Ultrasensitive SERS Detection of Five β‑Blockers Achieved Using Chemometrics with a Two-Dimensional Substrate Formed by Large-Sized Ag@SiO2 Nanoparticles

We report on a surface-enhanced Raman scattering (SERS) platform for the detection of five beta-blockers (β-blockers): atenolol, esmolol, labetalol, sotalol, and propranolol. Key to this platform was a two-dimensional substrate formed by self-assembling large Ag@SiO2 nanoparticles (Ag@SiO2 NPs) on a...

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Published inAnalytical chemistry (Washington) Vol. 96; no. 41; pp. 16379 - 16386
Main Authors Cheng, Tao, Xie, Ziyue, Wang, Tianrun, Jiang, Yuning, Guo, Xiaoyu, Liu, Xinling, Wen, Ying, Yang, Haifeng, Wu, Yiping
Format Journal Article
LanguageEnglish
Published Washington American Chemical Society 15.10.2024
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Summary:We report on a surface-enhanced Raman scattering (SERS) platform for the detection of five beta-blockers (β-blockers): atenolol, esmolol, labetalol, sotalol, and propranolol. Key to this platform was a two-dimensional substrate formed by self-assembling large Ag@SiO2 nanoparticles (Ag@SiO2 NPs) on a silicon wafer. The close arrangement of these large nanoparticles on the surface generated a strong and uniform electromagnetic field, which enhanced SERS signal intensity for the detection of small amounts of the target molecules. The intensities of characteristic peaks of the five β-blocker drugs increased linearly with the increase of their concentrations in the range of 10–5 to 10–8 mol/L. The detection limits were 10–10 mol/L for propranolol, 10–9 mol/L for atenolol, labetalol, and sotalol, and 10–8 mol/L for esmolol. Determination of these five β-blocker drugs added to human urine samples, using a portable Raman spectroscopy instrument, showed quantitative recovery (93–101%). Principal component analysis (PCA) and hierarchical cluster analysis (HCA) of SERS spectral data improved the differentiation among these five β-blockers. This study highlights the potential of the developed SERS platform for rapid, on-site detection of illicit drugs and for antidoping screening.
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ISSN:0003-2700
1520-6882
1520-6882
DOI:10.1021/acs.analchem.4c03793