Microfluidic device and method for shear stress-induced transformation of cells
US-10722540-B1 · Jul 28, 2020 · US
US12292046B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12292046-B2 |
| Application number | US-201917058634-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 29, 2019 |
| Priority date | May 30, 2018 |
| Publication date | May 6, 2025 |
| Grant date | May 6, 2025 |
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A microfluidic tissue dissociation and filtration device simultaneously filters large tissue fragments and dissociates smaller aggregates into single cells, thereby improving single cell yield and purity. The device includes an inlet coupled to a first microfluidic channel at an upstream location and a first outlet at a downstream location. A first filter membrane is interposed between the first microfluidic channel and a second microfluidic channel, wherein the second microfluidic channel is in fluidic communication with the first microfluidic channel via the first filter membrane. The first filter membrane operates under a tangential flow format. A second outlet is coupled to a downstream location of the second microfluidic channel and includes a second filter membrane interposed between the second outlet and the second microfluidic channel. The dual membrane device increased single cell numbers by at least 3-fold for different tissue types.
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What is claimed is: 1. A microfluidic tissue dissociation and filtration device comprising: an inlet coupled to a first microfluidic channel at an upstream location, the first microfluidic channel coupled to a first outlet at a downstream location, wherein the first microfluidic channel is disposed in a first layer of the microfluidic tissue dissociation and filtration device; a second microfluidic channel located within a second layer of the microfluidic tissue dissociation and filtration device; a first filter membrane interposed between the first microfluidic channel and the second microfluidic channel, wherein the second microfluidic channel is in fluidic communication with the first microfluidic channel by a first connecting fluid passageway containing the first filter membrane; a second outlet coupled to a downstream location of the second microfluidic channel; a second filter membrane interposed between the second outlet and the second microfluidic channel and contained in a second connecting fluid passageway that fluidically connects the second microfluidic channel to the second outlet; a pump connected to a source of tissue or cellular aggregates contained within a fluid, the pump further fluidically connected to the inlet; and wherein the first filter membrane comprises pores having diameters of d 1 and wherein the second filter membrane comprises pores having diameters of d 2 , wherein d 1 >d 2 and wherein the first filter membrane has pore diameters that are at least two times the pore diameters of the second filter membrane, and wherein the second filter membrane is configured to allow passage of single cells and fluid and generates an increase in yield of single cells from the tissue or cell aggregates of at least 3-fold in the second outlet. 2. The microfluidic tissue dissociation and filtration device of claim 1 , wherein the first filter membrane has pore diameters greater than 15 μm and less than 1,000 μm and the second filter membrane has pore diameters greater than 5 μm and less than or equal to 100 μm. 3. The microfluidic tissue dissociation and filtration device of claim 2 , wherein the first connecting fluid passageway is formed in a third or more additional layers. 4. The microfluidic tissue dissociation and filtration device of claim 1 , wherein the first filter membrane and the second filter membrane comprise a single layer of woven mesh polymer thread. 5. The microfluidic tissue dissociation and filtration device of claim 4 , wherein the first filter membrane and the second filter membrane are formed from a polyamide thread. 6. The microfluidic tissue dissociation and filtration device of claim 1 , wherein the first connecting fluid passageway comprises a via, hole, or aperture that extends between the first microfluidic channel and the second microfluidic channel. 7. The microfluidic tissue dissociation and filtration device of claim 1 , wherein the second connecting fluid passageway comprises a via, hole, or aperture that extends between the second microfluidic channel and the second outlet. 8. The microfluidic tissue dissociation and filtration device of claim 1 , wherein the first filter membrane and the second filter membrane respectively comprise a single layer of woven mesh that is interposed between the first and second layers of the microfluidic tissue dissociation and filtration device. 9. The microfluidic tissue dissociation and filtration device of claim 1 , wherein the pore diameters of the second filter membrane are between 10-20 μm and the first filter membrane has pore diameters that are between 2-3 times larger than the pore diameters of the second filter membrane. 10. The microfluidic tissue dissociation and filtration device of claim 1 , wherein the second filter membrane generates an increase in yield of single cells from the tissue or cell aggregates of at least 10-fold in the second outlet.
by mechanical forces; Stirring; Trituration; Comminuting (crushing, pulverizing, disintegrating in general B02C) · CPC title
Cell isolation or sorting (purging biological preparations of unwanted cells C12N5/0081, determining the presence or kind of microorganism C12Q1/04) · CPC title
Pore size · CPC title
comprising only one inlet and multiple receiving wells, e.g. for separation, splitting · CPC title
Cards, e.g. flat sample carriers usually with flow in two horizontal directions · CPC title
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