Devices and methods for quantification of male fertility
US-2018348207-A1 · Dec 6, 2018 · US
US2023242872A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2023242872-A1 |
| Application number | US-202318114022-A |
| Country | US |
| Kind code | A1 |
| Filing date | Feb 24, 2023 |
| Priority date | Jan 22, 2016 |
| Publication date | Aug 3, 2023 |
| Grant date | — |
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A microfluidic chip is provided for self-sorting highly motile, morphologically normal sperm cell with high DNA integrity from a fresh semen sample. The sperm self-sorting microfluidic chip has one or more inlet chambers, and sperm collection outlet chamber(s), and the middle of the channel features various micro-fabricated structures in different geometrical shapes and orientations, with varying periodicities and patterns, such as an array of micro-fabricated pillars that facilitate the transport of the active and healthy sperm into the outlet chamber.
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We claim: 1 . A device for self-sorting motile, morphologically-normal sperm cells with high DNA integrity from raw or unprocessed semen, comprising: a fluidic channel with an inlet at one end and an outlet at the other end, wherein an array of pillar-structures is periodically spaced inside the fluidic channel, wherein the spacing between adjacent pillar-structures ranges from one micrometer to 250 micrometers, wherein the inlet is used for induction of the raw or unprocessed semen to the fluidic channel, wherein the outlet is used for collection of sorted sperm cells from the fluidic channel, wherein the sorted sperm cells have been self-sorted by their own self-induced movements within the fluidic channel through their interactions with the periodically spaced array of pillar-structures, wherein the device and the self-sorting operates without the use of any external flow, forces or mechanisms to feed the raw or unprocessed semen through the fluidic channel, and wherein the self-sorting outputs in the outlet the motile, morphologically-normal sperm cells with high DNA integrity compared to the raw or unprocessed semen. 2 . The device of claim 1 , wherein a length of the fluidic channel ranges from 4 mm to 20 mm, and wherein a height of the pillar-structures ranges from 20 μm to 80 μm. 3 . The device of claim 1 , wherein the spacing between adjacent pillar-structures ranges from 5 μm to 200 μm. 4 . The device of claim 1 , wherein the spacing between adjacent pillar-structures ranges from 5 μm to 30 μm. 5 . The device of claim 1 , wherein the spacing between adjacent pillar-structures ranges from 18 μm to 30 μm. 6 . The method of claim 1 , wherein the length of the fluidic channel ranges from 12 mm to 20 mm. 7 . The device of claim 1 , wherein the width of the fluidic channel is 1.5 mm. 8 . The device of claim 1 , wherein the array of pillar-structures has a periodicity of 18×26 μm, 22×22 μm, 22×26 μm, 26×26 μm or 30×26 μm. 9 . The device of claim 1 , wherein the spacing between adjacent pillar-structures ranges from 18 μm to 30 μm in a first direction. 10 . The device of claim 9 , wherein the spacing between the adjacent pillar-structures ranges from 22 μm to 26 μm in a second direction.
sorting of gametes, e.g. according to sex or motility · CPC title
characterised by the means for controlling flow resistance, e.g. flow controllers, baffles or throttle valves · CPC title
specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads or physically stretching molecules · 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
Sperm cells, spermatogonia · CPC title
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