Microfluidic trap
Provided herein are microfluidic devices that can be configured to generate an electrophoretic flow that is in opposition to a fluid flow through a microcapillary of a microfluidic device provided herein. Also provided herein are methods that include adding an amount of particle to the inlet area of the microfluidic device as provided herein, generating a first fluid flow through the microcapillary of the microfluidic device provided herein; and applying a uniform electric field to the microfluidic device, where the uniform electric field generates an electrophoretic flow that is in opposition to the fluid flow.
1 . A method comprising:
adding particles to a microfluidic device, wherein the microfluidic device comprises an inlet area, wherein the inlet area has an entry region, and wherein the particles are added to the inlet area;
an outlet area, where the outlet area has an exit region; and
a single microcapillary, wherein the single microcapillary is fluidly coupled to the entry region of the inlet area and the exit region of the outlet area;
generating a first fluid flow through the single microcapillary of the microfluidic device with a first fluid flow generator; and
applying a uniform electric field to the microfluidic device, where the uniform electric field generates an electrophoretic flow that is in opposition to the first fluid flow;
tuning the uniform electric field, the first fluid flow, or the uniform electric field and the first fluid flow, such that a plurality of the particles present in the single microcapillary migrate to a wall of the single microcapillary and subsequently migrate against the first fluid flow to a stagnation point at the entry region of the inlet area.
2 . The method of claim 1 , further comprising concentrating the plurality of the particles at the stagnation point.
3 . The method of claim 1 , wherein the particles are charged particles.
4 . The method of claim 2 , further comprising the step of quantitating the amount of the plurality of particles concentrated at the stagnation point.
5 . The method of claim 2 , further comprising the step of collecting the plurality of particles concentrated at the stagnation point.
6 . The method of claim 5 , collecting is performed by applying a second fluid flow to the stagnation point that is not parallel to the first fluid flow.
7 . The method of claim 6 , wherein the second fluid flow is about perpendicular to the first fluid flow.
8 . The method of claim 1 , wherein the plurality of particles comprises at least DNA, and further comprising the step of separating the DNA from at least one other particle of the plurality of particles via tuning the uniform electric field, the first fluid flow, or the uniform electric field and the first fluid flow.
9 . The method of claim 1 , wherein the single microcapillary further comprises a neutral coating on one or more walls of the single microcapillary.
10 . The method of claim 1 , wherein tuning the uniform electric field, the first fluid flow, or the uniform electric field and the first fluid flow, such that the plurality of the particles present in the single microcapillary migrate to a wall of the single microcapillary and subsequently migrate against the first fluid flow to the stagnation point comprises altering the magnitude and relative direction of the first fluid flow and electric field to trap particles along the wall.
11 . The method of claim 1 , wherein applying the uniform electric field to the microfluidic device comprises applying an axial electric field to the fluid.
12 . The method of claim 1 , wherein the microfluidic device has one or more step-changes in cross-sectional area in one or more areas across a length of the device.
13 . The method of claim 1 , wherein the first fluid flow generator is configured to generate a fluid flow through the single microcapillary at a flow velocity of 0 μm/s to 3000 μm/s.
14 . The method of claim 1 , wherein the inlet area, the outlet area, and the single microcapillary are formed from a single structure using laser etching.
15 . A method comprising:
adding particles to a microfluidic device, wherein the microfluidic device comprises an inlet area, wherein the inlet area has an entry region, wherein the particles are added to the inlet area;
an outlet area, where the outlet area has an exit region; and
a single microcapillary coated with a charge-neutral compound or charge-neutral polymer, wherein the single microcapillary is fluidly coupled to the entry region of the inlet area and the exit region of the outlet area, wherein the inlet area, the outlet area, and the single microcapillary are formed from a single structure using laser etching, and wherein the microfluidic device has one or more step-changes in cross-sectional area in one or more areas across a length of the device;
generating a fluid flow through the single microcapillary of the microfluidic device with a fluid flow generator; and
applying a uniform electric field to the microfluidic device, where the uniform electric field generates an electrophoretic flow that is in opposition to the fluid flow;
tuning the uniform electric field, the fluid flow, or the uniform electric field and the fluid flow, such that a plurality of the particles present in the single microcapillary migrate to a wall of the single microcapillary and subsequently migrate against the fluid flow to a stagnation point, wherein the stagnation point is located at the entry region of the inlet area.
16 . The method of claim 15 , further comprising concentrating the plurality of the particles at the stagnation point.
17 . The method of claim 16 , further comprising the step of quantitating the amount of the plurality of particles concentrated at the stagnation point.
18 . The method of claim 16 , further comprising the step of collecting the plurality of particles concentrated at the stagnation point.
19 . The method of claim 15 , wherein tuning the uniform electric field, the fluid flow, or the uniform electric field and the fluid flow, such that the plurality of the particles present in the single microcapillary migrate to a wall of the single microcapillary and subsequently migrate against the fluid flow to the stagnation point comprises altering the magnitude and relative direction of the fluid flow and electric field to trap particles along the wall.
20 . A method comprising:
adding particles to a microfluidic device, wherein the microfluidic device consists of
an inlet area having an entry region;
an outlet area having an exit region;
a single microcapillary coated with a charge-neutral compound or charge-neutral polymer, where the microcapillary is fluidly coupled to the entry region of the inlet area and the exit region of the outlet area, and wherein the inlet area, the outlet area, and the single microcapillary are formed from a single structure using laser etching;
a fluid flow generator configured to generate a fluid flow through the microcapillary;
an electric current generator configured to generate an electrophoretic flow through the microcapillary, where the electrophoretic flow is in opposition to the fluid flow, and where the electrophoretic flow is tuned to the fluid flow such that one or more types of particles present in the microcapillary migrate to a wall of the microcapillary
and subsequently migrate against the fluid flow to a stagnation region, and wherein the microfluidic device has one or more step-changes in cross-sectional area in one or more areas across a length of the device;
generating a fluid flow through the microcapillary of the microfluidic device with the fluid flow generator; and
applying a uniform electric field to the microfluidic device with the electric current generator, where the uniform electric field generates an electrophoretic flow that is in opposition to the fluid flow;
tuning the uniform electric field, the fluid flow, or the uniform electric field and the fluid flow, such that one or more of the particles present in the microcapillary migrate to a wall of the microcapillary and subsequently migrate against the fluid flow to a stagnation point in the microcapillary.