Optical systems and methods for biological analysis

Patent metadata

Field	Value
Publication number	US-11815460-B2
Application number	US-202217825222-A
Country	US
Kind code	B2
Filing date	May 26, 2022
Priority date	Sep 30, 2011
Publication date	Nov 14, 2023
Grant date	Nov 14, 2023

Abstract

A method of analyzing a plurality of biological sample volumes comprises emitting, along an excitation optical path toward a sample holder holding the plurality of biological sample volumes, electromagnetic radiation from a broadband LED, wherein the broadband LED emits the electromagnetic radiation across a range of wavelengths at a total output power of at least 5 watts and at a maximum intensity at a wavelength less than 600 nanometers and at an intensity less than 30 percent of the maximum intensity at a wavelength of 650 or 670 nanometers, and receiving, by a sensor, an electromagnetic emission transmitted from the sample holder along an emission optical path.

First claim

What is claimed is:

1. A method of analyzing a plurality of biological sample volumes, the method comprising:
emitting, along an excitation optical path toward a sample holder holding the plurality of biological sample volumes, electromagnetic radiation from a broadband LED, wherein the broadband LED emits the electromagnetic radiation across a range of wavelengths at a total output power of at least 5 watts and at a maximum intensity at a wavelength less than 600 nanometers and at an intensity less than 30 percent of the maximum intensity at a wavelength of 650 or 670 nanometers,
passing the electromagnetic radiation emitted from the broadband LED through a first lens along the excitation optical path, the first lens directing the electromagnetic radiation from the broadband LED to the sample holder;
receiving, by a sensor, an electromagnetic emission transmitted from the sample holder along an emission optical path; and
passing the electromagnetic emission through a second lens disposed along the emission optical path between the sample holder and the sensor.

2. The method of claim 1 , wherein the electromagnetic emission comprises fluorescence.

3. The method of claim 1 , wherein the maximum intensity of the broadband LED is at a wavelength less than 550 nanometers and the intensity of the broadband LED that is less than 30 percent of the maximum intensity is at the wavelength of 650 nanometers.

4. The method of claim 1 , further comprising filtering the range of wavelengths such that the sample holder receives a subrange of the range of wavelengths of the electromagnetic radiation.

5. The method of claim 1 , further comprising selecting the sample holder from a plurality of formats of sample holders, the plurality of formats differing with respect to one or more of a number of reaction sites, a volumetric capacity of a reaction site, and a type of reaction site.

6. The method of claim 1 , wherein the plurality of biological sample volumes are held in the sample holder at a respective plurality of reaction sites, each reaction site configured to hold a biological sample volume of less than or equal to 5 nanoliters.

7. The method of claim 6 , wherein each reaction site is configured to hold a biological sample volume of less than or equal to 1 nanoliter.

8. The method of claim 1 , wherein each of the plurality of biological sample volumes is less than or equal to 5 nanoliters and the electromagnetic radiation directed to the sample holder is sufficient to excite one or more fluorescent dyes when contained in the plurality of biological sample volumes.

9. The method of claim 1 , wherein the plurality of biological sample volumes are held by a plurality of through holes of the sample holder.

10. The method of claim 1 , further comprising subjecting the sample holder to thermal cycling.

11. The method of claim 1 , further comprising subjecting the plurality of biological sample volumes to a polymerase chain reaction assay.

12. The method of claim 1 , further comprising determining the presence or absence of a target nucleic acid in each of the plurality of biological sample volumes based on the electromagnetic emission received by the sensor.

13. The method of claim 1 , wherein the sensor is chosen from a CMOS sensor array or a CCD sensor array.

14. The method of claim 1 , wherein the electromagnetic emission received by the sensor corresponds to data useful for a qPCR and/or dPCR biological sample analysis.

15. The method of claim 1 , wherein the electromagnetic emission received by the sensor results from a polymerase chain reaction assay to which the plurality of biological sample volumes are subjected.

16. The method of claim 1 , wherein the electromagnetic emission received by the sensor comprises fluorescence from one or more fluorescent dyes in one or more of the plurality of biological sample volumes.

17. The method of claim 16 , wherein the one or more fluorescent dyes are one or more of FAM, VIC, or ROX dyes.

Assignees

• Life Technologies Corp

Inventors

• Maher Kevin
• Chen Mingsong
• Freudenthal Jacob K
• Boo Kuan Moon
• Lau Soo Yong
• Fortescue David
• Shen Ming
• Soh Woon Liang Terence

Classifications

• G01N21/6486 Primary

  Measuring fluorescence of biological material, e.g. DNA, RNA, cells (G01N21/6428 takes precedence) · CPC title

• G01N21/6428

  Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" (in vivo A61B5/00; immunoassay G01N33/53) · CPC title

• G01N21/6452 Primary

  Individual samples arranged in a regular 2D-array, e.g. multiwell plates · CPC title

• G01N2021/6471

  Special filters, filter wheel · CPC title

• G01N2021/6478

  Special lenses · CPC title