Compositions, methods and systems for polymerase chain reaction assays

Patent metadata

Field	Value
Publication number	US-10676778-B2
Application number	US-201715818601-A
Country	US
Kind code	B2
Filing date	Nov 20, 2017
Priority date	Mar 8, 2013
Publication date	Jun 9, 2020
Grant date	Jun 9, 2020

Abstract

Methods, devices, systems and compositions for detecting nucleic acids in polymerase chain reaction assays, such as droplet digital polymerase chain reaction (ddPCR) assays, using intercalating dyes. A dual surfactant system with at least one fluorosurfactant and at least one non-ionic non-fluorosurfactant may be employed for droplet generation and nucleic acid detection.

First claim

We claim:

1. A composition, comprising:
a continuous phase including an oil and a fluorosurfactant mixture, wherein said fluorosurfactant mixture includes
a triblock copolymer comprising a first polyethylene glycol (PEG) block covalently linked to a respective polyhexafluoropropylene oxide (PFPE) block at each end of the first PEG block,
a diblock copolymer comprising a second PEG block covalently linked to a PFPE block at only one end of the second PEG block, and
a PFPE carboxylic acid; and

aqueous droplets suspended in the continuous phase and comprising nucleic acid, a non-ionic non-fluorosurfactant, and an intercalating dye;
wherein the first PEG block and each respective PFPE block of the triblock copolymer are linked to one another by an ester bond, and wherein the second PEG block and the PFPE block of the diblock copolymer are linked to one another by an ester bond.

2. The composition of claim 1 , wherein the triblock copolymer has the formula

wherein each of m 1 and m 2 is a number from about 10 to 100, and wherein n is a number from about 15 to 30.

3. The composition of claim 2 , wherein each of m 1 and m 2 is a number from about 20 to 40, and wherein n is a number from about 10 to 60.

4. The composition of claim 2 , wherein the diblock copolymer has the formula

wherein m 3 is a number from about 20 to 50, wherein n 2 is a number from about 8 to 30, and wherein R is H or an alkyl group.

5. The composition of claim 4 , wherein the PFPE carboxylic acid has the formula

wherein n is about 15 to 50.

6. The composition of claim 2 , wherein the PFPE carboxylic acid has the formula

wherein n is about 15 to 50.

7. The composition of claim 1 , wherein the diblock copolymer has the formula

wherein m 3 is a number from about 20 to 50, wherein n 2 is a number from about 8 to 30, and wherein R is H or an alkyl group.

8. The composition of claim 7 , wherein the PFPE carboxylic acid has the formula

wherein n is about 15 to 50.

9. The composition of claim 1 , wherein the PFPE carboxylic acid has the formula

wherein n is about 15 to 50.

10. The composition of claim 1 , wherein the non-ionic non-fluorosurfactant is a copolymer of ethylene oxide and propylene oxide.

11. The composition of claim 10 , wherein the non-ionic non-fluorosurfactant is a triblock copolymer of polyethylene oxide-polypropylene oxide-polyethylene oxide.

12. The composition of claim 11 , wherein the non-ionic non-fluorosurfactant is Pluronic®.

13. The composition of claim 12 , wherein the concentration of the Pluronic® is in a range from about 0.1%-3.0% (weight percent).

14. The composition of claim 1 , wherein the oil comprises a fluorous oil.

15. The composition of claim 14 , wherein the fluorous oil is 2-trifluoromethyl-3-ethoxydodeca-fluorohexane (HFE-7500) or 1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-(trifluoromethyl)pentane (HFE-7300).

16. The composition of claim 1 , wherein the intercalating dye includes EvaGreen® dye.

17. The composition of claim 1 , wherein the nucleic acid includes a target nucleic acid, and wherein only a subset of the droplets include a copy of the target nucleic acid.

18. The composition of claim 17 , wherein the aqueous droplets further comprise primers for amplification of the target nucleic acid.

19. The composition of claim 17 , wherein the aqueous droplets further comprise a thermostable polymerase.

20. The composition of claim 19 , wherein the aqueous droplets are configured to amplify the target nucleic acid when thermally cycled.

Assignees

• Bio Rad Laboratories

Inventors

• Lowe Adam
• Mcdermott Geoff
• Hindson Christopher M
• Chia Erin R
• Hiddessen Amy L
• Hindson Benjamin J
• Han Chunxiao
• Wang Yaqi

Classifications

• C12Q1/6804 Primary

  Nucleic acid analysis using immunogens (immunoassay G01N33/53) · CPC title

• C12Q1/6844

  Nucleic acid amplification reactions · CPC title

• C12Q2527/125

  Specific component of sample, medium or buffer · CPC title

• C12Q1/6851 Primary

  Quantitative amplification · CPC title

• C12Q2537/143

  Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis · CPC title