Granted Patent B2

US 12,351,866 · App. 17/438,012 · Granted Jul 8, 2025

Inventors: Hidenori Nagai (Ikeda, JP); Satoru Iwanami (Tokyo, JP)

Assignees: NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY; KYORIN PHARMACEUTICAL CO., LTD.

C12Q1/686B01L7/525

Abstract

Claims (15)

1. A reciprocal-flow-type nucleic acid amplification method performing thermal cycling, the method comprising

moving a sample liquid in a microchannel by a liquid delivery mechanism that is open to atmospheric pressure when liquid delivery is stopped, wherein the microchannel includes at least a curved channel corresponding to a denaturation temperature zone, a curved channel corresponding to an elongation-annealing temperature zone, a linear or curved intermediate channel that connects the curved channel corresponding to the denaturation temperature zone and the curved channel corresponding to the elongation-annealing temperature zone, and a connector connectable to the liquid delivery mechanism for enabling movement of the sample liquid, and

measuring fluorescence intensities for each thermal cycle at a predetermined point on the curved channel corresponding to the denaturation temperature zone and at a predetermined point on the curved channel corresponding to the elongation-annealing temperature zone to perform real-time PCR, wherein the predetermined point on the curved channel corresponding to the denaturation temperature zone is the position after one to four turns or curved portions from the intermediate channel, and the predetermined point on the curved channel corresponding to the elongation-annealing temperature zone is the position after one to four turns or curved portions from the intermediate channel.

2. A nucleic acid amplification method comprising the following steps:

step 1 of mounting a chip for nucleic acid amplification on a substrate of a reciprocal-flow-type nucleic acid amplification device being capable of performing real-time PCR by measuring fluorescence intensity for each thermal cycle, the reciprocal-flow-type nucleic acid amplification device including a heater to form a denaturation temperature zone and an elongation-annealing temperature zone, a fluorescence detector to measure a fluorescence intensity of a sample liquid present in the denaturation temperature zone, a fluorescence detector to measure a fluorescence intensity of the sample liquid present in the elongation-annealing temperature zone, a liquid delivery mechanism to allow the sample liquid to move between the denaturation temperature zone and the elongation-annealing temperature zone, and to become open to atmospheric pressure when liquid delivery is stopped, the substrate on which the chip for nucleic acid amplification is mounted, and a control mechanism to receive an electric signal related to the movement of the sample liquid from the fluorescence detector and control the drive of the liquid delivery mechanism,

the chip for nucleic acid amplification including at least one microchannel, the at least one microchannel including a curved channel corresponding to the denaturation temperature zone, a curved channel corresponding to the elongation-annealing temperature zone, a linear or curved intermediate channel that connects the curved channel corresponding to the denaturation temperature zone and the curved channel corresponding to the elongation-annealing temperature zone, and a connector to connect the liquid delivery mechanism of the nucleic acid amplification device to one or both ends of the microchannel;

step 2 of connecting the connector for the liquid delivery mechanism in the microchannel to the liquid delivery mechanism;

step 3 of reciprocating the sample liquid between the two curved channels in the microchannel by the liquid delivery mechanism to perform thermal cycling; and

step 4 of measuring fluorescence intensities of the sample liquid for each thermal cycle at a predetermined point on the curved channel corresponding to the denaturation temperature zone and at a predetermined point on the curved channel corresponding to the elongation-annealing temperature zone by the fluorescence detectors.

3. The nucleic acid amplification method according to claim 1 , wherein the liquid delivery mechanism is a microblower or fan.

4. The nucleic acid amplification method according to claim 1 , wherein the intermediate channel that connects the curved channels is a linear channel.

5. The nucleic acid amplification method according to claim 4 , the method comprising a step of measuring a fluorescence intensity of the sample liquid for each thermal cycle at a predetermined point on the intermediate channel.

6. A reciprocal-flow-type nucleic acid amplification method performing thermal cycling, the method comprising

moving a sample liquid in a microchannel by a liquid delivery mechanism that is open to atmospheric pressure when liquid delivery is stopped wherein the microchannel includes at least a curved channel corresponding to a denaturation temperature zone, a curved channel corresponding to an elongation-annealing temperature zone, a linear intermediate channel that connects the curved channel corresponding to the denaturation temperature zone and the curved channel corresponding to the elongation-annealing temperature zone, and a connector connectable to the liquid delivery mechanism for enabling movement of the sample liquid, and

measuring fluorescence intensities for each thermal cycle at a predetermined point on the curved channel corresponding to the denaturation temperature zone and at a predetermined point on the curved channel corresponding to the elongation-annealing temperature zone to perform real-time PCR, wherein a distance between a fluorescence measurement point on the intermediate channel and a fluorescence measurement point on the denaturation temperature zone is 8 mm or more.

Assignments (4)

Priority Claims (1)

Continuity (1)

References Cited (30)