Manipulation of fluids, fluid components and reactions in microfluidic systems

US10960397B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10960397-B2
Application numberUS-202016916532-A
CountryUS
Kind codeB2
Filing dateJun 30, 2020
Priority dateApr 19, 2007
Publication dateMar 30, 2021
Grant dateMar 30, 2021

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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.

Microfluidic structures and methods for manipulating fluids, fluid components, and reactions are provided. In one aspect, such structures and methods can allow production of droplets of a precise volume, which can be stored/maintained at precise regions of the device. In another aspect, microfluidic structures and methods described herein are designed for containing and positioning components in an arrangement such that the components can be manipulated and then tracked even after manipulation. For example, cells may be constrained in an arrangement in microfluidic structures described herein to facilitate tracking during their growth and/or after they multiply.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for partitioning a fluid sample, the method comprising: providing a microfluidic device having a substrate comprising a plurality of microwells in fluid communication with an inlet; introducing a first fluid into the inlet of the microfluidic device, the first fluid comprising a biological sample and a plurality of beads, each bead comprising a reactive component for binding a target molecule from the biological sample to the bead; introducing a second fluid immiscible with the first fluid into the microfluidic device and flowing the second fluid towards each of the plurality of microwells so as to form partitions of fluid in corresponding microwells, wherein at least some of the partitions include a subvolume of the first fluid, a portion of the biological sample, and a single bead; and maintaining each partition of fluid in corresponding microwells for detection of contents in at least one partition. 2. The method of claim 1 , further comprising performing an ELISA assay for the detection of the contents in the at least one partition. 3. The method of claim 1 , wherein a subset of the partitions do not include any beads. 4. The method of claim 1 , wherein the second fluid is an oil. 5. The method of claim 1 , further comprising monitoring one or more of the partitions of fluid and detecting, with an optical detector, emissions from one or more detectable labels associated with one or more beads. 6. The method of claim 5 , further comprising determining the presence of the target molecules based on the detection of emissions. 7. The method of claim 5 , further comprising measuring, with the optical detector, an intensity of a signal emitted from at least one of the detectable labels. 8. The method of claim 7 , further comprising capturing one or more images of a signal emitted from at least one of the detectable labels. 9. The method of claim 5 , wherein, upon a reaction in at least one partition of fluid, the emissions are emitted from one or more of the detectable labels. 10. The method of claim 1 , wherein the target molecule is a protein. 11. A method for partitioning a fluid sample, the method comprising: providing a microfluidic device having a substrate comprising a plurality of regions in fluid communication with an inlet; introducing an aqueous fluid into the inlet of the microfluidic device, the aqueous fluid comprising a biological sample and a plurality of beads, each bead comprising a reactive component for binding a target protein molecule from the biological sample to the bead; partitioning the aqueous fluid into a plurality of fluid partitions confined within a plurality of corresponding regions of the substrate by introducing a second fluid immiscible with the aqueous fluid into the microfluidic device and flowing the second fluid towards the plurality of regions, wherein for a subset of the fluid partitions, each fluid partition of the subset comprises a subvolume of the aqueous fluid and one bead; and maintaining each fluid partition of the subset in a corresponding region for detection of contents therein. 12. The method of claim 11 , further comprising performing an ELISA assay for the detection of the contents. 13. The method of claim 11 , wherein the second fluid is an oil. 14. The method of claim 11 , further comprising monitoring one or more of the fluid partitions and detecting, with an optical detector, emissions from one or more detectable labels associated with one or more beads and determining the presence of target protein molecules based on the detection of emissions. 15. A method for partitioning a fluid sample, the method comprising: providing a microfluidic device having a substrate comprising a plurality of microwells in fluid communication with an inlet; introducing an aqueous fluid into the inlet of the microfluidic device, the aqueous fluid comprising a biological sample and a plurality of beads, each bead comprising a reactive component for binding a target molecule from the biological sample to the bead; introducing a second fluid immiscible with the aqueous fluid into the microfluidic device and flowing the second fluid towards each of the plurality of microwells so as to form aqueous partitions in corresponding microwells, wherein at least some of the aqueous partitions include a subvolume of the first fluid, at least a portion of the biological sample, and a single bead; and maintaining each aqueous partition in corresponding microwells for detection of contents of at least one partition. 16. The method of claim 15 , further comprising performing an ELISA assay for the detection of the contents of the at least one partition. 17. The method of claim 15 , wherein a subset of the aqueous partitions do not include any beads.

Assignees

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Classifications

  • Flow chambers · CPC title

  • vents used to stop and induce flow, backpressure valves · CPC title

  • With control of flow by a condition or characteristic of a fluid · CPC title

  • Involving pressure control · CPC title

  • Conveying liquids or viscous products by pressure of another fluid · CPC title

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What does patent US10960397B2 cover?
Microfluidic structures and methods for manipulating fluids, fluid components, and reactions are provided. In one aspect, such structures and methods can allow production of droplets of a precise volume, which can be stored/maintained at precise regions of the device. In another aspect, microfluidic structures and methods described herein are designed for containing and positioning components i…
Who is the assignee on this patent?
Harvard College, Univ Brandeis
What technology area does this patent fall under?
Primary CPC classification B01L3/502784. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Mar 30 2021 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).