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基于 Au@Ag NPs 基底耦合表面增强拉曼光谱法的新型痕量毒死蜱波长选择方法的研究。

Development of a novel wavelength selection method for the trace determination of chlorpyrifos on Au@Ag NPs substrate coupled surface-enhanced Raman spectroscopy.

机构信息

School of Food and Biological Engineering, Jiangsu University, Zhenjiang 212013, P.R. China.

出版信息

Analyst. 2019 Feb 11;144(4):1167-1177. doi: 10.1039/c8an02086h.

Abstract

A novel wavelength selection method, namely interval combination population analysis-minimal redundancy maximal relevance (ICPA-mRMR), was employed for the trace level detection of chlorpyrifos (CPS) coupled surface-enhanced Raman spectroscopy (SERS). Herein, a highly sensitive SERS enhancement substrate, Au@Ag nanoparticles (NPs), was synthesized possessing strong enhancement of Raman signals for CPS quantification (enhancement factor: 2.5 × 106). Compared with other established methods such as partial least squares (PLS), synergy interval partial least squares-genetic algorithm (siPLS-GA) and competitive adaptive reweighted sampling-partial least squares (CARS-PLS), ICPA-mRMR yielded the best results with higher correlation coefficients (Rc = 0.9917, RP = 0.9895), ratios of performance to deviation (RPD = 6.8797), and lower root mean square errors (RMSEC = 0.1998, RMSEP = 0.2271). The proposed method was employed for the determination of trace level CPS in tea samples, and the recovery percentages were in the range 90%-108%. Meanwhile, this method was validated using a standard GC-MS method indicating no significant difference (P > 0.05). The proposed methodology offers a rapid, sensitive and powerful analytical platform for the detection of pesticide residues in food.

摘要

一种新的波长选择方法,即区间组合种群分析-最小冗余最大相关性(ICPA-mRMR),被用于检测毒死蜱(CPS)的痕量检测与表面增强拉曼光谱(SERS)的结合。在此,合成了具有高灵敏度的 SERS 增强衬底 Au@Ag 纳米粒子(NPs),对 CPS 的定量分析具有很强的拉曼信号增强作用(增强因子:2.5×106)。与其他已建立的方法(如偏最小二乘法(PLS)、协同区间偏最小二乘法-遗传算法(siPLS-GA)和竞争自适应重加权采样-偏最小二乘法(CARS-PLS)相比,ICPA-mRMR 具有更好的结果,得到了更高的相关系数(Rc=0.9917,RP=0.9895)、性能偏差比(RPD=6.8797)和更低的均方根误差(RMSEC=0.1998,RMSEP=0.2271)。该方法被用于茶叶样品中痕量 CPS 的测定,回收率在 90%-108%之间。同时,该方法还通过标准 GC-MS 方法进行了验证,结果表明没有显著差异(P>0.05)。该方法为食品中农药残留的检测提供了一种快速、灵敏、强大的分析平台。

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