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采用化学计量学,利用大尺寸 Ag@SiO2 纳米粒子形成的二维基底,实现了对五种β受体阻滞剂的超灵敏 SERS 检测。

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

机构信息

The Education Ministry Key Laboratory of Resource Chemistry, Joint International Research Laboratory of Resource Chemistry, Ministry of Education, Shanghai Key Laboratory of Rare Earth Functional Materials, and Shanghai Frontiers Science Center of Biomimetic Catalysis, College of Chemistry and Materials Science, Shanghai Normal University, Shanghai 200234, China.

出版信息

Anal Chem. 2024 Oct 15;96(41):16379-16386. doi: 10.1021/acs.analchem.4c03793. Epub 2024 Oct 3.

Abstract

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@SiO nanoparticles (Ag@SiO 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 to 10 mol/L. The detection limits were 10 mol/L for propranolol, 10 mol/L for atenolol, labetalol, and sotalol, and 10 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.

摘要

我们报告了一种用于检测五种β受体阻滞剂(β-blockers)的表面增强拉曼散射(SERS)平台:阿替洛尔、艾司洛尔、拉贝洛尔、索他洛尔和普萘洛尔。该平台的关键是由硅片上自组装的大 Ag@SiO 纳米粒子(Ag@SiO NPs)形成的二维基底。这些大纳米粒子在表面上的紧密排列产生了强而均匀的电磁场,增强了 SERS 信号强度,从而可以检测到少量的目标分子。五种β受体阻滞剂药物的特征峰强度随其浓度在 10 到 10 摩尔/升范围内的增加呈线性增加。检测限为 10 摩尔/升的普萘洛尔,10 摩尔/升的阿替洛尔、拉贝洛尔和索他洛尔,以及 10 摩尔/升的艾司洛尔。使用便携式拉曼光谱仪对添加到人尿样中的这五种β受体阻滞剂药物进行测定,显示出定量回收(93-101%)。SERS 光谱数据的主成分分析(PCA)和层次聚类分析(HCA)提高了这五种β受体阻滞剂的区分能力。本研究强调了所开发的 SERS 平台在快速、现场检测非法药物和反兴奋剂筛查方面的潜力。

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