Liquid Biopsy Detection of Leukemia Using Closed-Loop Microfluidics
US-2018136210-A1 · May 17, 2018 · US
US11833508B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11833508-B2 |
| Application number | US-202117488463-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 29, 2021 |
| Priority date | Nov 15, 2018 |
| Publication date | Dec 5, 2023 |
| Grant date | Dec 5, 2023 |
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Described is a multi-dimensional double spiral (MDDS) microfluidic device comprising a first spiral microchannel and a second microchannel, wherein the wherein the first spiral microchannel and second spiral microchannel have different cross-sectional areas. Also described is a device comprising a multi-dimensional double spiral and system for recirculation. The invention also encompasses methods of separating particles from a sample fluid comprising a mixture of particles comprising the use of the multi-dimensional double spiral microfluidic device.
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What is claimed is: 1. A method of separating sperm cells from a sample fluid comprising a mixture of sperm and cells, wherein the sample fluid is a semen sample, the method comprising the steps of: a. introducing a sample fluid comprising sperm and cells into a first inlet of a first spiral microchannel of a microfluidic device comprising a multidimensional double spiral (MDDS), wherein the MDDS comprises: i. the first spiral microchannel comprising the first inlet and a first outlet; ii. a second spiral microchannel in fluid communication with the first spiral microchannel and comprising an inner wall outlet and an outer wall outlet, wherein the inner wall outlet is located on the inner wall side of the second spiral microchannel and the outer wall outlet is located on the outer wall side of the second microchannel; and iii. a transition region, wherein the transition region is a microchannel that connects the first and the second spiral microchannels, wherein a first end of the transition region microchannel has the same diameter as the first spiral microchannel and is connected to the outlet of the first spiral microchannel and a second end of the transition region microchannel has the same diameter as the second spiral microchannel and is connected to the inlet of the second spiral microchannel, wherein the output from the first spiral microchannel is directed into the second spiral microchannel in through the transition region microchannel; wherein the first spiral microchannel has a smaller cross-sectional area than the second spiral microchannel; wherein the cross-sectional area of the first spiral microchannel remains constant along the length of the first spiral microchannel and wherein the cross-sectional area of the second spiral microchannel remain constant along its length; and wherein the MDDS is configured to separate cells and sperm from a sample fluid comprising a mixture of sperm and cells; b. directing the sample fluid through the first spiral microchannel to the transition region microchannel of the microfluidic device and into the second spiral microchannel, and c. directing a first stream comprising cells to the inner wall outlet and directing a second stream comprising sperm to the outer wall outlet, wherein the first spiral microchannel concentrates the cells and sperm into a concentrated cell and sperm stream and the second spiral microchannel separates sperm from the cells in the concentrated cell and sperm stream based on their sizes. 2. The method of claim 1 , further comprising collecting the second sperm stream from the outer wall outlet. 3. The method of claim 1 , wherein the first inlet is the only inlet of the microfluidic device. 4. The method of claim 1 , wherein the first spiral microchannel forms the concentrated cell stream on the inner wall side of the first spiral microchannel. 5. The method of claim 1 , wherein the concentrated sperm stream enters the outer wall side of the second spiral microchannel. 6. The method of claim 5 , wherein the second spiral microchannel directs a first cell stream to the inner wall outlet and directs a second sperm stream to the outer wall outlet, wherein the first cell stream comprises cells having a larger average diameter than that of the sperm in the second sperm stream. 7. The method of claim 1 , wherein the method separates sperm from cells in the semen sample and concentrates the sperm. 8. The method of claim 1 , wherein the first spiral microchannel is configured to concentrate the cells and sperm into a concentrated stream and the second spiral microchannel is configured to separate sperm from the cells based on the sizes of the sperm and the cells; wherein the microfluidic device is configured to provide closed loop recirculation of the sample fluid through the first spiral microchannel; wherein the inner wall outlet of the MDDS is in fluid communication with a first output reservoir and the outer wall outlet is in fluid communication with a second output reservoir; and wherein the system for closed loop recirculation recirculates the sample fluid from the second output reservoir into the inlet of the first spiral channel, and comprises a syringe in fluid communication with the second output reservoir and the inlet of the first spiral channel; a first check valve positioned between and in fluid communication with the second output reservoir and the syringe, wherein the first check valve blocks flow from the syringe to the second output reservoir when the syringe is actuated to infuse the sample fluid into the inlet of the first spiral channel; and a second check valve positioned between and in fluid communication with the syringe and the inlet of the first spiral channel, wherein the second check valve blocks flow from the inlet of the first spiral channel to the syringe when the syringe is actuated to withdraw the sample fluid from the second output reservoir into the syringe; and wherein the system for closed loop recirculation recirculates the sample fluid from the first output reservoir into the first inlet of the first microchannel; wherein the inner wall outlet directs the first cell stream to the first output reservoir and the outer wall outlet directs the second sperm stream to the second output reservoir, wherein the sample fluid in the second output reservoir is recirculated by actuating the syringe to withdraw the sample fluid from the second output reservoir and infuse the sample fluid into the first inlet of the first spiral microchannel. 9. The method of claim 8 , comprising at least two cycles of recirculation. 10. The method of claim 1 , wherein the microfluidic device comprises at least two multi-dimensional double spirals, wherein the first inlet of each of the microfluidic devices is in fluid communication with the sample fluid. 11. The method of claim 10 , wherein the microfluidic device comprises four multi-dimensional double spirals. 12. The method of claim 1 , wherein the second spiral microchannel is nested within the first microchannel. 13. The method of claim 1 , wherein the first inlet is on the circumference of the first spiral microchannel. 14. The method of claim 1 , wherein the outlets of the second spiral microchannel are on the circumference of the second spiral microchannel. 15. The method of claim 1 , wherein the transition region is on the interior of the nested spiral microchannels. 16. The method of claim 1 , wherein the transition region is S-shaped. 17. The method of claim 1 , wherein the second microchannel has a non-rectangular cross-section and wherein the first spiral microchannel has a rectangular cross-section. 18. The method of claim 17 , wherein the second microchannel has a trapezoidal cross section defined by a radially inner side, a radially outer side, a bottom side, and a top side, the cross section having a) the radially inner side and the radially outer side unequal in height, or b) the radially inner side equal in height to the radially outer side, and wherein the top side has at least two continuous straight sections, each unequal in width to the bottom side. 19. The method of claim 18 , wherein the second microchannel cross sections has (a) the height of the radially inner side larger than the height of the radially outer side, or (b) the height of the radially inner side is smaller than the height of the radially outer side, or (c) the top side includes at least one step forming a stepped profile, or (d) the top side includes at least one shallow region in between the radially inner
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 · CPC title
Sorting or classification of particles or molecules · CPC title
rectangular shaped · CPC title
comprising only one inlet and multiple receiving wells, e.g. for separation, splitting · CPC title
Serpentine channels · CPC title
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