IP Library Granted Patent US 9,663,821
Granted Patent B2
US 9,663,821 · App. 14/960,754 · Granted May 30, 2017

Optical lens system and method for microfluidic devices

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Quick Facts
Patent No.
US 9,663,821
App. No.
14/960,754
Granted
May 30, 2017
Kind
B2
Abstract

An apparatus for imaging one or more selected fluorescence indications from a microfluidic device. The apparatus includes an imaging path coupled to least one chamber in at least one microfluidic device. The imaging path provides for transmission of one or more fluorescent emission signals derived from one or more samples in the at least one chamber of the at least one microfluidic device. The chamber has a chamber size, the chamber size being characterized by an actual spatial dimension normal to the imaging path. The apparatus also includes an optical lens system coupled to the imaging path. The optical lens system is adapted to transmit the one or more fluorescent signals associated with the chamber.

Claims (33)

1. A method of monitoring nucleic acid sequencing, the method comprising:

providing a fluidic device comprising:

a high-density matrix of reaction sites having a reaction site density of greater than or equal to 1,000 reaction sites per square centimeter;

at least one sample introduced into the high-density matrix; and

at least one amplification reagent introduced into the high-density matrix;

maintaining the reaction sites of the fluidic device at a constant temperature;

amplifying the at least one sample within the high-density matrix at the constant temperature;

sequencing the at least one sample within the high-density matrix at the constant temperature;

illuminating the fluidic device with electromagnetic radiation with an illumination system;

reducing chromatic aberration of light along an optical path;

capturing an image of a determined number of reaction sites simultaneously; and

collecting multiple images of the fluidic device, wherein collecting multiple images comprises:

collecting at least a first image at a first wavelength; and

collecting at least a second image at a second wavelength different from the first wavelength.

2. The method of claim 1 , wherein the high-density matrix of reaction sites has a reaction site density of greater than or equal to 2,500 reaction sites per square centimeter.

3. The method of claim 1 , wherein the high-density matrix of reaction sites has a reaction site density of greater than or equal to 4,000 reaction sites per square centimeter.

4. The method of claim 1 , wherein each reaction site has a volume of less than 10 nanoliters.

5. The method of claim 1 , wherein the electromagnetic radiation emitted by the illumination system has a beam diameter of up to 76 millimeters.

6. The method of claim 1 , wherein reducing chromatic aberration is carried out by an optical lens system comprising at least one zero-power optical element coupled to the optical path.

7. The method of claim 1 , wherein collecting multiple images further comprises capturing the multiple images over a time frame from about 1 millisecond to about 1 minute.

8. The method of claim 1 , wherein collecting multiple images is conducted while maintaining the high-density matrix at a constant temperature.

9. A system for monitoring nucleic acid sequencing, the system comprising:

a fluidic device having a high-density matrix of reaction sites with a reaction site density of greater than or equal to 1,000 reaction sites per square centimeter and configured to receive at least one sample and at least one amplification reagent, wherein the reaction sites of the fluidic device are maintained at a constant temperature during amplification and sequencing of the at least one sample within the high-density matrix;

an illumination system coupled to the fluidic device and configured to illuminate the fluidic device with electromagnetic radiation;

an optical lens system coupled to an optical path and configured to transmit the electromagnetic radiation along the optical path, wherein the optical lens system is configured to reduce chromatic aberration of light along the optical path; and

a detector configured to capture multiple images of the fluidic device, wherein each image simultaneously encompasses a determined number of reaction sites, wherein at least a first image is captured at a first wavelength and at least a second image is captured at a second wavelength different from the first wavelength.

10. The system of claim 9 , wherein the high-density matrix of reaction sites has a reaction site density of greater than or equal to 2,500 reaction sites per square centimeter.

11. The system of claim 9 , wherein the high-density matrix of reaction sites has a reaction site density of greater than or equal to 4,000 reaction sites per square centimeter.

12. The system of claim 9 , wherein each reaction site has a volume of less than 10 nanoliters.

13. The system of claim 9 , wherein the illumination system is configured to emit electromagnetic radiation having a beam diameter of up to 76 millimeters.

14. The system of claim 9 , wherein the optical lens system comprises at least one zero-power optical element.

15. The system of claim 9 , wherein the detector is configured to capture multiple images over a time frame of 1 millisecond to 1 minute.

16. The system of claim 9 , wherein the detector is configured to capture multiple images while the high-density matrix is maintained at a constant temperature.

Assignments (2)
CHANGE OF NAME Recorded Sep 15, 2022
From: FLUIDIGM CORPORATION
To: STANDARD BIOTOOLS INC.
Reel/Frame 061448/0305 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2017
From: UNGER, MARC A.; FACER, GEOFFREY RICHARD; CLERKSON, BARRY; CESAR, CHRISTOPHER G.; SWITZ, NEIL
To: FLUIDIGM CORPORATION
Reel/Frame 042131/0447 →