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基于电沉积金纳米粒子和磁性微粒子作为生物亲和平台的超灵敏微流控免疫传感器用于牛毛样品中克伦特罗的测定。

Ultra sensitive microfluidic immunosensor for determination of clenbuterol in bovine hair samples using electrodeposited gold nanoparticles and magnetic micro particles as bio-affinity platform.

机构信息

INQUISAL, Departamento de Química, Universidad Nacional de San Luis, CONICET, Chacabuco 917, D5700BWS,San Luis, Argentina.

出版信息

Biosens Bioelectron. 2013 Mar 15;41:211-7. doi: 10.1016/j.bios.2012.08.020. Epub 2012 Aug 17.

Abstract

In this article, we report the first integrated microfluidic immunosensor coupled to a screen-printed carbon electrode (SPCE) applied to determination of clenbuterol (CLB) in bovine hair samples. CLB is a member of the β(2)-agonist drugs which is used in animal production and is banned in Argentine and the European Union. It represents a potential risk and has to be carefully monitored to avoid the illegal use of high amounts of this compound that could result in human food poisoning. In order to perform the CLB detection, the SPCE was modified by gold nanoparticles (AuNPs) electrodeposition. Quantitative determination of CLB was carried out using a competitive indirect immunoassay, method based on the use of anti-CLB antibodies immobilized on magnetic micro particles. The CLB present in bovine hair samples competes immunologically with alkaline phosphatase (AP) enzyme-labeled CLB conjugate for the anti-CLB specific antibodies. Later, p-aminophenyl phosphate was converted to p-aminophenol by AP, and the electroactive product was quantified on AuNPs/SPCE at +0.1 V. The limit of detection for electrochemical method was 0.008 ng mL(-1) and the intra- and inter-assay coefficients of variation were below 6%. This being a veterinary control tool very useful for rapid, sensitive and selective detection of CLB in an "in vitro" technique.

摘要

本文报道了首例将微流控免疫传感器与丝网印刷碳电极(SPCE)集成应用于牛毛样品中克伦特罗(CLB)测定的研究。CLB 是β(2)-激动剂药物的成员之一,用于动物生产,在阿根廷和欧盟被禁用。它代表了一种潜在的风险,必须进行仔细监测,以避免非法使用大量的这种化合物,这可能导致人类食物中毒。为了进行 CLB 检测,SPCE 通过金纳米粒子(AuNPs)的电沉积进行修饰。使用固定在磁性微粒子上的抗 CLB 抗体进行竞争性间接免疫测定,定量测定 CLB。牛毛样品中的 CLB 与碱性磷酸酶(AP)酶标记的 CLB 结合物在免疫学上竞争抗 CLB 特异性抗体。随后,AP 将 p-氨基苯磷酸盐转化为 p-氨基酚,电活性产物在 AuNPs/SPCE 上于+0.1 V 处进行定量。电化学方法的检出限为 0.008ng mL(-1),内和间分析变异系数均低于 6%。这是一种兽医控制工具,非常适合快速、灵敏和选择性地检测“体外”技术中的 CLB。

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