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一种使用纸质基底和多元曲线分辨法测定尿酸的便携式表面增强拉曼光谱方法。

A portable SERS method for the determination of uric acid using a paper-based substrate and multivariate curve resolution.

作者信息

Villa Javier E L, Poppi Ronei J

机构信息

Institute of Chemistry, University of Campinas, P.O. Box 6154, 13081-970 Campinas, SP, Brazil.

出版信息

Analyst. 2016 Mar 21;141(6):1966-72. doi: 10.1039/c5an02398j.

Abstract

This paper presents a portable quantitative method for the on-site determination of uric acid in urine using surface-enhanced Raman spectroscopy (SERS) and gold nanoparticle-coated paper as a substrate. A procedure was developed for the rapid preparation of cost-effective SERS substrates that enabled the adequate control of a homogeneous active area and the use of small quantities of gold nanoparticles per substrate. The standard addition method and multivariate curve resolution-alternating least squares (MCR-ALS) were applied to compensate for the matrix effect and to address overlapping bands between uric acid and interference SERS spectra. The proposed methodology demonstrated better performance than conventional univariate methods (in terms of linearity, accuracy and precision), a wide linear range (0-3.5 mmol L(-1)) and an adequate limit of detection (0.11 mmol L(-1)). For the first time, a portable SERS method coupled with chemometrics was developed for the routine analysis of uric acid at clinically relevant concentrations with minimal sample preparation and easy extension for the on-site determination of other biomarkers in complex sample matrices.

摘要

本文提出了一种便携式定量方法,用于使用表面增强拉曼光谱(SERS)和金纳米颗粒包覆纸作为基底现场测定尿液中的尿酸。开发了一种快速制备具有成本效益的SERS基底的程序,该程序能够充分控制均匀的活性区域,并使每个基底使用少量的金纳米颗粒。应用标准加入法和多元曲线分辨交替最小二乘法(MCR-ALS)来补偿基质效应,并解决尿酸与干扰SERS光谱之间的谱带重叠问题。所提出的方法在性能上优于传统的单变量方法(在线性、准确性和精密度方面),具有较宽的线性范围(0-3.5 mmol L(-1))和适当的检测限(0.11 mmol L(-1))。首次开发了一种结合化学计量学的便携式SERS方法,用于临床相关浓度尿酸的常规分析,样品制备最少,并且易于扩展以现场测定复杂样品基质中的其他生物标志物。

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