US2016236195A1PendingUtilityA1
Microfluidic particle-analysis systems
Est. expiryJun 27, 2020(expired)· nominal 20-yr term from priority
Inventors:Antoine Daridon
B01L 3/502761C12M 1/34B01L 2400/0655B01L 2200/10B01L 2200/0668B01L 2300/088B01L 2400/0409C12M 23/16B01L 2300/0893G01N 33/4833B01L 2200/0652B01L 2300/0861G01N 15/1484B01L 2300/0887B01L 2300/0645B01L 2300/087B01L 2300/0636G01N 2015/1493B01L 2300/0681B01L 2200/12B01L 2200/0636C12M 21/06B01L 2300/0867B01L 2200/0647G01N 2015/0288G02B 21/32B01L 2400/0415B01L 3/502746B01L 2300/123B01L 2400/0481B01L 2200/16B01L 3/502738B01L 2400/0622B01L 3/502753B01L 2300/06G01N 2015/016G01N 15/149
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Claims
Abstract
The invention provides systems, including apparatus, methods, and kits, for the micro fluidic manipulation and/or detection of particles, such as cells and/or beads. The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and/or analysis of particles, such as cells, viruses, organelles, beads, and/or vesicles. The invention also provides micro fluidic mechanisms for carrying out these manipulations and analyses.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A microfluidic system for cell manipulation comprising:
(a) an input mechanism for introducing a fluid sample containing particles, wherein the particles are beads or cells; (b) a microfluidic passage in fluid communication with said input mechanism; (c) an optical positioning mechanism for positioning said particles in said microfluidic passage while contained in said fluid sample; (d) electrodes suitable for generating and/or regulating movement of the particles; and (e) an optical detection system for analyzing the particles.
2 . The microfluidic system of claim 1 , wherein the particles are cells.
3 . The microfluidic system of claim 2 , wherein the cells are eukaryotic cells.
4 . The microfluidic system of claim 1 , wherein the microfluidic passage has a minimum dimension of less than 200 micrometers.
5 . The microfluidic system of claim 4 , wherein the microfluidic passage has a minimum dimension of less than 100 micrometers.
6 . The microfluidic system of claim 5 , wherein the microfluidic passage has a minimum dimension of less than 50 micrometers.
7 . The microfluidic system of claim 1 , wherein the optical positioning mechanism comprises optical tweezers.
8 . The microfluidic system of claim 7 , wherein the optical tweezers comprise a movable light source for imparting a positioning force on the particles.
9 . The microfluidic device of claim 1 , wherein the optical detection system comprises a light source.
10 . The microfluidic device of claim 9 , wherein the light source is a laser.
11 . The microfluidic device of claim 9 , wherein the light source is a light-emitting diode (LED).
12 . The microfluidic device of claim 1 , wherein the optical detection system comprises a microscope.
13 . The microfluidic device of claim 12 , wherein the microscope is an inverted fluorescence microscope.
14 . The microfluidic device of claim 13 , wherein the microscope is configured to observe individual cells.
15 . The microfluidic device of claim 1 , further comprising a retention mechanism for retaining a particle upon being positioned by said positioning mechanism.
16 . The microfluidic device of claim 15 , wherein the retention mechanism is configured to retain a single cell.
17 . The microfluidic device of claim 15 , wherein the retention mechanism comprises a physical barrier.
18 . The microfluidic device of claim 16 , further comprising a release mechanism for releasing the cell from said retention mechanism.
19 . The microfluidic device of claim 18 , wherein the release mechanism is for rendering ineffective the retention mechanism by lysing said cell to release intracellular components.
20 . The microfluidic device of claim 1 , further comprising a treatment mechanism for exposing the particles to a reagent.Join the waitlist — get patent alerts
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