Constriction-Expansion Blood Plasma Separation

US2017191982A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2017191982-A1
Application numberUS-201715399285-A
CountryUS
Kind codeA1
Filing dateJan 5, 2017
Priority dateJan 6, 2016
Publication dateJul 6, 2017
Grant date

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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.

A portable, microfluidic blood plasma separation device is presented featuring a constriction-expansion design, which can produce up to about 100% purity for undiluted blood at least about 9% yield. This level of purity represents an improvement of at least one order of magnitude with increased yield compared to that achieved previously using passive separation. The system features high flow rates, 5-30 μL/min plasma collection, with minimal clogging and biofouling. The simple, portable blood plasma separation design can be hand-driven and can easily be incorporated with microfluidic or laboratory scale diagnostic assays. The separation system can be used in conjunction with portable analyte detection tests at concentrations well below clinical relevancy for undiluted whole blood.

First claim

Opening claim text (preview).

1 . A cell separation tool comprising: an inlet channel; an expansion channel in fluid communication with the inlet channel, a width of a proximal end of the expansion channel being approximately equal to a width of the inlet channel, and a width of a distal end of the expansion channel being larger than the width of the inlet channel; at least one side channel in fluid communication with the expansion channel and configured to divert fluid flow from the expansion channel; and an outlet channel in fluid communication with the expansion channel. 2 . The tool of claim 1 , wherein the outlet channel has a width equal to the distal end of the expansion channel. 3 . The tool of claim 1 , wherein the expansion channel has an angle of expansion effective to achieve a cell free layer in the expansion channel proximal to the at least one side channel and, optionally, an angle of expansion effective to produce similar cell separation at a plurality of flow rates. 4 . The tool of claim 1 , wherein the expansion channel has an angle of expansion between about 5 degrees and about 20 degrees, preferably between about 5 and 10 degrees. 5 . The tool of claim 1 , wherein the width of the proximal end of the expansion channel being approximately equal to the width of the inlet channel is a horizontal width, and the width of the distal end of the expansion channel being larger than the width of the inlet channel is a horizontal width. 6 . The tool of claim 1 , wherein the width of the at least one side channel at its point of communication with the expansion channel is less than or equal to the width of the inlet channel. 7 . The tool of claim 1 , wherein each channel is a microchannel. 8 . The tool of claim 1 , wherein the width of the inlet channel is less than about 100 μm, and/or the width of the outlet channel is less than about 200 μm, and/or the width of the at least one side channel is less than about 100 μm. 9 . The tool of claim 1 , wherein the height of the inlet channel, the expansion channel, the at least one side channel and the outlet channel are each, independently, less than about 200 μm. 10 . The tool claim 1 , wherein the expansion channel and each side channel are in fluid communication with a collection reservoir. 11 . The tool of claim 1 , wherein the inlet channel is in fluid communication with an inlet reservoir. 12 . The tool of claim 1 , wherein the inlet channel, the expansion channel, the at least one side channel, and the outlet channel are on a support. 13 . The tool of claim 12 , wherein the support is a glass or silicon wafer. 14 . The tool of claim 1 , wherein the inlet channel is less than about 1 cm in length, and/or the at least one side channels are less than 1 cm. 15 . The tool of claim 1 , wherein the at least one side channel is angled away from the fluid flow. 16 . The tool of claim 1 , wherein the at least one side channel is perpendicular to the fluid flow. 17 . The tool of claim 1 , wherein the at least one side channel is perpendicular to the inlet channel and the outlet channel. 18 . The tool of claim 1 , wherein the tool is configured to cause a horizontal fluid flow and horizontal separation. 19 . The tool of claim 1 , wherein the inlet channel and expansion channel are symmetrical along a central axis and the at least one side channel is perpendicular to the central axis. 20 . The tool of claim 1 , the at least one side channel is located at the junction of the expansion channel and outlet channel. 21 . The tool of claim 1 , wherein at least one side channel is located along each wall of the expansion channel. 22 . The tool of claim 1 , wherein two side channels are located at the junction of the expansion channel and outlet channel. 23 . The tool of claim 1 , wherein the inlet channel has a first fluid flow region and the expansion channel has a second flow region with a different fluid flow pattern than the first fluid flow region. 24 . The tool of claim 1 , wherein the tool is configured to receive fluid pumped by hand. 25 . The tool of claim 1 , wherein the inlet channel is in fluid communication with a fluid inlet port adapted to receive a handheld syringe. 26 . The tool of claim 1 , wherein the at least one side channel is in fluid communication with an analyte test system. 27 . The tool of claim 26 , wherein the analyte test system detects an analyte in blood plasma. 28 . A blood plasma collection tool comprising: an inlet channel; an expansion channel in fluid communication with the inlet channel, a width of the expansion channel expanding from a proximal end of the expansion channel to a distal end of the expansion channel at an angle greater than 0 degrees; at least one side channel in fluid communication with the expansion channel and configured to divert fluid flow from the expansion channel; and an outlet channel in fluid communication with the expansion channel and having a width equal to the distal end of the expansion channel. 29 - 36 . (canceled) 37 . A blood plasma collection tool comprising: an inlet channel; an expansion channel in fluid communication with the inlet channel, a width of a proximal end of the expansion channel being approximately equal to a width of the inlet channel, and a width of a distal end of the expansion channel being larger than the width of the inlet channel; at least one side channel in fluid communication with the expansion channel and configured to divert fluid flow from the expansion channel; and an outlet channel in fluid communication with the expansion channel and having a width equal to the distal end of the expansion channel. 38 . A method of blood plasma collection comprising: pumping blood into an expansion channel having a width expanding from a proximal end of the expansion channel to a distal end of the expansion channel at an angle greater than 0 degrees; and collecting blood plasma from at least one side channel in fluid communication with the expansion channel and configured to divert fluid flow from the expansion channel. 39 - 46 . (canceled) 47 . A method for separating cells from an analyte fluid comprising: a. Providing a tool according to claim 1 ; b. Providing an analyte fluid comprising cells; c. Introducing the fluid into the inlet channel; d. Collecting a cell-free fluid from the at least one side channel; e. Collecting a concentrated fluid comprising cells from the outlet channel. 48 - 60 . (canceled)

Assignees

Inventors

Classifications

  • characterised by bulk separation arrangements on lab-on-a-chip devices, e.g. for filtration or centrifugation · CPC title

  • comprising only one inlet and multiple receiving wells, e.g. for separation, splitting · CPC title

  • Handling flowable solids, e.g. microscopic beads, cells, particles · CPC title

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

  • pistons · CPC title

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What does patent US2017191982A1 cover?
A portable, microfluidic blood plasma separation device is presented featuring a constriction-expansion design, which can produce up to about 100% purity for undiluted blood at least about 9% yield. This level of purity represents an improvement of at least one order of magnitude with increased yield compared to that achieved previously using passive separation. The system features high flow ra…
Who is the assignee on this patent?
Massachusetts Inst Technology
What technology area does this patent fall under?
Primary CPC classification G01N33/491. Mapped technology areas include Physics.
When was this patent published?
Publication date Thu Jul 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).