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基于双链 DNA 和金纳米粒子的用于血清和牛奶中链霉素检测的比色和荧光猝灭适体传感器。

Colorimetric and fluorescence quenching aptasensors for detection of streptomycin in blood serum and milk based on double-stranded DNA and gold nanoparticles.

机构信息

Cardiovascular Research Center, Ghaem hospital, Mashhad University of Medical Sciences, Mashhad, Iran.

Nanotechnology Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran; Research Institute of Sciences and New Technology, Mashhad, Iran.

出版信息

Food Chem. 2016 Jan 1;190:115-121. doi: 10.1016/j.foodchem.2015.05.079. Epub 2015 May 19.

Abstract

Antibiotic residues in animal foodstuffs are of great concern to consumers. In this study, fluorescence quenching and colorimetric aptasensors were designed for detection of streptomycin based on aqueous gold nanoparticles (AuNPs) and double-stranded DNA (dsDNA). In the absence of streptomycin, aptamer/FAM-labeled complementary strand dsDNA is stable, resulting in the aggregation of AuNPs by salt and an obvious color change from red to blue and strong emission of fluorescence. In the presence of streptomycin, aptamer binds to its target and FAM-labeled complementary strand adsorbs on the surface of AuNPs. So the well-dispersed AuNPs remain stable against salt-induced aggregation with a wine-red color and the fluorescence of FAM-labeled complimentary strand is efficiently quenched by AuNPs. The colorimetric and fluorescence quenching aptasensors showed excellent selectivity toward streptomycin with limit of detections as low as 73.1 and 47.6 nM, respectively. The presented aptasensors were successfully used to detect streptomycin in milk and serum.

摘要

动物食品中的抗生素残留令消费者十分关注。本研究基于金纳米粒子(AuNPs)和双链 DNA(dsDNA),设计了用于检测链霉素的荧光猝灭和比色适体传感器。在不存在链霉素的情况下,适体/FAM 标记的互补链 dsDNA 稳定,导致 AuNPs 因盐而聚集,颜色从红色变为蓝色,荧光强度明显增强。当存在链霉素时,适体与靶标结合,FAM 标记的互补链吸附在 AuNPs 表面。因此,分散良好的 AuNPs 在盐诱导的聚集下保持稳定,呈现酒红色,FAM 标记的互补链的荧光被 AuNPs 有效猝灭。比色和荧光猝灭适体传感器对链霉素表现出优异的选择性,检测限分别低至 73.1 和 47.6 nM。该适体传感器成功用于牛奶和血清中链霉素的检测。

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