免疫分析
等离子体子
纳米技术
分子
材料科学
对偶(语法数字)
情态动词
化学
光电子学
抗体
生物
高分子化学
有机化学
文学类
艺术
免疫学
作者
Peng Zheng,Lintong Wu,Piyush Raj,Takayuki Mizutani,Miklos Szabo,William A. Hanson,Ishan Barman
出处
期刊:Small
[Wiley]
日期:2022-04-03
卷期号:18 (18)
被引量:18
标识
DOI:10.1002/smll.202200090
摘要
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.
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