Method for conducting reactions involving biological molecules in plugs in a microfluidic system

Patent metadata

Field	Value
Publication number	US-11478799-B2
Application number	US-201815926985-A
Country	US
Kind code	B2
Filing date	Mar 20, 2018
Priority date	May 9, 2002
Publication date	Oct 25, 2022
Grant date	Oct 25, 2022

Abstract

The present invention provides microfabricated substrates and methods of conducting reactions within these substrates. The reactions occur in plugs transported in the flow of a carrier-fluid.

First claim

We claim:

1. A method of forming a plurality of plugs and conducting a reaction in at least one thereof, the method comprising the steps of:
providing a microfluidic device comprising a substrate having at least a first channel and a second channel intersecting each other at a plug-forming junction;
introducing to the first channel of the microfluidic device a stream of a first plug fluid containing at least one biological molecule and introducing to the first channel a stream of a second plug fluid containing one or more reagents for conducting the reaction with the at least one biological molecule of the first plug fluid;
continuously coflowing the stream of the first plug fluid and the stream of the second plug fluid with one another and through the first channel of the microfluidic device towards the plug-forming junction such that at least one biological molecule of the first plug fluid and the one or more reagents, of the second plug fluid, for conducting a reaction with the at least one biological molecule coflow with one another prior to contact with a carrier fluid and prior to plug formation;
continuously flowing a stream of a carrier fluid comprising an oil immiscible with the streams of first and second plug fluids through the second channel of the microfluidic device towards the plug-forming junction, wherein the carrier fluid comprises a fluorosurfactant that comprises an oligoethylene glycol (OEG) terminal end to which an OEG is linked;
forming a plurality of plugs comprising a portion of the coflowing and streaming first and second plug fluids containing the at least one biological molecule and the one or more reagents, respectively, by partitioning the continuously coflowing streams of first and second plug fluids with the continuously flowing stream of carrier fluid at the plug-forming junction of the first and second channels, each of the plurality of plugs being substantially surrounded by the carrier fluid, wherein at least one of the plurality of plugs comprises the at least one biological molecule and the one or more reagents for conducting the reaction with the at least one biological molecule; and
providing conditions suitable for a polymerase chain reaction (PCR) to occur in the at least one plug involving the at least one biological molecule and the one or more reagents to form a PCR product.

2. The method of claim 1 , wherein the at least one biological molecule is DNA or RNA.

3. The method of claim 1 , further comprising detecting the reaction product.

4. The method of claim 3 , wherein detecting is optically detecting.

5. The method of claim 1 , wherein the oil is a fluorinated oil.

6. The method of claim 1 , wherein the step of forming the plurality of plugs comprises a plurality of plugs some of which contain at least one biological molecule and others are free of biological molecules.

7. The method of claim 1 , wherein the providing conditions suitable for the reaction step comprises heating.

8. The method of claim 1 , wherein each of the plurality of plugs is substantially surrounded on all sides by the immiscible carrier fluid.

9. The method of claim 1 , further comprising the step of collecting the plurality of plugs in a segment of tubing or the sample tube through an outlet of the microfluidic device positioned downstream of the plug-forming junction, wherein the plugs remain separated by the immiscible carrier fluid.

10. The method of claim 1 , further comprising the step of dispensing the plurality of plugs into a segment of tubing or a sample tube from an outlet of the microfluidic device positioned downstream of the plug-forming junction using a driving force, wherein the plugs in the segment of tubing or the sample tube remain separated by the immiscible carrier fluid.

11. The method of claim 1 , further comprising the step of flowing the plurality of plugs and immiscible carrier fluid into a non-fluorinated channel of the microfluidic device positioned downstream of the plug-forming junction.

12. The method of claim 11 , wherein the immiscible carrier fluid comprises a fluorinated oil and a fluorinated surfactant comprising a hydrophilic head group, wherein the fluorinated surfactant is present at a concentration such that surface tension at the plug fluid/channel wall interface is higher than surface tension at the plug fluid/carrier fluid interface.

13. The method of claim 1 , wherein the fluorosurfactant is of the formula:

wherein m is 0, 3, 4, 5, or 6; and n is an integer of no less than 16.

Assignees

• Univ Chicago

Inventors

• Ismagilov Rustem F
• Tice Joshua David
• Gerdts Cory John
• Zheng Bo

Classifications

• B01J2219/00722

  Nucleotides · CPC title

• G01N1/28

  Preparing specimens for investigation {including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q}(mounting specimens on microscopic slides G02B21/34; means for supporting the objects or the materials to be analysed in electron microscopes H01J37/20 {; laboratory gas handling apparatus B01L5/00}) · CPC title

• B01L2200/12

  Specific details about manufacturing devices · CPC title

• B01J2219/00783

  Laminate assemblies, i.e. the reactor comprising a stack of plates · CPC title

• B01F25/4331

  Mixers with bended, curved, coiled, wounded mixing tubes or comprising elements for bending the flow · CPC title