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Tytuł pozycji:

A Dual-Modal Single-Antibody Plasmonic Spectro-Immunoassay for Detection of Small Molecules.

Tytuł:
A Dual-Modal Single-Antibody Plasmonic Spectro-Immunoassay for Detection of Small Molecules.
Autorzy:
Zheng P; Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, USA.
Wu L; Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, USA.
Raj P; Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, USA.
Mizutani T; Beckman Coulter Diagnostics - Immunoassay Business Unit, 1000 Lake Hazeltine Dr, Chaska, MN, 55318.
Szabo M; Beckman Coulter Diagnostics - Immunoassay Business Unit, 1000 Lake Hazeltine Dr, Chaska, MN, 55318.
Hanson WA; Beckman Coulter Diagnostics - Immunoassay Business Unit, 1000 Lake Hazeltine Dr, Chaska, MN, 55318.
Barman I; Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, USA.; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.; The Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.
Źródło:
Small (Weinheim an der Bergstrasse, Germany) [Small] 2022 May; Vol. 18 (18), pp. e2200090. Date of Electronic Publication: 2022 Apr 03.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Original Publication: Weinheim, Germany : Wiley-VCH, c2005-
MeSH Terms:
Gold*
Metal Nanoparticles*
Antibodies ; Immunoassay ; Spectrum Analysis, Raman
References:
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Grant Information:
DP2 GM128198 United States GM NIGMS NIH HHS; P41 EB015871 United States EB NIBIB NIH HHS; 2-P41-EB015871-31 United States EB NIBIB NIH HHS; DP2GM128198 United States GM NIGMS NIH HHS
Contributed Indexing:
Keywords: frequency shifts; gold nanopyramid arrays; nanoprobes; plasmonics; spectro-immunoassays; surface enhanced Raman scattering (SERS)
Substance Nomenclature:
0 (Antibodies)
7440-57-5 (Gold)
Entry Date(s):
Date Created: 20220404 Date Completed: 20220506 Latest Revision: 20230502
Update Code:
20240105
PubMed Central ID:
PMC9302383
DOI:
10.1002/smll.202200090
PMID:
35373504
Czasopismo naukowe
Small molecules play a pivotal role in regulating physiological processes and serve as biomarkers to uncover pathological conditions and the effects of therapeutic treatments. However, it remains a significant challenge to detect small molecules given the size as compared to macromolecules. Recently, the newly emerging plasmonic immunoassays based on surface-enhanced Raman scattering (SERS) offer great promise to deliver extraordinary sensitivity. Nevertheless, they are limited by the intrinsic SERS intensity fluctuations associated with the SERS uncertainty principle. The single transducer that relies on the intensity change is also prone to false signals. Additionally, the prevailing sandwich immunoassay format proves less effective towards detecting small molecules. To circumvent these critical issues, a dual-modal single-antibody approach that synergizes both the intensity and shift of the peak-based immunoassay with Raman enhancement, coined as the INSPIRE assay, is developed for small molecules detection. With two independent transduction mechanisms, it allows better prediction of analyte concentration and attenuation of signal artifacts, providing a new and robust strategy for molecular analysis. With a proof-of-concept demonstration for detection of free T4 and testosterone in serum matrix, the authors envision that the INSPIRE assay could be expanded for a wide spectrum of applications in biomedical diagnosis, discovery of new biopharmaceuticals, food safety, and environmental monitoring.
(© 2022 The Authors. Small published by Wiley-VCH GmbH.)

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