Devices for separation of particulates, associated methods and systems
Abstract
A device is configured for separation of particulates dispersed within a base fluid, wherein the particulates have a relative density difference compared to the base fluid. The device comprises a microchannel of length l and height h comprising an inlet and an outlet; a microporous surface on one or more walls of the microchannel; a collection chamber on an opposing side of the microporous surface; and an applied force field across the height h of the microchannel to sediment the particles through the microporous surface into the collection chamber. The microporous body operationally generates a fluid flow regime comprising a first fluid flow having a first flow rate through the microchannel and a second fluid flow having a second flow rate through the collection chamber and the second flow rate is a fraction of the first flow rate.
Claims
exact text as granted — not AI-modified1 . A device for separating particulates dispersed within a base fluid and having a relative density difference compared to the base fluid, comprising:
a microchannel of length l and height h disposed between a fluid inlet and a fluid outlet; a microporous body defining at least a portion of the microchannel; and a collection chamber on an opposing side of the microporous body; wherein, the particulates and a portion of the base fluid traverse the microporous body under the influence of an external force field, and are entered and collected in the collection chamber; and wherein the microporous body operationally generates a fluid flow regime comprising a first fluid flow having a first flow rate through the microchannel and a second fluid flow having a second flow rate through the collection chamber and the second flow rate is a fraction of the first flow rate.
2 . The device of claim 1 , wherein the external force field is a gravitational field.
3 . The device of claim 1 , wherein the external force field is an applied force field selected from among an applied magnetic field and an applied electric field.
4 . The device of claim 1 , wherein the microchannel has a length l between about 10 millimeters and about 100 millimeters (mm)
5 . The device of claim 1 , wherein the microchannel has a height h between about 10 micron and about 1000 microns (μm).
6 . The device of claim 1 , wherein the particulates have an average largest dimension between about 1 micron and about 250 microns.
7 . The device of claim 1 , wherein the microporous body comprises pores with an average diameter between about 10 microns and about 500 microns.
8 . The device of claim 1 , wherein the microporous body has porosity between about 10 percent and about 75 percent.
9 . The device of claim 1 , further comprising one or more of a collection chamber fluid inlet and a collection chamber fluid outlet.
10 . The device of claim 1 , further comprising one or more controllers for controlling the applied external force field.
11 . The device of claim 1 , further comprising a fluid driver to induce a flow of particulates dispersed within a base fluid through the microchannel and to drive out a processed fluid enriched in the base fluid and depleted in particulates.
12 . The device of claim 1 , further comprising a fluid driver configured to facilitate recovery of particulates from the collection chamber.
13 . The device of claim 1 , further comprising one or more controllers to control the first fluid flow.
14 . The device of claim 1 , wherein the device is fully automated or partially automated.
15 . The device of claim 1 , wherein one or more of the fluid inlet, the fluid outlet, the microchannel, the microporous body, and the collection chamber is configured to integrate with an analytical device.
16 . The device of claim 1 is configured to separate particulates from one or more of whole blood, petroleum, water, a cell extract, or a tissue extract.
17 . The device of claim 1 is configured to separate particulates from whole blood.
18 . The device of claim 1 is configured to separate red blood cells from whole blood.
19 . The device of claim 1 , wherein the particulates comprise one or more of red blood cells, white blood cells, blood platelets, non-hematic biological cells, tissue fragments, metals, minerals, and non-cellular biological solids.
20 . A device for separating one or more cells dispersed within a base fluid and having a relative density difference compared to the base fluid, the device comprising:
a microchannel of length l and height h disposed between a fluid inlet and a fluid outlet; a microporous body defining at least a portion of the microchannel; and a collection chamber on an opposing side of the microporous body; wherein the cells and a portion of the base fluid traverse the microporous body under the influence of an external force field, and are entered and collected in the collection chamber; and wherein the microporous body operationally generates a fluid flow regime comprising a first fluid flow having a first flow rate through the microchannel and a second fluid flow having a second flow rate through the collection chamber and the second flow rate is a fraction of the first flow rate.
21 . The device of claim 20 , wherein the cells have an average cell diameter (d) between about 1 micron and about 100 microns.
22 . The device of claim 20 , wherein the microchannel has a height h between about 10 microns and about 1000 microns.
23 . The device of claim 20 , wherein the microporous body has an average pore diameter (p) between about 10 microns and about 500 microns.
24 . The device of claim 20 , wherein the microporous body has an average porosity (q) between about 10 percent and about 75 percent.
25 . A method for separating particulates dispersed within a base fluid and having a relative density difference compared to the base fluid, comprising:
providing a separation device comprising:
a microchannel of length l and height h disposed between a fluid inlet and a fluid outlet; a microporous body defining at least a portion of the microchannel; and a collection chamber on an opposing side of the microporous body; wherein the particulates and a portion of the base fluid traverse the microporous body under the influence of an external force field, and are entered and collected in the collection chamber;
introducing a sample of unprocessed fluid comprising particulates dispersed within a base fluid into the microchannel via the fluid inlet; separating at least a portion of the particulates from the unprocessed fluid to provide a stream of processed fluid at the fluid outlet; and recovering at least a portion of the particulates initially present in the unprocessed fluid in the collection chamber; wherein the particulates and a portion of the base fluid traverse the microporous body under the influence of an external force field, and are entered and collected in the collection chamber; and wherein the microporous body operationally generates a fluid flow regime comprising a first fluid flow having a first flow rate through the microchannel and a second fluid flow having a second flow rate through the collection chamber and the second flow rate is a fraction of the first flow rate.
26 . The method of claim 25 , further comprising a step of priming the device prior to introducing the unprocessed fluid into the microchannel.
27 . The method of claim 25 , further comprising re-traversing the fluid through the microporous body and re-entering the microchannel.
28 . The method of claim 25 , wherein the unprocessed fluid is a biological sample.
29 . The method of claim 28 , wherein the unprocessed fluid comprises one or more of whole blood, a cell extract, or a tissue extract.
30 . The method of claim 28 , wherein the unprocessed fluid comprises whole blood.
31 . The method of claim 28 , wherein the particulates are blood cells.
32 . The method of claim 28 , wherein the processed fluid comprises blood plasma.
33 . A method for separating cells dispersed within a base fluid of whole blood sample, comprising:
providing a separation device comprising:
a microchannel of length l and height h disposed between a fluid inlet and a fluid outlet; a microporous body defining at least a portion of the microchannel; and a collection chamber on an opposing side of the microporous body; wherein the particulates and a portion of the base fluid traverse the microporous body under the influence of an external force field, and are entered and collected in the collection chamber;
introducing the whole blood sample of unprocessed fluid comprising cells dispersed within a base fluid into the microchannel via the fluid inlet; separating at least a portion of the cells from the unprocessed fluid to provide a stream of processed fluid at the fluid outlet; and recovering at least a portion of the cells initially present in the unprocessed fluid in the collection chamber; wherein the particulates and a portion of the base fluid traverse the microporous body under the influence of an external force field, and are entered and collected in the collection chamber; and wherein the microporous body operationally generates a fluid flow regime comprising a first fluid flow having a first flow rate through the microchannel and a second fluid flow having a second flow rate through the collection chamber and the second flow rate is a fraction of the first flow rate.
34 . The method of claim 33 , wherein the processed fluid comprises blood plasma which is substantially free of blood cells.
35 . The method of claim 33 , wherein the cells recovered in the collection chamber is substantially free of blood plasma.Join the waitlist — get patent alerts
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