IP Library › Granted Patent US 12,618,834
Granted Patent B2
US 12,618,834 · App. 17/686,784 · Granted May 5, 2026

Measurement sample preparation method, analysis method, reagent, and reagent kit

Inventors: Yuki Shimaoka (Kobe, JP); Masaya Okada (Kobe, JP); Shigeki Iwanaga (Kobe, JP); Kazuki Bando (Suita, JP); Katsumasa Fujita (Suita, JP); Yasunori Nawa (Ikeda, JP); Satoshi Fujita (Ikeda, JP)
Assignees: SYSMEX CORPORATION; OSAKA UNIVERSITY; NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY
G01N33/54353G01N21/255G01N21/314G01N21/658G01N33/54346G01N33/588G01N33/6812G06N3/08G16C20/20G01N2201/121G01N2201/1296G16C20/70
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Quick Facts
Patent No.
US 12,618,834
App. No.
17/686,784
Granted
May 5, 2026
Kind
B2
Abstract

Disclosed is a preparation method for preparing a measurement sample comprising an aggregate of metal nanoparticles having an analyte bound thereto, the preparation method comprising: contacting the analyte with a linker to bind the analyte to the linker; and contacting the linker that has been bound to the analyte with the metal nanoparticles to bind the linker to the metal nanoparticles.

Claims (16)

1 . An analysis method for analyzing analytes in a sample using a spectroscopic analysis, the method comprising:

preparing a measurement sample comprising, wherein the preparing comprises:

contacting the analytes with linkers to bind the analytes to the linkers, whereby a plurality of complexes are formed, each complex having the analyte and the linker bound to the analyte;

contacting the complexes with metal nanoparticles to bind the complexes to the metal nanoparticles, whereby a plurality of first aggregates are formed in a solution, each first aggregate having the metal nanoparticle and the complex bound to the metal nanoparticle; and

adding an inorganic salt or an acid to the solution containing the plurality of the first aggregates, whereby a second aggregate is formed, the second aggregate consists of a plurality of the analytes, a plurality of the linkers and a plurality of the metal nanoparticles;

obtaining an optical spectrum from the second aggregates as a measurement sample; and

outputting information about a type of the analyte in the second aggregate on the basis of the obtained optical spectrum,

wherein the analyte is at least one substance selected from the group consisting of a single amino acid, a nucleic acid, a catecholamine, a polyamine, an organic acid, an extracellular vesicle and a virus.

2 . The analysis method according to claim 1 , wherein the analyte has a functional group, and the linker has a reactive group capable of reacting with the functional group.

3 . The analysis method according to claim 2 , wherein the functional group is at least one selected from the group consisting of an amino group, a carboxyl group and a hydroxyl group.

4 . The analysis method according to claim 3 , wherein the functional group is an amino group and the reactive group is at least one selected from the group consisting of an N-hydroxysuccinimide ester group, an isothiocyanate group, an isocyanate group, an acyl azide group, a sulfonyl chloride group, an aldehyde group, an imide ester group, a fluorobenzene group, an epoxide group, a carbodiimide group, a carbonate group, and a fluorophenyl ester group.

5 . The analysis method according to claim 4 , wherein the reactive group is an N-hydroxysuccinimide ester group, and the linker is at least one component selected from the group consisting of dithiobis(succinimidyl propionate), dithiobis(succinimidyl undecanoate), dithiobis(succinimidyl octanoate) and dithiobis(succinimidyl hexanoate).

6 . The analysis method according to claim 1 , wherein the metal nanoparticle is a nanoparticle, the nanoparticle being at least one metal selected from the group consisting of gold, silver, platinum, copper and palladium.

7 . The analysis method according to claim 1 , wherein a particle diameter of the metal nanoparticle is equal or greater than 10 nm and equal or smaller than 150 nm.

8 . The analysis method according to claim 1 , wherein the sample is blood, serum, plasma, saliva or a body fluid, or is a solution of the analytes in which water or a buffer solution is used as a solvent.

9 . The analysis method according to claim 1 , wherein the spectroscopic analysis is a surface enhanced Raman scattering analysis.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2022
From: SHIMAOKA, YUKI; OKADA, MASAYA; IWANAGA, SHIGEKI; BANDO, KAZUKI; FUJITA, KATSUMASA; NAWA, YASUNORI; FUJITA, SATOSHI
To: SYSMEX CORPORATION; OSAKA UNIVERSITY; NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY
Reel/Frame 062242/0897 →
Priority Claims (2)
JP 2021-035593 · Mar 5, 2021 · national
JP 2021-035597 · Mar 5, 2021 · national
Continuity (1)
Related Publication 20220283154A1 · Sep 8, 2022
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