IP Library › Granted Patent US 11,261,475
Granted Patent B2
US 11,261,475 · App. 16/311,161 · Granted Mar 1, 2022

Nano-neurotoxicity bio-marker composition based on intracellular aggregates which are biomarkers of degenerative brain diseases

Inventors: Tae Hwan Shin (Daegu, KR); Geetika Phukan (Suwon-si, KR); Man Jeong Paik (Seoul, KR); Hyeon-Seong Lee (Incheon, KR); Hyung-Jin Park (Suwon-si, KR); Da Yeon Lee (Ulsan, KR); Gwang Lee (Suwon-si, KR)
C12Q1/025C12Q1/6837C12Q1/6881C12Q1/6883C12Q2600/106C12Q2600/112C12Q2600/142C12Q2600/156C12Q2600/158C12Q2600/16
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Quick Facts
Patent No.
US 11,261,475
App. No.
16/311,161
Granted
Mar 1, 2022
Kind
B2
Abstract

A method of assessing neurotoxicity of nanoparticles, includes: preparing a tissue or cell sample of mammal exposed to the nanoparticles; analyzing at least one polyamine metabolite selected from the group consisting of putrescine, N1-acetylspermidine, N8-acetylspermidine, N1-acetylspermine and spermine in the sample; and comparing expression degree of the polyamine metabolite with that of a control.

Claims (14)

1. A method of assessing neurotoxicity of nanoparticles comprising:

preparing a tissue or cell sample of mammal;

treating the tissue or cell sample with the nanoparticles;

analyzing polyamine metabolites including putrescine, N1-acetylspermidine, N8-acetylspermidine, N1-acetylspermine and spermine in the sample;

comparing an amount of the polyamine metabolites with that of a control; and

determining the neurotoxicity of nanoparticles of the sample, if:

an amount of the putrescine is increased at least twice compared to the control not treated with the nanoparticles; and

an amount of the N1-acetylspermidine, the N8-acetylspermidine, the N1-acetylspermine and the spermine is decreased less than ½ times compared to the control not treated with the nanoparticles.

2. The method of assessing neurotoxicity of nanoparticles of claim 1 , further comprising:

analyzing at least one gene selected from the group consisting of ornithine decarboxylase 1 (ODC1), spermidine/spermine N1 acetyltransferase 1 (SAT1), polyamine oxidase (PAOX) and spermidine synthase 1 (SRM1) in the sample, wherein the at least one gene is involved in polyamine metabolism; and

comparing expression degree of the gene with that of a control.

3. The method of assessing neurotoxicity of nanoparticles of claim 2 ,

wherein the sample is exposed to the nanoparticles if an expression of the ODC1 gene, the SAT1 gene, the PAOX gene and the SRM1 gene is increased compared to the control not treated with the nanoparticles.

4. The method of assessing neurotoxicity of nanoparticles of claim 1 , wherein the nanoparticles are MNPs@SiO 2 (RITC) particles.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2018
From: SHIN, TAE HWAN; PHUKAN, GEETIKA; PAIK, MAN JEONG; LEE, HYEON-SEONG; PARK, HYUNG-JIN; LEE, DA YEON; LEE, GWANG
To: AJOU UNIVERSITY INDUSTRY-ACADEMIC COOPERATION FOUNDATION
Reel/Frame 047811/0960 →
Priority Claims (1)
KR 10-2016-0076570 · Jun 20, 2016 · national
Continuity (1)
Related Publication 20190194715A1 · Jun 27, 2019