Microfluidic devices with integrated resistive heater electrodes including systems and methods for controlling and measuring the temperatures of such heater electrodes

Patent metadata

Field	Value
Publication number	US-9492826-B2
Application number	US-16501308-A
Country	US
Kind code	B2
Filing date	Jun 30, 2008
Priority date	Aug 29, 2007
Publication date	Nov 15, 2016
Grant date	Nov 15, 2016

Abstract

The invention relates to methods and devices for control of an integrated thin-film device with a plurality of microfluidic channels. In one embodiment, the microfluidic device includes a microfluidic chip comprising a first zone having a plurality of microfluidic channels and a second zone having a plurality of microfluidic channels, wherein the microfluidic channels in the first and second zones are in fluid communication. The microfluidic device further comprising a thin-film heater in thermal communication with each of the microfluidic channels in the first and second zones. The microfluidic device also includes a control system configured to independently control the temperature of each of the thin-film heaters using pulse width modulation (PWM) control signals that are optimized for each of the thin-film heaters.

First claim

What is claimed is:

1. In a microfluidic device incorporating thin-film heaters within a plurality of microfluidic channels to effect a biological reaction with multiple steps each requiring a different temperature, a method of controlling the microfluidic with pulse width modulation (PWM) comprising:
generating a set of calibration data while calibrating a modulation frequency with a temperature by measuring a cooling rate of the thin-film heaters between pulses and adjusting the modulation frequency based upon the measured rate;
using the calibration data to generate a PWM control signal for the thin-film heaters designed to bring the heaters to a desired temperature for a first step in the biological process;
adjusting the PWM signal to achieve a temperature for an appropriate time required by said first step; and
adjusting the PWM signal to achieve a desired temperature for a second step in the biological process.

2. The method of claim 1 , wherein the PWM signals are differentially sequenced to minimize current draw and power spiking on the system power supply.

3. The method of claim 2 , wherein differentially sequencing the PWM signals comprises a multiplexed sequence among 3 or more microfluidic channels.

4. The method of claim 1 , wherein the biological reaction is a polymerase chain reaction.

5. The method of claim 4 , wherein the polymerase chain reaction occurs within a first temperature zone.

6. The method of claim 1 , wherein the biological reaction is a high resolution thermal melt.

7. The method of claim 6 , wherein the high resolution thermal melt occurs within a second temperature zone.

8. The method of claim 1 , wherein a thin-film heater is associated with each microfluidic channel.

9. The method of claim 1 , wherein a common electrical contact is associated with all of the microfluidic channels.

10. The method of claim 1 , wherein the step of generating calibration data comprises:
(a) applying electrical power to all heater electrodes;
(b) measuring a voltage drop across each of the heater electrodes to determine individual electrode resistance values;
(c) computing a nominal heater power based on the individual heater electrode resistance values;
(d) applying the nominal heater power to the heater electrodes for a pre-determined calibration pulse time;
(e) collecting heater electrode resistance measurements for a predetermined collection time at a predetermined sampling rate;
(f) using the measurements to compute a thermal decay time constant reflecting the rate at which the heater electrode cools when the power is off; and
(g) computing an optimal pulse width modulation frequency based on the decay time information.

11. The method of claim 1 , wherein the biological reaction is a polymerase chain reaction in a first temperature zone and a high resolution thermal melt in a second temperature zone.

12. A method of controlling a microfluidic device comprising a plurality of thin-film heaters that heat a plurality of parallel microfluidic channels to effect a biological reaction, said method comprising:
providing control circuitry configured to generate PWM control signals to drive the thin-film heaters, wherein each channel is in thermal communication with at least one of the plurality of thin-film heaters;
differentially sequencing the pulse width modulation control signals to said thin-film heaters, wherein the PWM control signals associated with different channels are phase shifted relative to each other so as to minimize current draw and power spiking on a system supplying power to said microfluidic device.

13. The method of claim 12 , wherein the pulse with modulation control signals are differentially sequenced among 3 or more microfluidic channels.

14. The method of claim 12 , wherein the pulse with modulation control signals are differentially sequenced among two banks of parallel microfluidic channels.

15. The method of claim 12 , wherein the biological reaction is a polymerase chain reaction.

16. The method of claim 12 , wherein the biological reaction is a thermal melt.

17. The method of claim 12 , wherein a thin-film heater is associated with each microfluidic channel.

18. The method of claim 12 , wherein a common electrical contact is associated with all of the microfluidic channels.

Assignees

• Hanagata Takayoshi
• Inoue Hiroshi
• Dale Gregory A
• Hasson Kenton C
• Canon Us Life Sciences Inc

Inventors

• Hanagata Takayoshi
• Inoue Hiroshi
• Dale Gregory A
• Hasson Kenton C

Classifications

• B01L7/525 Primary

  with physical movement of samples between temperature zones · CPC title

• G01K7/16

  using resistive elements · CPC title

• B01L2300/1805

  Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks · CPC title

• B01L7/52 Primary

  with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples · CPC title

• C12Q1/686

  Polymerase chain reaction [PCR] · CPC title