Flow patterns
    • G01N30/38Flow patterns
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/60Construction of the column
    • G01N30/6095Micromachined or nanomachined, e.g. micro- or nanosize
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S366/00Agitating
    • Y10S366/03Micromixers: variable geometry from the pathway influences mixing/agitation of non-laminar fluid flow

Abstract

A serpentine electrophoresis channel, e.g., for a microchip format, is disclosed. The channel includes pairs of linear segments, e.g., parallel or right-angle segments, each joined by an angled channel region having a first curved channel portion subtending an angle .alpha. f>.alpha.
where .alpha. is the angle between segments in a pair, and a second curved channel portion subtending an angle .alpha. s = .alpha. f-.alpha.. The angles and cross sections of the two channel portions are such that .delta.t f, the time differential of analyte migration at inner and outer tracks in the first curved portion is equal to .delta.t s, the time differential of analyte migration at outer and inner tracks in the second curved portion, respectively.

Description

SERPENTINE ELECTROPHORESIS CHANNEL
WITH SELF-CORRECTING BENDS
Field of the Invention 5 The present invention relates to electrophoretic separation devices, and in particular, to a device having a serpentine separation channel, for example, in a microfabricated device.
Background of the Invention Electrophoresis exploits the differential rate of migration of charged species through a l0 separation medium, under the influence of an electric field, for purposes of separating and/or characterizing physical properties of the charged species. Typically, the sample containing the charged species to be separated is placed at one end of a separation channel (which may be a linear channel or a lane in a 2-dimensional slab) and a voltage difference is placed across opposite channel ends until a desired migration end point is reached. The separated analyte 15 molecules may then be detected, e.g., by optical detection, radiography, or band elution.
As examples, gel electrophoresis in the presence of a charged surfactant, such as dodecyl sulfate, is widely used for protein separation and for characterizing protein molecular weight. Electrophoresis in a gel or liquid medium is commonly used to separate oligonucleotides with different numbers of bases, for example, in DNA
sequencing.
20 One of the possible applications of microfabrication techniques that has been proposed is in the area of column separation devices, including electrophoresis devices. 3acobsen, et al.
(Anal. Chem. 66:2369 (1994); Electrophoresis 16:481 (1995) have described a "microchip"
electrophoresis device formed by etching an open electrophoresis channel, and suitable connecting reservoirs, on a glass slide. Because of the small chip dimensions, typically less 25 than 10-15 cm on a side, it is necessary to form the separation column in the form of a serpentine pathway in order to achieve total column separation lengths suitable for most applications.
Although a serpentine column solves the problem of adequate column length on a microchip, it introduces a potentially serious limitation in terms of column resolution. When a 30 electrophoretic band is migrating through a linear channel, the molecules making up the band, which are all migrating at roughly the same speed, tend to migrate as a tight band. However, the same molecules migrating through a tum in a serpentine pathway will migrate through the shorter inner side of the channel faster than through the longer outer side of the channel, leading to band spreading and nonuniformity across the width of the channel.
At each turn in 35 the pathway, more band resolution is lost. Heretofore, this problem has severely limited the range of practical electrophoresis applications in a microchip format.
Summary of the Invention The application includes, in one aspect, an electrophoresis channel through which one or more charged species are intended to migrate under the influence of a voltage difference placed across opposite ends of the channel. The channel includes (i) a pair of channel segments disposed at an angle a with respect to one another, and (ii) an angled channel region connecting the two channel segments.
The angled channel region has a first curved channel portion subtending an angle of>a where a is the angle between the two channel segments, and a second curved channel portion subtending an angle as a,--a,. The first curved portion defines inner and outer tracks or channel sides, such that an analyte migrating through the first channel portion under the influence of such voltage difference will traverse the inner track in a time interval 8tffaster than that of the same analyte traversing the outer track. The second curved portion defines second inner and outer tracks such that an analyte migrating through the second channel portion under the influence of the same voltage difference will traverse the outer track in a time interval Sts, faster than that of the same analyte traversing the inner track. The angles and cross-sections of the two channel portions are such that 8tf is approximately equal to BtS.
The channel is typically part of a serpentine pathway containing a plurality of such segments, each pair of adjacent channel segments being connected by an associated angled channel region.
Where the two channel segments are disposed at right angles with respect to one another, afis preferably between about 110° and 160°, and as, between about 20° and 70°, respectively. Where the two channel segments are disposed substantially parallel to one another, of is preferably between about 200° and 250°, and as, between about 20° and 70°, respectively.
In a microfabricated chip format, the channel has preferred width dimensions between about 25-250 microns, and preferred depth dimensions between about 5-100 microns.
In one general embodiment, the first and second curved portions have substantially constant channel widths W f and WS, respectively, where W'f <Ws. In this embodiment, the angled channel region further includes tapered-width segments joining the second curved channel portion to the first channel portion and to one of the two channel segments. An approximate relationship between Wf and WS, is given by the relationship Wf and WS is given by the relationship WS (afWf R~/a SRS)", where Rf and RS, are the radii of curvature of the first and second curved portions, respectively.

W another general embodiment, the first curved channel portion has a preferably fixed channel width, and the second channel portion, a variable width that expands on progressing inwardly from each end.
In yet another embodiment, the first curved channel portion has a channel depth which increases on progressing toward the second channel portion, and the second curved channel portion has a channel depth which decreases on progressing away from the first curved channel portion. The channel width may be substantially constant in the channel segments and the channel connecting region therebetween.
More generally, the invention includes an analyte separation channel through which one or more analytes is intended to migrate under the influence of a motive force applied to opposite ends of the channel. The device includes (i) a pair of channel segments disposed at an angle a with respect to one another, and (ii) an angled channel region of the type just described connecting the two channel segments. The motive force may be a voltage difference applied across the opposite ends of the channel, or a force producing fluid movement through the channel or a combination of the two.
In a related aspect, the invention includes a microfabricated device for electrophoretic separation of analytes in a mixture. The device includes a substantially planar-surface substrate having formed thereon, first and second reservoirs and a serpentine electrophoretic channel extending therebetween. The channel has a plurality of linear segments, and connecting the adjacent ends of each pair of adjacent segments, an angled channel region of the type described above. The channel, including the linear segments and angled channel regions, has preferred channel width dimensions between about 25-250 microns, and depth dimensions between about 5-100 microns.
According to one aspect of the invention, there is provided an analyte separation device having a substrate in which is formed a channel through which one or more analytes are intended to migrate under the influence of a motive force across the channel, the channel comprising:
(i) a pair of channel segments disposed at an angle a with respect to one another, and (ii) an angled channel region connecting the two channel segments, the region having (a) a first curved channel portion subtending an angle of>a, and defining first inner and outer tracks such that an analyte migrating through the first channel portion under the influence of such force will traverse the inner track in a time interval 8tf faster than that of the same analyte traversing the outer track, and (b) a second curved channel portion subtending an angle as = a,-a, and defining second inner and outer tracks such that an analyte migrating through the second channel portion under the influence of the same force will traverse the outer track in a time interval 8t~

faster than that of the same analyte traversing the inner track, where the cross-sections of the curved channel portions are such that 8tf is approximately equal to Sts.
These and other objects and features of the invention will become more fully apparent when the following detailed description of the invention is read in conjunction with the accompanying drawings.
Brief Description of the Drawings Fig. 1 is a perspective view of a microfabricated device constructed according to the present invention, having an open electrophoresis channel and liquid reservoirs formed on a substrate;
Fig. 2 is an enlarged view of a 180° bend in a serpentine channel formed in accordance with the present invention, illustrating the effect of the self correcting bend on band distortion;

3a Figs. 3A-3C are sectional views taken along lines 3A-3A, 3B-3B, and 3C-3C, respectively, in Fig. 2;
Fig. 4 is an enlarged view of a 900 bend in a serpentine channel formed in accordance with one embodiment of the present invention;
Fig. 5 is an enlarged view of a 900 bend in a serpentine channel formed in accordance with another embodiment of the invention;
Fig. 6 is an enlarged view of a 900 bend in a serpentine channel formed in accordance with yet another embodiment of the invention; and Fig 7 is a cross-section of the channel region in Fig. Ei, taken along the channel pathway 7-7 in Fig. 6.
Detailed Description of the Invention Fig. 1 shows a microfabricated device 10 constructed in accordance with the invention, for electrophoretic separation and/or characterization of one or more analytes in a sample mixture. The device generally includes a planar substrate 12 having formed in its upper surface 14, open reservoirs 16, 18, 19, and 20, and a serpentine electrophoresis channel 22 connecting the reservoirs. Reservoirs 16 and 18, which are intended to contain electrophoresis buffer and sample fluid, respectively, are connected in fluid communication with each other and with channel 22 through a fork-like connector 24.
Reservoirs 19, 20 are intended to hold the waste reservoir. The four reservoirs are connected to electrodes 26, 28, 21, and 30, as shown, which are in turn connected to suitable voltage leads during operation of the device, for (i) loading sample from reservoir 16 into channel 22, by applying a voltage across electrodes 26, 28, and (ii) electrophoretically separating charged sample components, by applying a voltage difference across opposite ends of the channel, i.e., across electrodes 21, 30.
With continued reference to Fig. 1, channel 22 includes a plurality of parallel linear channel segments, such as segments 32, 34, and 36, and curved channel regions connecting the adjacent ends of adjacent linear segments, such as curved channel region 38 connecting adjacent ends of segments 32, 34. In a typical embodiment, the substrate or chip has side dimensions of between about 1 to 15 cm, and the linear segments are each about .5 to 10 cm in length. Thus, for example, a channel having 30 linear segments, each about 8 mm in length has a column length, ignoring the lengths of the connecting regions, of about 250 mm. With the added lengths of the connecting regions, the total length may be in the 30 cm range, on a chip whose side dimensions may be as little as 1 cm. A coverslip 23 t>laced over the portion of the substrate having the serpentine channel serves to enclose the channel, although an open serpentine channel is also contemplated.
The construction of a curved connecting region-- in this case, region 38-- is shown in enlarged plan view in Fig. 2, which shows portions of linear segments 32, 34 connected by the region. The region includes a first curved channel portion 40 which subtends an angle of 5 which is greater than the minimum angle a needed to connect the two segments. Where, as here, the linear segments are parallel and a is 180°, of is typically between about 200°-250°, i.e., about 20°-70° over the minimum angle. As shown, portion 40 has a substantially constant channel width W f along its length, equal to the channel width of the connected linear segments.
10 As seen in Fig. 3A, which is a cross-section along line 3A-3A in Fig. 2, the channel has a substantially rectangular cross-section with a width dimension Wf and depth dimension df. W f is typically between about 25-200, preferably 50-100 microns, and df is typically about 5-100, preferably 25-75 microns.
W ith continued reference to Fig. 2. portion 38 includes a second curved channel 15 portion 42 subtending an angle aS which corrects the overangle of to provided the desired 180°
total angle in the curved portion; that is, as a~-a. Thus, for example, where a is I 80°, and of is between about 210° and 250°, aS is between about 20°
and 70°, respectively. The width WS
of the second curved portion is greater than Wf and is selected, in relation to the two angles of and as, and in accordance with the invention, to correct band distortion produced as a band 20 moves through portion 40, as will be described below. In the embodiment illustrated, and as shown in Fig. 3C, WS is greater than Wf, acting in effect reduce the electric field strength on analyte molecules migrating through this portion, relative to portion 40. As seen in Fig. 3C, the channel depth d5 in portion 42 is the same as that in portion 40, i.e., d5 df.
Channel region 38 further includes two tapered-width segments 44, 46, which serve as 25 interfaces between (i) the smaller-width portion 40 and the larger-width portion 42 (segment 44) and between (ii) the larger-width portion 42 and the smaller-width linear segment 34 (segment 46). A cross-sectional view of segment 44 is shown in Fig. 3B, showing a channel width intermediate between that of portions 40, 42, and the same channel depth.
The operation of the second channel portion, in correcting curved channel effects 30 produced in the first channel portion, will now be discussed, also with reference to Fig. 2. In this figure, a charged species migrating as a band through the channel is indicated at various stages through the curved channel regions by numerals 48a-48g. Band 48a, which is at the position just entering the curved channel portion, is substantially undistorted, meaning that the band is both narrow and disposed along an axis substantially normal to the channel axis. As the band enters channel portion 40, it begins to distort, as shown at 48b, due to the shorter migration distance of molecules along the inner track 40a and the longer migration distance of molecules along the outer track 40b. The distortion increases progressively as the band migrates through portion 40, as illustrated by bands 48c and 48d.
5 It can be shown that a band on the inside track will lead a band on the outside track with a time 8f approximately equal to a~(2W~R,~)/pEf.~"«<, where Rf is the radius of curvature of curved portion 40, W f is the channel width, p is the mobility of the migrating species, in m2/Vsec, and Ef~~",~r is the electric field in portion 40 at the center of the track, resulting from the potential difference applied across opposite ends of the channel.
10 The purpose of the second curved portion is to provide a correction, on the opposite channel side, for the band distortion produced in the first curved portion.
Briefly, this second curved portion is designed such that a band on the outside track 42b (which is now the shorter of the two tracks) will lead the band on the inside track 42a by a time 85 substantially equal to 8f. Similar to the calculation above, it can be shown that 85 is approximately equal to 15 as(2WSR5)/uEf.~~°«" where Rs is the radius of curvature of curved portion 42, Wf is the channel width, p is the mobility of the migrating species, in m'-/Vsec, and Ef~~°,e~ is the electric field in portion 42 at the center of the track, also due to the same potential difference applied across the ends of the channel. It is noted that E,~~",tt is less than Ef~",tt, due to the larger channel width in channel 42, according to the relationship ES E~WfJWs). The condition 885 is 20 satisfied when a~(2WfRf.)/pEf~~",tt = as(2WSR5)/gEf_°~"t~, that is, when a~Jas WSZRs/Wf'-Rf. As an example, assume WS is 50 gm, a5 is 210° of is 30°, and R~-Rs=1 mm. WS is then ((50 Itm)2(210/30))"'-, or about 132 um.
With reference again to Fig. 2, it can be appreciated that band 48d migrates through tapered segment 44 substantially without correction, is fully corrected within portion 42, and 25 then migrates through segment 46 and into segment 34 in corrected form, i.e., with the band axis oriented substantially normal to the segment axis.
Fig. 4 shows an embodiment of a 90° curved channel region 50 constructed in accordance with the invention, for use, for example, in a serpentine channel of the type described above, but where each 180° turn is produced by two adjoining 90° turns. Channel 30 region 50 joins two linear channel segments 52, 54 which in this embodiment are disposed at right angles with respect to one another.
Channel region 50 includes a first curved channel portion 56 which subtends an angle of which is greater than 90°, and a second channel portion 58 which subtends an angle as which corrects the overangle of to provide the desired 90° total angle in the curved portion;

that is, as a~-a. In the a=90 embodiment, of is typically between about 110° and 160°, and aS
is between about 20° and 70°, respectively. As in the 180° embodiment, the width WS of the second curved portion is greater than Wf and is selected, in relation to the two angles of and a5, and in accordance with the invention, to correct band distortion produced as a band moves 5 through portion 56, as will be described below. In the embodiment illustrated, where the channel depth is uniform throughout the channel region WS is greater than Wf, and related through the relationship a~(2WfRf)I~Ef~rn,~~= as(2WSRS)/pErt~",tt> or equivalently, when a~Jas WSZRS/We Rf, where Rf, RS, ~, Ef~~",«, and Ef~~~,« are as above. As an example, assume WS is 50 Vim, as is 120° and of is 30°, and Rf=RS=1 mm. WS is then (50 umz(120/30))'', or 100 10 pm.
Region 50 further includes tapered segments 60, 62 which serve as interfaces between (l) the smaller-width portion 56 and the larger-width portion 58, and (ii) the larger-width portion 42 and the smaller-width linear segment 54.
Analogous to the band behavior in the 180° turn region 38, an analyte band migrating I S into portion 56, substantially normal to the axis of segment 52, will become distorted by its migration through portion 56, with the outer-side of the band trailing the inner side of the band. The analyte migrates through tapered segment 60 substantially without correction, is fully corrected within portion 58 and then migrates through segment 62 and into segment 54 in corrected form, i.e., with the band axis oriented substantially normal to the segment axis.
2o Fig. 5 shows another embodiment of a 90° curved channel region 64 constructed in accordance with the invention, for use, for example, in a serpentine channel 66 of the type described above. Channel region 64 joins two linear channel segments 68, 70 which in this embodiment are disposed at right angles with respect to one another. Channel region 50 includes a first curved channel portion 72 subtending an angle of which is greater than 90°, 25 and a second channel portion 74 subtending an angle aS which corrects the overangle of to provided the desired 90° total angle in the curved portion.
This embodiment differs from the one illustrated in Fig. 4 in that curved portion 74 replaces portion 58 and the two tapered segments 60, 62 in portion 50, as a continuously curved portion. That is, WS is continuously variable through portion 74, from a minimum 30 width WS to a maximum width WS_ma,~. Exemplary angles as, af, are as above, where the radius of curvature RS of portion 74 is about 3-4 times that in the Fig. 4 embodiment, but the angle as subtending the portion is about the same in both embodiments. The relationship between WS
and Wf is more complex than that shown above, but can be determined from the relationships given above, by integrating over as, where the value of WS varies continuously over portion 74 according to a known angle-dependent relationship.
The operation of portion 74 in correcting band distortion produced in portion 72 is substantially as described above, but where band correction occurs over the entire region between portion 72 and segment 70.
5 Still another embodiment of the invention, for a 90° turn, is illustrated by angle channel region 76 in Fig. 6. The channel region, which joins right-angle channel segments 78, 80, includes a first curved channel portion 82 subtending an angle a~90°, and a second curved channel portion 84 subtending an angle as, which corrects the overangle of to provided the desired 90° total angle in the curved portion. Also forming part of the channel region are 10 interface segments 86, 88 connecting portion 82 to portion 84, and portion 84 to segment 80, respectively. Exemplary of and as are as above.
The embodiment differs from those above in that the width Wf of portion 84 is the same the width WS of portion 82, but portion 84 has a depth d5 which is greater than df, as illustrated in Fig. 7, which shows a segmented cross-section (through segments indicated by A, 15 B, C, D, and E) along indicated portions of region 76. Also as seen, interface segments 86, 88 have tapered channel depths, rather than the tapered channel widths of the interface segments in the earlier described embodiments.
The electric field ES in portion 84 is equal to E~(d~/df), and band correction (st~st~
occurs when a~(ZWfR,.)/p.Ef~~",« as(2WSR$)~pESK~n~tt, that Is, when 2o a~JaS WSdSRs/WtdfR~--d5R5JdfRf.. As an example, assume d5 is 50 pm, as is 120° and of is 30°, and Rf=Rs=1 mm. WS is then 50 p.m (120/30), or about 200 Vim.
The operation of region 76 in correcting band distortion is similar to that described above, for example, with respect to the embodiment shown in Fig. 4. Briefly, a band becomes distorted by its migration through portion 82, with the outer-side of the band trailing the inner 25 side of the band. The band migrates through tapered segment 86 substantially without correction, is fully corrected within portion 84 and then migrates through segment 88 and into segment 80 in corrected form, i.e., with the band axis oriented substantially normal to the segment axes.
From the foregoing, it can be appreciated how various objects and features of the 30 invention are met. The invention is compatible with tightly coiled serpentine electrophoresis or other chromatographic channel configurations formed in a small-area microchip, for example, using conventional microfabrication techniques. The microfabrication method may involve either same-depth, variable-width etching, or same-width, variable depth etching, or a combination of the two.

The self correcting bend feature of the invention acts to correct distortion produced by band migration around a tum, due to slower migration at the outside of the turn, acting to preserve band resolution along the entire channel length, which may include numerous turns, typically 90° or 180° turns.
5 Although the invention has been described with respect to specific embodiments, it will be appreciated that a variety of modifications may be made within the scope of the claimed invention. For example, the serpentine channel may be formed by chemical or laser etching techniques on a relatively large-scale plate, e.g., a 10 cm x 10 cm plate designed for preparative electrophoresis or chromatography. The serpentine channel may be formed in a 10 closed tube, such as a capillary electrophoresis tube, where each turn in the tube includes an expanded diameter, self correcting counter turn. In still another aspect, the self correcting turn may apply to other types of chromatography channels or tubes, dependent on pressurized fluid flow or gravity rather than a voltage difference as a motive force for moving analyte molecules through a separation medium.

Claims (12)

IT IS CLAIMED:
1. An analyte separation device having a substrate in which is formed a channel through which one or more analytes are intended to migrate under the influence of a motive force across the channel, said channel comprising:
(i) a pair of channel segments disposed at an angle .alpha. wrath respect to one another, and (ii) an angled channel region connecting the two channel segments, said region having (a) a first curved channel portion subtending an angle .alpha.1>.alpha. and defining first inner and outer tracks such that an analyte migrating through the first channel portion under the influence of such force will traverse the inner track in a time interval .delta.t f faster than that of the same analyte traversing the outer track, and (b) a second curved channel portion subtending an angle ,.alpha.s=.alpha.f-.alpha. and defining second inner and outer tracks such that the analyte migrating through the second channel portion under the influence of the same force will traverse the outer track in a time interval .delta.t s faster than that of the same analyte traversing the inner track, where the cross-sections of said curved channel portions are such that .delta.t f is approximately equal to .delta.t s.
2. The device of claim 1, wherein the two channel segments are disposed at right angles with respect to one another .alpha.f is between about 110° and 160°, and .alpha.s, between about 20° and 70°, respectively.
3. The device of claim 1, wherein the channel segments are disposed substantially parallel to one another, of is between about 200° and 250°, and .alpha.s, between about 20° and 70°, respectively.
4. The device of any one of claims 1 to 3 which is formed in a microfabricated chip, and has channel width dimensions between about 25-250 microns, and depth dimensions between about 5-100 microns.
5. The device of any one of claims 1 to 4, which is part of a serpentine pathway containing a plurality of such segments, each segment pair connected by said angled channel region.
6. The device of any one of claims 1 to 5, wherein the first and second curved portions have substantially constant channel widths W f and W s, respectively, where W
f<W s, and the angled channel region further includes tapered-width segments joining the second curved channel portion to the first channel portion and to one of the two associated channel segments.
7. The device of claim 6, wherein W s=(.alpha.f W f2R f/.alpha.s R s)~, where R f and R s are the radii of curvature of the first and second curved portions, respectively.
8. The device of any one of claims 1 to 5, wherein the first curved channel portion has a fixed channel width, and the second channel portion, a variable width that expands on progressing inwardly from each end.
9. The device of any one of claims 1 to 5, wherein the first curved channel portion has a channel depth which increases on progressing toward the second channel portion, and the second curved channel portion has a channel depth which decreases on progressing away from the first curved channel portion.
10. The device of claim 9, whose channel width is substantially constant in the channel segments and the channel connecting regions therebetween.
11. The device of any one of claims 1 to 10 for use in electrophoretic separation of analytes in a mixture, wherein said motive force is a voltage difference applied across opposite ends of the channel.
12. A microfabricated device for electrophoretic separation of analytes in a mixture, comprising a substantially planar-surface substrate having formed thereon, (i) first and second reservoirs and (ii) a channel, as defined in any one of claims 1 to 11, extending between said first and second reservoirs.
CA002307623A 1997-11-12 1998-11-12 Serpentine electrophoresis channel with self-correcting bends Expired - Fee Related CA2307623C (en)

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US6510097P 1997-11-12 1997-11-12
US60/065,100 1997-11-12
PCT/US1998/024202 WO1999024828A1 (en) 1997-11-12 1998-11-12 Serpentine electrophoresis channel with self-correcting bends

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CA2307623C true CA2307623C (en) 2004-03-16

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Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU3771599A (en) 1998-05-18 1999-12-06 University Of Washington Liquid analysis cartridge
US6830729B1 (en) 1998-05-18 2004-12-14 University Of Washington Sample analysis instrument
US6913679B1 (en) * 1999-02-11 2005-07-05 The Regents Of The University Of California Apparatus and methods for high resolution separation of sample components on microfabricated channel devices
US6270641B1 (en) 1999-04-26 2001-08-07 Sandia Corporation Method and apparatus for reducing sample dispersion in turns and junctions of microchannel systems
US6471392B1 (en) * 2001-03-07 2002-10-29 Holl Technologies Company Methods and apparatus for materials processing
US6742774B2 (en) 1999-07-02 2004-06-01 Holl Technologies Company Process for high shear gas-liquid reactions
US7538237B2 (en) * 1999-07-02 2009-05-26 Kreido Laboratories Process for high shear gas-liquid reactions
JP2001281233A (en) * 2000-03-28 2001-10-10 Inst Of Physical & Chemical Res Microchip for water distribution and water distribution method using it
US6902313B2 (en) * 2000-08-10 2005-06-07 University Of California Micro chaotic mixer
US20020060153A1 (en) * 2000-11-06 2002-05-23 Dna Sciences, Inc. Microchannel turn design
US6830806B2 (en) * 2001-04-12 2004-12-14 Kreido Laboratories Methods of manufacture of electric circuit substrates and components having multiple electric characteristics and substrates and components so manufactured
US6596140B2 (en) 2001-05-01 2003-07-22 Applera Corporation Multi-channel capillary electrophoresis device and method
KR100442681B1 (en) * 2001-05-10 2004-08-02 주식회사 디지탈바이오테크놀러지 Channel unit and apparatus for mixing fluids using the unit
KR100442680B1 (en) * 2001-05-10 2004-08-02 주식회사 디지탈바이오테크놀러지 Apparatus for mixing fluids by micro channel
US6919058B2 (en) * 2001-08-28 2005-07-19 Gyros Ab Retaining microfluidic microcavity and other microfluidic structures
WO2003022415A2 (en) * 2001-09-13 2003-03-20 Holl Technologies Company Methods and apparatus for transfer of heat energy between a body surface and heat transfer fluid
US6787246B2 (en) 2001-10-05 2004-09-07 Kreido Laboratories Manufacture of flat surfaced composites comprising powdered fillers in a polymer matrix
KR100473364B1 (en) * 2001-10-17 2005-03-08 주식회사 디지탈바이오테크놀러지 Microchannel apparatus for mixing liquids using microchannel and method therefor
US7459127B2 (en) * 2002-02-26 2008-12-02 Siemens Healthcare Diagnostics Inc. Method and apparatus for precise transfer and manipulation of fluids by centrifugal and/or capillary forces
US7005301B2 (en) * 2002-06-10 2006-02-28 Sandia National Laboratories Piecewise uniform conduction-like flow channels and method therefor
US20050238506A1 (en) * 2002-06-21 2005-10-27 The Charles Stark Draper Laboratory, Inc. Electromagnetically-actuated microfluidic flow regulators and related applications
US7867193B2 (en) * 2004-01-29 2011-01-11 The Charles Stark Draper Laboratory, Inc. Drug delivery apparatus
US7098360B2 (en) * 2002-07-16 2006-08-29 Kreido Laboratories Processes employing multiple successive chemical reaction process steps and apparatus therefore
AU2003266154B2 (en) * 2002-09-11 2009-01-22 Kreido Laboratories Methods and apparatus for high-shear mixing and reacting of materials
US6938687B2 (en) * 2002-10-03 2005-09-06 Holl Technologies Company Apparatus for transfer of heat energy between a body surface and heat transfer fluid
US7094354B2 (en) * 2002-12-19 2006-08-22 Bayer Healthcare Llc Method and apparatus for separation of particles in a microfluidic device
DE10303107B3 (en) * 2003-01-27 2004-09-16 Sls Micro Technology Gmbh Separation column, in particular for a miniaturized gas chromatograph
WO2004113898A1 (en) * 2003-05-19 2004-12-29 Protasis Corporation Electrophoresis devices and methods for focusing charged analytes
US7435381B2 (en) * 2003-05-29 2008-10-14 Siemens Healthcare Diagnostics Inc. Packaging of microfluidic devices
US7160025B2 (en) * 2003-06-11 2007-01-09 Agency For Science, Technology And Research Micromixer apparatus and methods of using same
US20040265171A1 (en) * 2003-06-27 2004-12-30 Pugia Michael J. Method for uniform application of fluid into a reactive reagent area
US20040265172A1 (en) * 2003-06-27 2004-12-30 Pugia Michael J. Method and apparatus for entry and storage of specimens into a microfluidic device
US20080257754A1 (en) * 2003-06-27 2008-10-23 Pugia Michael J Method and apparatus for entry of specimens into a microfluidic device
JP2005024316A (en) * 2003-06-30 2005-01-27 Kyocera Corp Microchemical chip and manufacturing method therefor
US7347617B2 (en) * 2003-08-19 2008-03-25 Siemens Healthcare Diagnostics Inc. Mixing in microfluidic devices
US20050121324A1 (en) 2003-09-05 2005-06-09 Caliper Life Sciences, Inc. Analyte injection system
US7867194B2 (en) 2004-01-29 2011-01-11 The Charles Stark Draper Laboratory, Inc. Drug delivery apparatus
US20060285433A1 (en) * 2005-06-20 2006-12-21 Jing-Tang Yang Fluidic mixer of serpentine channel incorporated with staggered sudden-expansion and convergent cross sections
US20090268548A1 (en) * 2005-08-11 2009-10-29 Eksigent Technologies, Llc Microfluidic systems, devices and methods for reducing diffusion and compliance effects at a fluid mixing region
US20070246106A1 (en) 2006-04-25 2007-10-25 Velocys Inc. Flow Distribution Channels To Control Flow in Process Channels
US9046192B2 (en) * 2007-01-31 2015-06-02 The Charles Stark Draper Laboratory, Inc. Membrane-based fluid control in microfluidic devices
JP2008212814A (en) * 2007-03-02 2008-09-18 Canon Inc Fluid carrying passage, fluid treatment apparatus and fluid treatment system
US8186913B2 (en) * 2007-04-16 2012-05-29 The General Hospital Corporation Systems and methods for particle focusing in microchannels
JP4411661B2 (en) * 2007-10-26 2010-02-10 セイコーエプソン株式会社 Biological substance detection method
US8430558B1 (en) * 2008-09-05 2013-04-30 University Of Central Florida Research Foundation, Inc. Microfluidic mixer having channel width variation for enhanced fluid mixing
US8377277B2 (en) 2008-10-22 2013-02-19 General Electric Company System and method for performing microfluidic manipulation
JP5008690B2 (en) 2009-03-31 2012-08-22 信和化工株式会社 Microchannel device and method for manufacturing microchannel device
WO2010141131A1 (en) * 2009-06-04 2010-12-09 Lockheed Martin Corporation Multiple-sample microfluidic chip for dna analysis
AU2011305254B2 (en) * 2010-09-26 2014-06-05 Da Yu Enterprises, L.L.C. Separation of analytes
AU2011315951B2 (en) 2010-10-15 2015-03-19 Lockheed Martin Corporation Micro fluidic optic design
WO2012106501A1 (en) 2011-02-02 2012-08-09 The Charles Stark Draper Laboratory, Inc. Drug delivery apparatus
US8795605B2 (en) * 2012-01-12 2014-08-05 Fred C. Senftleber Apparatus and methods for transferring materials between locations possessing different cross-sectional areas with minimal band spreading and dispersion due to unequal path-lengths
US9322054B2 (en) 2012-02-22 2016-04-26 Lockheed Martin Corporation Microfluidic cartridge
CN102788831B (en) * 2012-08-13 2014-07-30 中国科学院研究生院 Microfluidic chip electrophoretic-electrochemical detecting device with adjustable pH after separation and use thereof
US20140065034A1 (en) * 2012-08-31 2014-03-06 Yun Zheng Microfluidic device and method of fabricating microfluidic devices
CN106596692B (en) * 2017-01-14 2018-12-28 常州大学 A kind of method of tortuous capillary electrophoresis detection antibody polypeptides interaction
WO2022241247A1 (en) * 2021-05-13 2022-11-17 Fluid-Screen, Inc. Microfluidic device with improved flow profile

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0339780B1 (en) * 1988-04-29 1996-08-28 Beckman Instruments, Inc. Capillary detector cartridge for electrophoresis
JPH03223674A (en) * 1989-11-30 1991-10-02 Mochida Pharmaceut Co Ltd Reaction vessel
SE470347B (en) * 1990-05-10 1994-01-31 Pharmacia Lkb Biotech Microstructure for fluid flow systems and process for manufacturing such a system
WO1993022058A1 (en) * 1992-05-01 1993-11-11 Trustees Of The University Of Pennsylvania Polynucleotide amplification analysis using a microfabricated device
DE59410283D1 (en) 1993-11-11 2003-06-18 Aclara Biosciences Inc Device and method for the electrophoretic separation of fluid substance mixtures
US6001229A (en) 1994-08-01 1999-12-14 Lockheed Martin Energy Systems, Inc. Apparatus and method for performing microfluidic manipulations for chemical analysis
US5658413A (en) * 1994-10-19 1997-08-19 Hewlett-Packard Company Miniaturized planar columns in novel support media for liquid phase analysis
JP3839524B2 (en) * 1995-06-07 2006-11-01 アジレント・テクノロジーズ・インク Miniaturized total analysis system
US5993750A (en) * 1997-04-11 1999-11-30 Eastman Kodak Company Integrated ceramic micro-chemical plant
US5958694A (en) * 1997-10-16 1999-09-28 Caliper Technologies Corp. Apparatus and methods for sequencing nucleic acids in microfluidic systems

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