Method for detecting a reversibly photoswitchable chemical species in a sample

Patent metadata

Field	Value
Publication number	US-12504374-B2
Application number	US-202017784639-A
Country	US
Kind code	B2
Filing date	Nov 27, 2020
Priority date	Dec 17, 2019
Publication date	Dec 23, 2025
Grant date	Dec 23, 2025

Abstract

A method for detecting a reversibly photoswitchable chemical species in a sample, includes the steps of: a) illuminating the sample with light suitable to be absorbed by the chemical species triggering a reaction affecting an optical property of the chemical species, the first light being periodically-modulated at a fundamental modulation frequency; b) measuring the evolution of the optical property; c) extracting at least one of an in-phase component at a frequency which is an even multiple of the fundamental modulation frequency; and a quadrature component at a frequency which is an odd multiple of the fundamental modulation frequency of a signal representing the evolution; and d) using the extracted component or components for detecting the chemical species. An apparatus for carrying out the method is also provided.

First claim

The invention claimed is:

1 . A method for detecting a reversibly photoswitchable chemical species in a sample, comprising the steps of:
a) illuminating the sample(S) with a first light at a first wavelength suitable to be absorbed by the chemical species triggering a reaction affecting at least one optical property of the chemical species, said first light being periodically-modulated at a fundamental modulation frequency; and b) measuring the evolution of the optical property of the chemical species; further comprises further comprising the steps of: c) extracting at least one of:
an in-phase component at a frequency which is an even multiple, different from zero, of the fundamental modulation frequency; and
a quadrature component at a frequency which is an odd multiple of the fundamental modulation frequency, greater than the fundamental modulation frequency itself,
of a signal representing said evolution; and d) using the extracted component or components for detecting the chemical species.

2 . The method of claim 1 , wherein the average intensity of the light and the fundamental modulation frequency are chosen so as:
either to maximize the amplitude of said or at least one said extracted component; or to minimize an interfering signal, at the frequency of said or at least one said extracted component, from a different chemical species in the sample.

3 . The method of claim 1 , wherein step a) further comprises illuminating the sample with a second light at a second wavelength, different from the first wavelength and suitable to be absorbed by the chemical species triggering said or another reaction affecting said optical property of the chemical species, said second light having a constant intensity.

4 . The method of claim 1 , wherein step a) further comprises illuminating the sample with a second light at a second wavelength, different from the first wavelength and suitable to be absorbed by the chemical species triggering said or a different reaction affecting said optical property of the chemical species, said second light being periodically modulated at the fundamental modulation frequency, in phase opposition with the first light.

5 . The method of claim 3 , wherein the ratio of the average intensities of the first and second light and the fundamental modulation frequency are chosen so as:
either to maximize the amplitude of said or at least one said extracted component; or to minimize an interfering signal, at the frequency of said or at least one said extracted component, from a different chemical species in the sample.

6 . The method of claim 1 , wherein steps a), b) and c) are repeated a plurality of times for different illumination conditions, corresponding to different values of the light intensity or intensities and of the fundamental modulation frequency and wherein step d) comprises using a plurality of signal components corresponding to said different illumination conditions for discriminating between a plurality of chemical species.

7 . The method of claim 6 , wherein step d) comprises applying a machine learning or unmixing method to said plurality of signal components for estimating absolute or relative concentration of said chemical species.

8 . The method of claim 1 , wherein light is modulated sinusoidally at the fundamental modulation frequency.

9 . The method of claim 1 , wherein light is modulated by a sinusoid at the fundamental modulation frequency multiplied by a pulse train at a repetition frequency which is a multiple of, and at least ten times larger than, the fundamental modulation frequency.

10 . The method of claim 9 , wherein steps a) and b) are carried out by light scanning microscopy.

11 . The method of claim 1 , wherein said chemical species is fluorescent and said optical property whose evolution is measured is the intensity of fluorescence emission.

12 . An apparatus for carrying out a method according to claim 1 , comprising:
at least a first controlled light source (LS1) configured for illuminating a sample with a first light at a first wavelength, said first light being periodically-modulated at a fundamental modulation frequency; a light detector (CAM) configured for measuring the evolution of an optical property of the sample; and a data processing device (DPD);
wherein the data processing device is configured for extracting at least one of an in-phase component at a frequency which is an even multiple, different from zero, of the fundamental modulation frequency and a quadrature component at a frequency which is an odd multiple, greater than the fundamental modulation frequency itself, of the fundamental modulation frequency of a signal representing said evolution; and for using the extracted component or components for detecting a chemical species in the sample.

13 . The apparatus of claim 12 , further comprising a second controlled light source (LS2) configured for illuminating the sample with a second light at a second wavelength, different from the first wavelength, said second light having a constant intensity.

14 . The apparatus of claim 12 , further comprising a second controlled light source (LS2) configured for illuminating the sample with a second light at a second wavelength, different from the first wavelength, said second light being periodically modulated at the fundamental modulation frequency, in phase opposition with the first light.

15 . The apparatus of claim 12 , further comprising a scanning device for illuminating the sample.

Assignees

• Centre Nat Rech Scient
• Ecole Normale Superieure De Paris
• Univ Sorbonne

Inventors

• Chouket Raja
• Croquette Vincent
• Espagne Agathe
• Jullien Ludovic
• Lemarchand Annie
• Le Saux Thomas
• Pellissier-Tanon Agnès
• Zhang Ruikang

Classifications

• G01N2021/6441

  with two or more labels · CPC title

• G01N2021/6419

  Excitation at two or more wavelengths · CPC title

• G01N21/6458

  Fluorescence microscopy (fluorescence microscopes per se G02B21/0076 and G02B21/16) · CPC title

• G01N21/6408 Primary

  with measurement of decay time, time resolved fluorescence · CPC title

• G01N21/6428 Primary

  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