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基于分子印迹聚合物的固相萃取结合基于分子印迹聚合物的传感器用于尿酸检测。

Molecularly imprinted polymer-based solid-phase extraction combined with molecularly imprinted polymer-based sensor for detection of uric acid.

作者信息

Prasad Bhim Bali, Sharma Piyush Sindhu, Lakshmi Dhana

机构信息

Analytical Division, Department of Chemistry, Faculty of Science, Banaras Hindu University, Varanasi 221005, India.

出版信息

J Chromatogr A. 2007 Nov 30;1173(1-2):18-26. doi: 10.1016/j.chroma.2007.10.024. Epub 2007 Oct 13.

DOI:10.1016/j.chroma.2007.10.024
PMID:17977549
Abstract

The development of an easy-to-use, rapid, robust and inexpensive technique is required which can measure the basal concentration of uric acid (UA) lower than 1.0 x 10(-7)M ( approximately 0.017 mgL(-1)) in biological samples to attend the problem of hypouricemia. In the present work an artificial receptor for UA, silica gel-bonded molecularly imprinted polymer (MIP), was used as a sorbent for molecularly imprinted solid-phase extraction (MISPE) in column chromatography. The use of a sensor based on a MIP-modified hanging mercury drop electrode (HMDE), as reported from our laboratory, could estimate UA with detection limit as low as 0.024 mgL(-1) under the optimized conditions of differential pulse, cathodic stripping voltammetric (DPCSV) measurement. However, in the current investigation, with the use of the combination of MISPE followed by detection with a MIP-based HMDE sensor, the minimum detectable concentration could go down to 0.0008 mgL(-1) (RSD=0.63%, S/N=3). The same MIP receptor for both MISPE and the corresponding sensor was able to enhance the preconcentration of analyte substantially so as to attain the desired level of sensitivity; and that to without any interference (cross-reactivity) from other structurally related analogues including the major interferent like ascorbic acid prevalent in the aqueous environment of biological samples.

摘要

需要开发一种易于使用、快速、稳健且廉价的技术,该技术能够测量生物样品中低于1.0×10⁻⁷M(约0.017mgL⁻¹)的尿酸(UA)基础浓度,以解决低尿酸血症问题。在本工作中,一种用于UA的人工受体,硅胶键合分子印迹聚合物(MIP),被用作柱色谱中分子印迹固相萃取(MISPE)的吸附剂。如我们实验室所报道的,使用基于MIP修饰悬汞滴电极(HMDE)的传感器,在差分脉冲阴极溶出伏安法(DPCSV)测量的优化条件下,可估计UA,检测限低至0.024mgL⁻¹。然而,在当前研究中,通过使用MISPE结合基于MIP的HMDE传感器进行检测,最低可检测浓度可降至0.0008mgL⁻¹(相对标准偏差=0.63%,信噪比=3)。用于MISPE和相应传感器的相同MIP受体能够显著提高分析物的预富集程度,从而达到所需的灵敏度水平;并且不会受到其他结构相关类似物的任何干扰(交叉反应),包括生物样品水性环境中普遍存在的主要干扰物如抗坏血酸。

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引用本文的文献

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Molecular Imprinting Technology for Determination of Uric Acid.分子印迹技术测定尿酸。
Int J Mol Sci. 2021 May 10;22(9):5032. doi: 10.3390/ijms22095032.