Microfluidic device possessing structures enabling differential analysis of a single cell's constituents

Patent metadata

Field	Value
Publication number	US-2020246798-A1
Application number	US-201615776221-A
Country	US
Kind code	A1
Filing date	Nov 15, 2016
Priority date	Nov 20, 2015
Publication date	Aug 6, 2020
Grant date	—

Abstract

A method and a micro fluidic device comprising at least one micro fluidic structure for differential extraction of nuclear and extra-nuclear constituents of a single cell, said micro fluidic structure comprising a feeding channel for receiving a volume of a sample containing at least one cell, at least one trapping structure for capturing a single cell, and at least one output channel in fluid connection with the at least one trapping structure, wherein the at least one trapping structure extends from one side of the feeding channel substantially perpendicular to longitudinal axis of the feeding channel, the at least one trapping structure possessing an aperture at its end opposite to the fluid channel and in fluid communication with an output channel, said aperture being configured to provide a narrow section such that the nucleus of a cell captured in the trapping structure cannot pass through said narrow section into the output channel.

First claim

1 . A microfluidic device comprising at least one microfluidic structure for differential extraction of nuclear and extra-nuclear constituents of a single cell, said microfluidic structure comprising:
a feeding channel for receiving a volume of a sample containing at least one cell, at least one trapping structure for capturing a single cell, and at least one outlet channel in fluid connection with the at least one trapping structure,
wherein the at least one trapping structure extends from one side of the feeding channel substantially perpendicular to longitudinal axis of the feeding channel,
the at least one trapping structure possessing an aperture at its end opposite to the fluid channel and in fluid communication with an outlet channel, said aperture being configured to provide a narrow section such that the nucleus of a cell captured in the trapping structure cannot pass through said narrow section into the outlet channel.

2 . The microfluidic device according to claim 1 , further comprising at least one buffer channel in fluid connection with the feeding channel, wherein the at least one buffer channel converges with the feeding channel at the side of the feeding channel opposite to the at least one trapping structure, and—with respect to the direction of flow within the feeding channel—at a position along the feeding channel preceding the position of the at least one trapping structure.

3 . The microfluidic device according to claim 1 , comprising two or more buffer channels.

4 . The microfluidic device according to claim 1 , wherein the at least one buffer channel or the two or more buffer channel converge(s) with the feeding channel in an angle of less than 90°, preferably in an angle in the range of about 30° to about 70°, more preferably in an angle in the range of about 40° to about 60°, and most preferably in an angle in the range of about 45° to about 55°.

5 . The microfluidic device according to claim 1 , wherein the narrow section has in inner diameter in the range of about 1 μm to about 4 μm.

6 . The microfluidic device according to claim 1 , wherein the outlet channel comprises two or more legs.

7 . The microfluidic device according to claim 1 , wherein the outlet channel or the legs of the outlet channel is/are is in fluid connection with at least one auxiliary chamber for detecting and/or analyzing at least one constituent of the cell.

8 . The microfluidic device according to claim 1 , wherein the microfluidic structure comprises at least one valve for directing the flow of fluid within the microfluidic structure.

9 . The microfluidic device according to claim 8 , wherein the inlet and/or the outlet of the feeding channel, the inlet and/or outlet of the at least one buffer channel, the inlet and/or outlet(s) of the outlet channel and/or the diversion within the outlet channel to the legs comprise the valve.

10 . A method of manufacturing a microfluidic device as defined in claim 9 , wherein the microfluidic structure is produced by injection molding a polymer, and subsequently sealing the channels by bonding a polymer film to the molded structure.

11 . Use of a microfluidic device according to claim 9 for differentially extracting nuclear and extra-nuclear constituents of a cell.

12 . The use according to claim 11 , wherein the nuclear and/or extra-nuclear constituents are nucleic acid molecules.

13 . A method for differentially extracting nuclear and extra-nuclear constituents of a single cell, the method comprising the steps of:
providing at least one cell to the feeding channel of a microfluidic device according to claim 9 ; capturing the at least one cell in the at least one trapping structure; lysing the cell captured in the at least one trapping structure without affecting integrity of the cell's nucleus by supplying a first lysis buffer to the cell; releasing the extra-nuclear constituents of the cell into the outlet channel; transferring the extra-nuclear constituents of the cell from the outlet channel into an auxiliary chamber for further processing; lysing the cell's nucleus by supplying a second lysis buffer to the nucleus; releasing the constituents of the cell's nucleus into the outlet channel; and transferring the constituents of the cell's nucleus from the outlet channel to an auxiliary chamber for further processing.

14 . The method according to claim 13 , further comprising:
amplification of at least one nucleic acid sequence of the cell's nuclear constituents; and amplification of at least one nucleic acid sequence of the cell's extra-nuclear constituents.

15 . The method according to claim 14 , further comprises analyzing the nucleotide sequence of the amplification product of the at least one nucleic acid sequence of the cell's nuclear constituents.

Assignees

• Koninklijke Philips Nv
• Univ Danmarks Tekniske

Inventors

• Van Der Zaag Pieter Jan
• Marie Rodolphe Charly Willy
• Van Strijp Dianne Arnoldina Margaretha Wilhelmina
• Olesen Tom
• Vulders Roland Cornelis Martinus
• Kristensen Anders

Classifications

• B01L2300/0864

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

• B01L3/502761 Primary

  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

• B01L2200/0668

  Trapping microscopic beads · CPC title

• C12M47/06

  Hydrolysis; Cell lysis; Extraction of intracellular or cell wall material (lysis of microorganisms C12N1/06; extracting or separating nucleic acids from biological samples C12N15/1003) · CPC title

• B01L2400/0622

  distribution valves, valves having multiple inlets and/or outlets, e.g. metering valves, multi-way valves · CPC title