Granted Patent B2

US 12,551,897 · App. 17/722,243 · Granted Feb 17, 2026

Inventors: Justin Buckland (Royston, GB); Tom Jellicoe (Royston, GB); Alex Stokoe (Royston, GB); Amaru Araya-Williams (Royston, GB)

Assignee: Lex Diagnostics Ltd.

B01L7/52B01L3/5027C12Q1/6806C12Q1/686B01L2300/0883B01L2300/1827B01L2300/1883

Abstract

Claims (47)

1 . A method of performing nucleic acid amplification with rapid polymerase chain reaction (PCR) thermocycling, the method comprising

obtaining a liquid sample comprising nucleic acid;

introducing the sample and a polymerase enzyme into a reaction cell enclosing a flat reaction volume, wherein the sample is heated within the flat reaction volume with a heater element and cooled within the flat reaction volume with a heat sink,

wherein one side of the heater element contacts the reaction cell, and an opposite side of the heater element contacts a heater support arranged between the heater element and the heat sink,

wherein the heater support provides a thermal resistance R T , and

wherein the thermal resistance of the heater support between the heater element and the heat sink is between about 20 Kelvin/watt and about 5 Kelvin/watt;

conducting an initial hot-start of the sample in the flat reaction volume to activate the polymerase enzyme;

performing PCR thermocycling with a cycle time of about 5 seconds or less, wherein a cycle includes at least raising a temperature of the sample in the flat reaction volume from a low temperature to a high temperature and back down to the low temperature; and

detecting the amplified DNA,

wherein the sample is heated and cooled as one continuous body of liquid within the flat reaction volume, and

wherein all thermocycling of the sample occurs in the flat reaction volume within the reaction cell without moving the sample between two different temperature zones that are spatially separated.

2 . The method of claim 1 , wherein the nucleic acid is DNA or RNA.

3 . The method of claim 1 , wherein the sample is not partitioned into disconnected sub-samples and is heated and cooled as one continuous body of liquid without solid, immiscible fluid, or gaseous barriers between subsamples.

4 . The method of claim 1 , wherein the flat reaction volume comprises two or more fluidically connected regions that are all heated by a single heater element.

5 . The method of claim 1 , wherein motion of the liquid sample is stopped during thermocycling.

6 . The method of claim 1 , wherein between 30 and 50 cycles of PCR amplification are completed in less than about 200 seconds.

7 . The method of claim 1 , wherein the cycle time is about 0.4 seconds to about 5.0 seconds.

8 . The method of claim 1 , wherein the cycle time is about 0.8 seconds to about 1.6 seconds.

9 . The method of claim 1 , wherein the cycle time is about 1.0 second to about 2.0 seconds.

10 . The method of claim 1 , wherein one cycle includes at least raising a temperature of the sample from a low temperature of about 55-60° C. to a high temperature of about 90-95° C. and back down to the low temperature.

11 . The method of claim 1 , wherein the PCR is multiplexed PCR.

12 . The method of claim 1 , wherein the PCR is quantitative PCR, wherein a concentration of amplified DNA is monitored over time.

13 . The method of claim 1 , wherein the PCR is droplet-free digital PCR.

14 . The method of claim 1 , wherein the initial hot-start is run for less than about 20 seconds.

15 . The method of claim 1 , wherein the heater element used to heat the flat reaction volume is driven at a power of at least about 5 watts to about 20 watts.

16 . The method of claim 4 , wherein the two or more fluidically connected regions are all heated by a single heater element driven at a power of at least about 5 watts per region.

17 . The method of claim 1 , wherein the flat reaction cell has an internal height of less than about 250 microns.

18 . The method of claim 1 , wherein the temperature of the sample in the flat reaction volume is raised and lowered at a temperature ramp rate of at least 70° C./s.

19 . The method of claim 1 , further comprising driving the heater element by a sinusoidal electrical drive controlled at a frequency f DRIVE that is applied to the heater element to generate an oscillating heat output at a frequency of 2×f DRIVE , where f DRIVE satisfies the condition:

f

DRIVE

≤

1

2

⁢

π

⁢

D

W

H

W

2

wherein D W is a thermal diffusion coefficient of a thin outer wall of the reaction cell that contacts the heater element, and H W is a thickness of the thin outer wall.

20 . The method of claim 19 , wherein f DRIVE is about 23 Hz to about 2.3 Hz, and the thin outer wall has a thickness of about 24 microns to about 76 microns.

21 . The method of claim 19 , wherein the thin outer wall has a thickness H W of about 24 microns to about 76 microns.

22 . The method of claim 19 , wherein the thin outer wall has a thermal diffusion time of less than 0.07 seconds.

23 . The method of claim 19 , wherein the thin outer wall has a thermal diffusion time of less than 0.007 seconds.

Assignments (1)

Priority Claims (1)

Continuity (4)

References Cited (221)