Ultra-sensitive detection method using photoluminescent particles

Patent metadata

Field	Value
Publication number	US-12399124-B2
Application number	US-201816635515-A
Country	US
Kind code	B2
Filing date	Aug 3, 2018
Priority date	Aug 4, 2017
Publication date	Aug 26, 2025
Grant date	Aug 26, 2025

Abstract

A process for ultrasensitive in vitro detection and/or quantification of a substance of interest in a sample is performed by detecting the luminescence emission by photoluminescent inorganic nanoparticles. The process includes (i) use of photoluminescent particles comprising a photoluminescent inorganic nanoparticle consisting of a crystalline matrix having at least 10 3 rare-earth ions, and coupled to a targeting agent for the substance to be analyzed, under conditions conducive to their association with the sample substance to be analyzed; (ii) exciting the rare-earth ions of the particles by an illumination device having a power of at least 50 mW and an excitation intensity of at least 1 W/cm 2 ; (iii) detecting the luminescence emission by the particles after single-photon absorption; and (iv) determining the presence and/or concentration of the substance by interpreting said luminescence measurement. This process can be used for in vitro diagnostic purposes and as an in vitro diagnostic kit.

First claim

The invention claimed is:

1. A process for the ultrasensitive in vitro detection and/or quantification of a target substance of biological or chemical interest by detecting luminescence emission by photoluminescent inorganic nanoparticles, comprising at least the following steps:
providing a sample having the target substance in an amount below 10 pM;
immobilizing the target substance to a functionalized surface;
providing photoluminescent particles to the immobilized target substance on the functionalized support to associate with the target substance, the photoluminescent particles consisting, in whole or in part, of a photoluminescent inorganic nanoparticle consisting of a crystalline matrix having at least 10 3 rare-earth ions, and coupled to at least one targeting agent for the target substance to be analyzed, under conditions conducive to their association with the target substance to be analyzed of the sample, said nanoparticles having an average size greater than or equal to 20 nm and strictly less than 1 μm, and being capable of emitting luminescence after absorption of a photon;

wherein the nanoparticle is of the following formula (I):
(A 1-x Ln x ) a (M p O q )  (I)

wherein:
M represents one or more elements capable of associating with oxygen (O) to form a crystalline compound;
Ln corresponds to one or more luminescent lanthanide ion(s);
A corresponds to one or more constituent ion(s) of the crystalline matrix whose electronic levels are not involved in the luminescence process;
0<x<1; and
the values of p, q and a are such that the electroneutrality of (A 1-x Ln x ) a (M p O q ) is respected;
illuminating of the rare-earth ions of the photoluminescent particles associated with the target substance, by an illumination device, with a power of at least 50 mW, and an excitation intensity of at least 1 W/cm 2 ;
detecting luminescence emitted by the photoluminescent particles after single-photon absorption, and
determining of the presence and/or concentration of the substance by interpretation of said luminescence measurement, where appropriate by reference to a standard or calibration, wherein the target substance is determined to be present in the sample in an amount below 10 pM;

said process providing detection and/or quantification of a substance of interest present in a sample in a content strictly below 10 pM; and
the process using a light intensity 2D detection device comprising a single detector allowing simultaneous measurement of the emission signal of nanoparticles from different areas corresponding to different target substances to be analyzed on the surface of the functionalized support and does not require any movement of the support or the excitation beam.

2. The process as claimed in claim 1 , wherein the substance to be analyzed of said sample is previously immobilized on the surface of a support, said surface being passivated so that said luminescent particles do not attach thereto in the absence of the substance to be analyzed.

3. The process as claimed in claim 1 , wherein the sample is a biological sample.

4. The process as claimed in claim 1 , for the detection and/or quantification of biomarkers, antibodies, DNA and/or RNA in a biological sample.

5. The process as claimed in claim 1 , wherein said targeting agent is selected from a polyclonal or monoclonal antibody, an antibody fragment, a nanobody, an oligonucleide, a peptide, a hormone, a ligand, a cytokine, a peptidomimetic, a protein, a carbohydrate, a chemically modified protein, a chemically modified nucleic acid, a chemically modified carbohydrate which targets a known cell surface protein, an aptamer, a protein and DNA/RNA assembly or a chloroalkane.

6. The process as claimed in claim 1 , wherein the product between the doping rate of rare-earth ions and the quantum efficiency of the emission from the nanoparticle is maximized.

7. The process as claimed in claim 1 , wherein the nanoparticles have an emission lifetime greater than or equal to 5 μs.

8. The process as claimed in claim 1 , wherein the nanoparticles have an average size of between 20 nm and 500 nm.

9. The process as claimed in claim 1 , wherein the lanthanide ions are selected from europium (Eu), dysprosium (Dy), samarium (Sm), praseodymium (Pr), neodymium (Nd), erbium (Er), ytterbium (Yb), cerium (Ce), holmium (Ho), terbium (Tb), thulium (Tm) and mixtures thereof.

10. The process as claimed in claim 1 , the nanoparticles being of formula:
A 1-x Ln x VO 4(1-y) (PO 4 ) y   (II)

wherein:
A is selected from yttrium (Y), gadolinium (Gd), lanthanum (La), lutetium (Lu) and mixtures thereof;
Ln is selected from europium (Eu), dysprosium (Dy), samarium (Sm), neodymium (Nd), erbium (Er), ytterbium (Yb), thulium (Tm), terbium (Tb) and mixtures thereof;
0<x<1; and
0≤y<1.

11. The process as claimed in claim 10 , wherein said nanoparticles of formula (II) have on their surface tetraalkylammonium cations.

12. The process as claimed in claim 11 , said nanoparticles being of formula (II′)
A 1-x Ln x VO 4(1-y) (PO 4 ) y ·(NR 4 + ) z   (II′)

wherein:
A is selected from yttrium (Y), gadolinium (Gd), lanthanum (La), lutetium (Lu) and mixtures thereof;
Ln is selected from europium (Eu), dysprosium (Dy), samarium (Sm), neodymium (Nd), erbium (Er), ytterbium (Yb), thulium (Tm), terbium (Tb) and mixtures thereof;
0<x<1;
0≤y<10;
R, which may be identical or different, represent a C 1 -C 6 -alkyl; and
z represents the number of tetraalkylammonium cations NR 4 + located on the surface of said nanoparticle.

13. The process as claimed in claim 1 , wherein said nanoparticles are of formula Y 1-x Eu x VO 4 , wherein 0<x<1.

14. The process as claimed in claim 1 , wherein the nanoparticles have, at the end of their synthesis, a zeta potential, denoted ζ, less than or equal to −28 mV, in aqueous medium of pH≥5, and of ionic conductivity strictly less than 100 μS·cm −1 .

15. The process as claimed in claim 2 , further comprising at least the following steps:
(a) providing a support whose surface is previously passivated and functionalized with a targeting agent for the substance to be detected/quantified;
(b) contacting said sample to be analyzed with the support of step (a) under conditions conducive to the association of said substance with the targeting agent; and
(c) contacting the photoluminescent particles coupled with at least one targeting agent with said support from step (b) to associate the particles with said substance immobilized on the surface of the support.

16. The process as claimed in claim 2 , wherein said support is of the slide, multiwell plate, microplate, membrane gel, strip or microchannel type.

17. The process as claimed in claim 2 , wherein the excitation is carried out with a laser excitation beam oriented so as to form an angle of incidence greater than or equal to 55° with the vertical of the support having at the surface said particles associated with the substance to be analyzed.

18. The process as claimed in claim 2 , comprising the excitation of the particles by evanescent wave.

19. The process as claimed in claim 1 , wherein the lifetime of emission by the nanoparticles is greater than or equal to 1 μs, the detection of the light intensity comprising a time-resolved detection of the emission.

20. The process as claimed in claim 1 , for the simultaneous detection and/or quantification of at least two different substances in a sample.

21. The process as claime

Assignees

• Ecole Polytech
• Centre Nat Rech Scient

Inventors

• Preira Pascal
• Richly Maximilian
• Bouzigues Cédric
• Alexandrou Antigoni
• Gacoin Thierry

Classifications

• Y10S977/958

  Of biomolecule property · CPC title

• Y10S977/957

  Of chemical property or presence · CPC title

• Y10S977/92

  Detection of biochemical · CPC title

• A61K49/105

  the metal complex being Gd-DTPA · CPC title

• G01N2458/40

  Rare earth chelates · CPC title