SEPARATION AND ANALYSIS OF SAMPLES BYMICROFLUIDIC FREE-FLOW ELECTROPHORESIS

Abstract

A microfluidic device (11) is provided for separation and analysis of microfluidic samples. The device comprises: a separation channel (10); a first electrolyte channel (12) configured to provide a flow of high conductivity electrolyte solution, in use; and provided with a positive electrode (13) at a downstream outlet of the channel; a second electrolyte channel (14) configured to provide a flow of high conductivity electrolyte solution, in use, and provided with a negative electrode (15) at a downstream outlet of the channel; and wherein the flow of electrolyte through the first and second electrolyte channels removes electrophoresis products and gas bubbles from the device; and wherein the presence of the electrolyte provides a substantially homogenous electric field across the separation channel.

Claims

1. A microfluidic device for separation and analysis of microfluidic samples, the device comprising a separation channel; a first electrolyte channel configured to provide a flow of high conductivity electrolyte solution, in use; and provided with a positive electrode at a downstream outlet of the channel; a second electrolyte channel configured to provide a flow of high conductivity electrolyte solution, in use, and provided with a negative electrode at a downstream outlet of the channel; and wherein the flow of electrolyte through the first and second electrolyte channels removes electrophoresis products and gas bubbles from the device; and wherein the presence of the electrolyte provides a substantially homogenous electric field across the separation channel.

2. The microfluidic device according to claim 1 or claim 2, wherein the positive and negative electrodes are solely located at the downstream outlet of the respective channel.

3. The microfluidic device according to claim 1 or claim 2, wherein the first and second electrolyte channels are connected to the separation channel by an array of conducting channels.

4. The microfluidic device according to claim 3, wherein the array of conducting channels comprises at least one conducting channel which is located adjacent to the inlet of the separation channel.

5. The microfluidic device according to claim 3 or claim 4, wherein the array of conducting channels comprises at least one conducting channel which is located adjacent to the outlet of the channel.

6. The microfluidic device according to any one of claims 3 to 5, wherein the array of conducting channels is substantially coterminous with the separation channel.

7. The microfluidic device according to any one of the preceding claims, wherein the array of conducting channels is substantially perpendicular to the separation channel and the first and second electrolyte channels.

8. The microfluidic device according to any one of the preceding claims, wherein the array of conducting channels is configured to provide an electrical connection between the separation channel and the electrodes.

9. The microfluidic device according to claim 8, wherein the electrolyte that flows through the conducting channels contributes between 0.1% and 10% of the total fluid flow through the separation channel.

10. The microfluidic device according to any one of the preceding claims, wherein the electrolyte solution is a high conductivity electrolyte solution.

11. The microfluidic device according to any one of the preceding claims, wherein the positive and negative electrodes are metallic connectors.

12. The microfluidic device according to any one of claims 1 to 11, wherein the separation channel has multiple outlets.

13. A method of analysing a sample devoid of electrolysis products in a microfluidic device according to any one of claims 1 to 12; the method comprising the steps of: flowing high conductivity electrolyte solution through the first and second electrolyte channels; flowing a sample through the separation channel; taking an optical image of the separation channel; and analysing the optical image of the separation channel.

14. A method of separating a first sample in a microfluidic device according to claim 12; the method comprising the steps of: flowing high conductivity electrolyte solution through the first and second electrolyte channels; flowing a microfluidic sample through the separation channel; sampling the output from at least one of the outlets from the separation channel.

15. The method according to claim 13 or claim 14, wherein the electrolyte solution and microfluidic sample flow in the same direction inside the separation channel.

16. The method according to claim 14 or claim 15, wherein heat is removed from the microfluidic device by the flow of high conductivity electrolyte solution.

17. The method according to any one of claims 13 to 16, wherein gas bubbles are removed from the microfluidic device by the flow of high conductivity electrolyte solution.

18. The method according to any one of claims 13 to 17, wherein the electric current flows substantially opposite to the flow of the electrolyte solution in the first electrolyte channel.

19. The microfluidic method according to any one of claims 13 to 18, wherein the electrolyte solution forms an interface with a separation medium resulting in a liquid electrode.

20. The microfluidic method according to any one of claims 13 to 19, wherein the electrolyte solution is potassium chloride.

21. The microfluidic method according to claim 18, wherein the separation medium is a buffer solution.

22. The microfluidic method according to claim 21, wherein the buffer solution is selected from a group including a Good's buffer, a phosphate buffer, PBS, carbonate buffer and borate buffer.

Description

[0029] The invention will now be further and more particularly described, by way of example only, and with reference to the accompanying drawings, in which:

[0030] FIG. 1 shows (a) and (c) drawings and (b) and (d) schematic diagrams of microfluidic devices according to the present invention,

[0031] FIG. 2 provides microfluidic electrophoresis images of fluorescein and rhodamine,

[0032] FIG. 3 shows microfluidic electrophoresis of lysozyme molecules,

[0033] FIGS. 4 and 5 shows plots of current versus applied voltage (I-V curves) of electrolyte solution in the electrolyte channels,

[0034] FIGS. 6 and 7 illustrates the separation of samples in the separation channel,

[0035] FIG. 8 provides an image of bubbles flowing out of the microfluidic device,

[0036] FIG. 9 shows a decoupled, connectable flow control for the recycling of high conductivity solutions.

[0037] The present invention relates to the separation and analysis of microfluidic samples using free-flow electrophoresis in microfluidic devices.

[0038] Referring to FIG. 1, there is provided a microfluidic device 11 for separation and analysis of microfluidic samples, the device 11 comprising a separation channel 10; a first electrolyte channel 12 provided with a positive electrode 13 at a downstream outlet of the channel; a second electrolyte channel 14 provided with a negative electrode 15 at a downstream outlet of the channel. The first 12 and second 14 electrolyte channels are configured to provide a homogenous electric field across the separation channel 10.

[0039] As illustrated in FIG. 1, the separation of samples takes place in the separation channel 10. Microfluidic samples may be proteins, or nucleic acids or fluorescent particles such as fluorescein and rhodamine particles (FIGS. 2 and 5). In some instances, the sample may comprise charged particles. In one example, charged particles can be separated under the application of an electric field within the microfluidic device.

[0040] The separation channel 10 shown in FIG. 1 is connected by an array of conducting channels 16, which, together with the electrolyte channels, provides a high conductivity electrolyte solution to transport the electric current from the downstream electrodes to the separation channel.

[0041] The array of conducting channels 16 may establish an electrical connection between the positive electrode 13 and negative electrode 15 with the separation channel 10, whilst also providing a high hydrodynamic resistance to minimise mass transfer between the channels.

[0042] In order to generate a narrow beam of analyte, the microfluidic sample containing oppositely charged particles and a solution of buffer (typically, 0.5-50 mM phosphate buffer) flows into the separation channel 10 through a first inlet channel 18 and a second inlet channel 19, respectively. In addition, an electrolyte solution flows into the first electrolyte channel 12 and the second electrolyte channel 14. Preferably, the electrolyte solution is a high conductivity solution. For example, the electrolyte solution may be KCl solution. A high concentration of KCl solution can be flowed into the electrolyte channels by means of a syringe pump or by pressurising a fluid reservoir.

[0043] As used herein, and unless otherwise specified, the term analyte refers to a sample, component or particle of a substance that is of interest in an analytical or separation based procedure.

[0044] As used herein, and unless otherwise specified, the term separation channel refers to any channel through which a sample fluid is flowed which is subject to an electric field. In some embodiments, there are multiple outlets to the separation channel and, in these examples, the channel is used to separate different components of the fluid, which components are then removed through different outlets from the separation channel. In some embodiments, the separation channel is used for analytical purposes only and the separation of the fluid arising from the application of the electric field provides for the in situ analysis of the sample. The provision of one or more outlets is not critical to the analysis function, as this is carried out whilst the sample remains in the separation channel.

[0045] A flow rate of fluids, such as the flow rate of an electrolyte solution, may be established in the electrolyte channels. The flow rate, typically in the order of a few hundred microliters per hour, in the electrolyte channels were higher by 10% than in the separation channel, thereby forcing, together with the hydrodynamic resistance at the end of the electrolyte channels, the KCl solution through the conducting channels and forming two thin sheets of KCl at the edge of the separation channel.

[0046] As shown in FIG. 1, the positive electrode 13 at the downstream outlet of the first electrolyte channel 12 and the negative electrode 15 at the downstream outlet of the second electrolyte channel 14 are connected to a voltage source 20. Preferably, the positive 13 and negative 15 electrodes are metallic connectors. The metallic connectors may be hollow.

[0047] Upon application of a voltage to the metallic connectors 13, 15, the high conductivity KCl solution transmits the current and thus applies an electric field, typically a homogenous electric field, to the separation channel against the direction of the electrolyte flow at the side of the positive electrode.

[0048] At the same time, gas bubbles formed at the interface of metal connectors and KCl solutions as well as heat and electrolysis products, are directly transported out of the microfluidic device and would be discharged from the device directly without getting in contact with the separation channel and without disturbing the fluid flows. As shown in FIG. 8, gas bubbles 25, electrolysis products and heat, such as joules heat, can be transported out of the device using a tube of approximately 1 to 5 mm in diameter. Each of the bubbles produced may be around the same volume as all of the fluids in the microfluidic channels.

[0049] The high conductivity electrolyte solution may form a stable interface with the separation medium, thus effectively acting as a liquid electrode carrying the electric current. Due to the ability of ions to cross this interface however, no electrochemical reactions take place inside or adjacent to the separation channel.

[0050] In some embodiments, the separation medium can be an auxiliary fluid such as a buffer solution, for example phosphate buffer. Typically, 0.5 to 50 mM of phosphate buffer is used, or it may exceed 5, 10, 15 or 25 mM. In some embodiments, the concentration of phosphate buffer used may be less than 50, 40, 30 or 20 mM. Preferably, 10 mM phosphate buffer is used. The auxiliary fluid may be in the separation channel into which the charged particles are flown.

[0051] The width of the separation channel may be 0.25 to 50 mm, or it may exceed 1, 5, 10 or 15 mm. The width of the separation channel may be less than 7.5, 5, 2.5 or 1 mm. For example, the width of the separation channel may be 2 mm or 10 mm.

[0052] The width of the first and second electrolyte channels may be 0.2 to 10 mm, or it may exceed 2.5, 5 or 7.5 mm. The width of the first and second electrolyte channels may be less than 10, 7.5 or 5 mm. Preferably, the width of the electrolyte channels are 1 mm.

[0053] The length of the separation channel, the first and second electrolyte channels can be approximately 2 to 100 mm, or it may exceed 5, 10 or 15 mm. The length of the separation channel and the electrolyte channels may be less than 20, 15, 10 or 5 mm. For example, the length of the separation channel and the electrolyte channels may be approximately 5 mm or, it may be approximately 25 mm.

[0054] The length of the conducting channels may be 0.1 to 15 mm, or it may exceed, 1, 2, 5, 7, or 10 mm. The length of the conducting channels may be less than 15, 12, 7.5 or 5 mm. Preferably, the length of the conducting channels is approximately 2 mm.

[0055] The height of the separation channel, electrolyte channels and the conducting channels can be approximately 5 to 250 m, or it may exceed 15, 25 or 35 m. The height of the separation channel, the electrolyte channels and the conducting channels may be less than 100, 20 or 10 m. Preferably, the height of the separation channel, the electrolyte channels and the conducting channels is approximately 25 m. With these dimensions, the analyte may remain in the separation channel for approximately 1.5 seconds at a typical flow rate of 600 L/h.

[0056] FIGS. 1(a) and (b) show an embodiment that is optimised for analysis of a sample and is provided with only a single outlet 23 from the separation channel 10. In contrast, FIGS. 1(c) and 1(d) show an embodiment that is optimised for separation of a sample and is therefore provided with three outlets 23 from the separation channel 10. This configuration allows three separate fractions of the sample to be collected at the three outlets and can also be used for analysis of a sample inside the separation channel. It will be understood that the number of outlets 23 can be selected to optimise performance depending on the type of separation and the extent of separation required. A single outlet 23 is most appropriate when analysis is based on the distribution of the sample within the channel, for example as obtained using a fluorescent marker and viewing the distribution of the sample under fluorescent light within the channel. Where different fractions from the sample are separated and subsequently measured, analysed or treated differently then the number of fractions required will dictate the optimum number of outlets. For example, two, three, four or more outlets may be provided.

[0057] Referring to FIGS. 2, 3, 4, 5, 6 and 7 the separation and analysis of samples such as fluorescent particles and proteins are illustrated. The separation of particles in the microfluidic device may utilise an electrophoretic method. Typically, the electrophoretic method is a free-flow electrophoretic method.

[0058] As illustrated in FIGS. 2 and 5, the microfluidic device as disclosed in this invention may be used to separate fluorescent particles such as fluorescein and rhodamine. In one example, a mixed solution of 10 g/ml fluorescein and 10 g/ml rhodamine in 10 mM KCl (pH=7.0) was injected into the separation channel, flanked by a 10 mM KCl solution, and a 1 M KCl solution was injected into the electrolyte channels (with 10 g/ml fluorescein to be able to monitor the flow of the high conductivity solution through the array of conducting channels). The results are shown in FIG. 2. Under high flow rates of a total of 600 L/h in the separation channel, a clear deflection and separation of the two oppositely charged analytes can be seen in the images. The ratio between the sample stream separation and the width of the streams was about 7 at an applied voltage of 40 volts. The I-V curves in FIGS. 4 and 5 show that the deflection with voltage and electric field exhibit linear relationship. With these data and the device characteristics, the electrophoretic mobility of fluorescein was calculated to be about 2.210.sup.8 m.sup.2/Vs (negatively charged).

[0059] As illustrated in FIGS. 3, 6 and 7, the microfluidic device can be used to analyze more complicated samples such as proteins. In FIG. 3, 2 mg/ml lysozyme in 10 mM phosphate buffer (pH=7.0) was injected into the separation channel, flanked by 10 mM Phosphate buffer, and 1 M KCl solution was injected into the electrolyte channels (also with 2 mg/ml lysozyme to visualize the interface). Images of intrinsic fluorescence of proteins under ultraviolet light (290 nm) were taken with an UV microscope and a CCD camera. The excitation wavelength is 280 nm [bandwidth 20 nm] and the emission wavelength is 350 nm [Bandwidth 40 nm]. The magnification of the objective is 13X and the camera is a Rolera EMCCD camera with quartz window for UV transmission.

[0060] In addition, FIG. 4a shows an I-V curve of the microfluidic electrophoresis device filled with 1 M KCl in the separation channel and electrolyte channels and FIG. 4b with 1 M KCl in the electrolyte channels and 10 mM KCl in the separation channel. The I-V curve of the microfluidic electrophoresis device was measured with different solutions. The separation channel and the electrolyte channels were firstly filled with 1 M KCl, and then the fluid in the separation channel was changed to 10 mM KCl.

[0061] Assuming that for a microfluidic device filled uniformly with 1 M KCl, the resistance of the separation channel is negligible, the difference of the electric resistance calculated by the two I-V curves is approximately the separation channel resistance (when filled with 10 mM KCl). The result gives a proportion of about 60% of the source voltage dropping on the separation channel. The results are shown in FIG. 3. A good linear relationship can be seen between the current and voltage, and between the sample stream deflection and electric field. The electrophoretic mobility of lysozyme molecules was calculated to be approximately 2.310.sup.8 m.sup.2/Vs.

[0062] In another example, the microfluidic device as disclosed in this invention was also used to study other protein molecules such as Bovine serum albumin (BSA), Beta-lactoglobulin and ovalbumin. Referring to FIG. 6, there is shown the microfluidic electrophoresis of 2 mg/ml Bovine serum albumin in 10 mM phosphate buffer, flanked by 10 mM phosphate buffer, with 1 M KCl electrolyte. Flow rates sample/buffer=20/200 L/h. Referring to FIG. 7, there is shown the microfluidic electrophoresis of 2 mg/ml beta-lactoglobulin in 10 mM phosphate buffer with 1 M KCl electrolyte. Flow rates sample/buffer=10/150 L/h.

[0063] Optionally, a recycling device for controlling a fluid flow is provided and connected to the microfluidic device comprising, the first electrolyte channel with the positive electrode at the downstream outlet of the channel, and the second electrolyte channel with the negative electrode at the downstream outlet of the channel. In particular, the recycling device may be used to control and recycle the high conductivity solution. In one embodiment, the recycling device for controlling a fluid flow may be connected to the microfluidic device as disclosed in this invention and illustrated in FIG. 9.

[0064] Creating a stable interface between the high conductivity solution and the separation medium requires a stable flow between both fluids. Due to the potential requirements of high flow rates of the high conductivity solution, the high conductivity solution may be recycled for practical reasons such as the size of a reservoir, as shown in FIG. 9. Gas and heat may still be effectively kept out of the microfluidic device by using a temperature controlled reservoir and dripping in the used solution to the top of the reservoir, for example. However, dissolved electrolysis products may be difficult to filter out and the ions may have to be replenished.

[0065] As illustrated in FIG. 9, a decoupled, connectable fluidic circuit may be used for the recycling of fluid flows such as the high conductivity solution. The control of fluid flows may require pressure-driven flow, which can be generated by a pressure source 26. Alternatively, the control of fluid flows may use a syringe pump 21. Additionally, the high conductivity solution can be stored in an inlet reservoir 28 and can be pumped into the microfluidic device 30. The inlet reservoir 28 can be closed by a removable seal 32.

[0066] Optionally, the high conductivity solution may be pumped out of the microfluidic device 30, and may be stored in an outlet reservoir 29. As shown in FIG. 9, the inlet side 22 and the outlet side 24 of the connectable fluidic circuit are decoupled during the recycling of fluid flows, but can be bought back into contact after the recycling operation. The device 30 including a recycling loop 31 is configured to reintroduce fluid from the outlet reservoir 29 into the device 30 via a valve 33. The valve 33 is operable to refill the syringe pump 21 after an operation has been completed and prior to the commencement of a subsequent operation. The device as disclosed herein may allow for high-precision flow control in the form of pressure-driven flow or syringe pumps.

[0067] In contrast, a closed circuit necessitates for instance a peristaltic pump which is typically not pulse-free. In addition, a completely open circuit does not allow for automated recycling of fluid flows for example, the high conductivity solution.

[0068] It will further be appreciated by those skilled in the art that although the invention has been described by way of example with reference to several embodiments. It is not limited to the disclosed embodiments and that alternative embodiments could be constructed without departing from the scope of the invention as defined in the appended claims.