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| 국가/구분 | United States(US) Patent 등록 |
|---|---|
| 국제특허분류(IPC7판) |
|
| 출원번호 | US-0702648 (2010-02-09) |
| 등록번호 | US-8679831 (2014-03-25) |
| 발명자 / 주소 |
|
| 출원인 / 주소 |
|
| 대리인 / 주소 |
|
| 인용정보 | 피인용 횟수 : 30 인용 특허 : 554 |
A microfluidic device includes an input port for inputting a particle-containing liquidic samples into the device, a retention member, and a pressure actuator. The retention member is in communication with the input port and is configured to spatially separate particles of the particle-containing li
A microfluidic device includes an input port for inputting a particle-containing liquidic samples into the device, a retention member, and a pressure actuator. The retention member is in communication with the input port and is configured to spatially separate particles of the particle-containing liquidic sample from a first portion of the liquid of the particle containing fluidic sample. The pressure actuator recombines at least some of the separated particles with a subset of the first portion of the liquid separated from the particles. The device can also include a lysing chamber that receives the particles and liquid from the retention member. The lysing chamber thermally lyses the particles to release contents thereof.
1. A method for processing a particle-containing liquidic sample, comprising: inputting a particle-containing liquidic sample into a microfluidic network of a microfluidic device comprising a retention member comprising an interior surface and an exterior surface, said interior surface being configu
1. A method for processing a particle-containing liquidic sample, comprising: inputting a particle-containing liquidic sample into a microfluidic network of a microfluidic device comprising a retention member comprising an interior surface and an exterior surface, said interior surface being configured to retain particles within an enrichment region of the microfluidic network, and said exterior surface being exterior to the microfluidic network;spatially separating a first portion of the liquid of the particle-containing liquidic sample from particles of the liquidic sample by passing the first portion of the liquid through at least the surface of the retention member wherein the particles are retained in the enrichment region and the first portion of the liquid passes through the exterior surface of the retention member into a reservoir, thereby being expelled from the microfluidic network;passing at least a subset of the expelled first portion from the reservoir through the interior of the retention member back into the microfluidic network, thereby recombining the retained particles with the subset of the first portion of the liquid within the enrichment region; andwherein recombining the retained particles includes reducing a pressure within the microfluidic device by generating a vacuum downstream of the retention member, and wherein generating the vacuum comprises: heating a vacuum chamber downstream of the retention member, wherein a gas is expanded in the vacuum chamber upon heating;expelling at least a portion of the expanded gas from the microfluidic device; andcooling the chamber, wherein the remaining gas is contracted creating a vacuum. 2. A method for processing a sample, comprising: introducing a particle-containing liquidic sample to a microfluidic network of a microfluidic device, wherein the introduction generates a gas pressure within a reservoir in communication with but exterior to the microfluidic network;the reservoir receiving at least some of a first liquidic portion of the particle-containing liquidic sample, and wherein the particles are retained within the microfluidic network;maintaining the pressure within the reservoir; and thenreducing the gas pressure within the reservoir to move a subset of the first liquidic portion from the reservoir back into the microfluidic network, wherein reducing the gas pressure comprises heating a temperature responsive substance to open a channel within the microfluidic network wherein the subset of the first liquidic portion can move. 3. The method of claim 1, wherein generating the vacuum further comprises opening a gate in the microfluidic device between the retention member and the vacuum chamber. 4. The method of claim 1, wherein when the first portion of the liquid passes through the surface of the retention member, it enters a reservoir in communication with the retention member. 5. The method of claim 1, wherein a ratio of a volume of the subset of the first liquidic portion to a volume of the first liquidic portion is at least 1%. 6. The method of claim 1, wherein a ratio of a volume of the subset of the first liquidic portion to a volume of the first liquidic portion is less than 25%. 7. The method of claim 1, wherein the retention member is a filter. 8. The method of claim 1, wherein the particles are DNA. 9. The method of claim 1, wherein the particles are RNA. 10. The method of claim 1, wherein the inputting comprises mating a syringe to an input port of the microfluidic network. 11. The method of claim 10, wherein the inputting step comprises the step of applying pressure to expel the first portion of the liquid from the microfluidic network into the reservoir. 12. The method of claim 2, wherein the introducing includes mating a syringe to an input port of the microfluidic network. 13. The method of claim 12, wherein the introducing step comprises the step of applying pressure to expel the first portion of the liquid from the microfluidic network into the reservoir. 14. The method of claim 2, wherein when the first portion of the liquid is received in the reservoir, the first portion of the liquid passes through a retention member in the microfluidic network. 15. The method of claim 14, wherein the retention member is a filter. 16. The method of claim 2, wherein a ratio of a volume of the subset of the first liquidic portion to a volume of the first liquidic portion is at least 1%. 17. The method of claim 2, wherein a ratio of a volume of the subset of the first liquidic portion to a volume of the first liquidic portion is less than 25%. 18. The method of claim 2, wherein the particles are DNA. 19. The method of claim 2, wherein the particles are RNA.
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