Fluidic devices, systems, and methods for encapsulating and partitioning reagents, and applications of same

US10071377B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10071377-B2
Application numberUS-201715687856-A
CountryUS
Kind codeB2
Filing dateAug 28, 2017
Priority dateApr 10, 2014
Publication dateSep 11, 2018
Grant dateSep 11, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The disclosure provides devices, systems and methods for the generation of encapsulated reagents and the partitioning of encapsulated reagents for use in subsequent analyses and/or processing, such as in the field of biological analyzes and characterization.

First claim

Opening claim text (preview).

What is claimed is: 1. A microfluidic system, comprising: a first fluid source fluidly connected to a first channel and comprising a first fluid that comprises an aqueous fluid and a plurality of microcapsules; a second fluid source fluidly connected to a second channel and comprising a second fluid that is immiscible with the aqueous fluid; a droplet generation junction fluidly connected to a third channel; a flow regulator fluidly connected to the first channel and a fourth channel, wherein the flow regulator (1) accepts microcapsules from the plurality of microcapsules from the first channel and (2) provides the microcapsules in the fourth channel, wherein the flow regulator has a cross-section that is greater than a cross-section of the first channel such that the microcapsules flow at a flow frequency that is substantially regular in the fourth channel as determined by a number of microcapsules that flow past a given point in the fourth channel within a one second period of time; a flow control system that: (i) subjects the first fluid from the first fluid source to flow along the first channel, through the flow regulator, and into the fourth channel, such that the microcapsules from the plurality of microcapsules flow at the flow frequency that is substantially regular in the fourth channel as determined by the number of microcapsules that flow past the given point in the fourth channel within the one second period of time, and (ii) subjects the second fluid from the second fluid source to flow along the second channel, such that the microcapsules and the second fluid meet at the droplet generation junction to generate a plurality of droplets comprising the microcapsules from the plurality of microcapsules, which plurality of droplets flow along the third channel. 2. The microfluidic system of claim 1 , wherein the flow frequency has a coefficient of variation of less than 30%. 3. The microfluidic system of claim 2 , wherein the flow frequency has a coefficient of variation of less than 20%. 4. The microfluidic system of claim 3 , wherein the flow frequency has a coefficient of variation of less than 10%. 5. The microfluidic system of claim 4 , wherein the flow frequency has a coefficient of variation of less than 5%. 6. The microfluidic system of claim 1 , wherein the flow frequency is greater than 50 Hz. 7. The microfluidic system of claim 6 , wherein the flow frequency is greater than 500 Hz. 8. The microfluidic system of claim 7 , wherein the flow frequency is greater than 1000 Hz. 9. The microfluidic system of claim 8 , wherein the flow frequency is greater than 2000 Hz. 10. The microfluidic system of claim 9 , wherein the flow frequency is greater than 5000 Hz. 11. The microfluidic system of claim 1 , wherein the flow frequency provides the microcapsules in the plurality of droplets at an occupancy of no more than 1 microcapsule per droplet. 12. The microfluidic system of claim 1 , wherein the flow frequency in the fourth channel is relative to an upstream irregular flow of microcapsules from the plurality of microcapsules in the first channel. 13. The microfluidic system of claim 1 , wherein the aqueous fluid comprises a biological molecule. 14. The microfluidic system of claim 1 , wherein the plurality of microcapsules comprises reagents. 15. The microfluidic system of claim 14 , wherein the reagents are encapsulated in the plurality of microcapsules. 16. The microfluidic system of claim 14 , wherein the reagents are barcode sequences. 17. The microfluidic system of claim 1 , wherein the plurality of microcapsules is monodisperse. 18. The microfluidic system of claim 17 , wherein microcapsules of the plurality of microcapsules have a mean cross-sectional dimension and a coefficient of variation in cross-sectional dimension of no greater than 30%. 19. The microfluidic system of claim 18 , wherein microcapsules of the plurality of microcapsules have a mean cross-sectional dimension and a coefficient of variation in cross-sectional dimension of no greater than 10%. 20. The microfluidic system of claim 1 , wherein the flow control system comprises a funneling structure. 21. The microfluidic system of claim 1 , wherein the flow control system subjects the microcapsules and second fluid to flow into the droplet generation junction at flow rates that are selected to generate the plurality of droplets such that a given droplet of the plurality of droplets comprises a single microcapsule form the plurality of microcapsules. 22. The microfluidic system of claim 1 , further comprising a third fluid source fluidly connected to the fourth channel through a fifth channel, wherein the third fluid source comprises a third fluid comprising an additional aqueous fluid. 23. The microfluidic system of claim 22 , wherein the first channel and the fifth channel meet at an additional junction upstream of the droplet generation junction, wherein the flow control system subjects the third fluid from the third fluid source to flow along the fifth channel to the additional junction, thereby bringing the first fluid and the third fluid in contact to form a mixture comprising the aqueous fluid from the first fluid source and the additional aqueous fluid from the third fluid source. 24. The microfluidic system of claim 1 , wherein microcapsules of the plurality of microcapsules are solid particles. 25. The microfluidic system of claim 1 , wherein microcapsules of the plurality of microcapsules are gel particles. 26. The microfluidic system of claim 1 , wherein the cross section of the flow regulator, along a direction of flow, (i) increases from a first cross-section of the first channel to a second cross-section that is greater than the first cross-section, and (ii) decreases from the second cross-section to a third cross-section of the fourth channel that is less than the second cross-section, which first cross-section, second cross-section and third cross-section are dimensioned such that the microcapsules flow at the flow frequency that is substantially regular in the fourth channel as determined by the number of microcapsules that flow past the given point in the fourth channel within the one second period of time. 27. A microfluidic system, comprising: a first fluid source fluidly connected to a first channel and comprising a first fluid that comprises an aqueous fluid and a plurality of microcapsules; a second fluid source fluidly connected to a second channel and comprising a second fluid that is immiscible with the aqueous fluid; a droplet generation junction fluidly connected to a third channel; a flow regulator fluidly connected to the first channel and a fourth channel, wherein the flow regulator (1) accepts microcapsules from the plurality of microcapsules from the first channel and (2) provides the microcapsules in the fourth channel, wherein the flow regulator has a cross-section that is greater than a cross-section of the first channel such that the microcapsules flow at a flow frequency greater than 50 Hz at a coefficient of variation of less than 30% in the fourth channel as determined by a number of microcapsules that flow past a given point in the fourth channel within a one second period of time; and a flow control system that: (i) subjects the first fluid from the first fluid source to flow along the first channel, through the flow regulator, and into the fourth channe

Assignees

Inventors

Classifications

  • Transferring microquantities of liquid · CPC title

  • Cards, e.g. flat sample carriers usually with flow in two horizontal directions · CPC title

  • using baffles or other fixed flow obstructions · CPC title

  • vacuum · CPC title

  • Handling microquantities of analyte, e.g. microvalves, capillary networks · CPC title

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Frequently asked questions

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What does patent US10071377B2 cover?
The disclosure provides devices, systems and methods for the generation of encapsulated reagents and the partitioning of encapsulated reagents for use in subsequent analyses and/or processing, such as in the field of biological analyzes and characterization.
Who is the assignee on this patent?
10X Genomics Inc
What technology area does this patent fall under?
Primary CPC classification B01L3/0241. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Sep 11 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).