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基于鲁米诺功能化、银纳米粒子修饰的氧化石墨烯的黄曲霉毒素 M1 的可视化电致化学发光生物传感

Visual electrochemiluminescence biosensing of aflatoxin M1 based on luminol-functionalized, silver nanoparticle-decorated graphene oxide.

机构信息

Department of Chemistry, University of Isfahan, Isfahan 81746-73441, Iran.

Chemical Injuries Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

出版信息

Biosens Bioelectron. 2018 Feb 15;100:382-388. doi: 10.1016/j.bios.2017.09.035. Epub 2017 Sep 21.

Abstract

A sensitive electrochemiluminescence (ECL) aptasensor for aflatoxin M1 (AFM1) detection by a closed bipolar electrode (BPE) array has been introduced. The thiolated AFM1 aptamer was immobilized on gold nanoparticle-coated magnetic FeO nanoparticles (Apt-GMNPs). Luminol-functionalized silver nanoparticle-decorated graphene oxide (GO-L-AgNPs) participates in π-π interactions with the unpaired bases of the immobilized aptamer (Apt-GMNPs-GO-L-AgNPs). After the Apt-GMNPs-GO-L-AgNPs were introduced to a gold anodic BPE array, the individual electrodes were subjected to different concentrations of AFM1. Upon the interaction of AFM1 with the aptamers, the GO-L-AgNPs detach from the aptamer; the resulting ECL of luminol and HO at the anodic poles is monitored using a photomultiplier tube (PMT) or smartphone, and the images are analyzed using ImageJ software. This process triggers thionine reduction at the cathodic poles. Under the optimal conditions obtained by a face-centered central composite design (FCCD), the PMT-based detection of the BPE-ECL aptasensor exhibit a linear response over a wide dynamic range from 5 to 150ngmL, with a detection limit of 0.01ngmL. Additionally, smartphone-based detection shows a linear relationship between the ECL image gray value and the logarithmic concentration of the AFM1 target over a range of 10-200ngmL, with a detection limit of 0.05ngmL. Furthermore, the BPE-ECL aptasensor was successfully used to detect AFM1 in milk complex media without any serious interferences with reliable reproducibility (average relative standard deviation (RSD = 2.3%)). This smartphone-based detection opens a new horizon for bioanalysis that does not require a trained technician to operate and is a promising technology for point-of-care testing.

摘要

一种基于闭双极电极(BPE)阵列的用于检测黄曲霉毒素 M1(AFM1)的灵敏电化学发光(ECL)适体传感器已经被提出。巯基化的 AFM1 适体被固定在金纳米粒子涂覆的磁性 FeO 纳米粒子(Apt-GMNPs)上。发光氨功能化的银纳米粒子修饰的氧化石墨烯(GO-L-AgNPs)与固定化适体(Apt-GMNPs-GO-L-AgNPs)的未配对碱基发生π-π相互作用。将 Apt-GMNPs-GO-L-AgNPs 引入到金阳极 BPE 阵列后,各个电极都被施加了不同浓度的 AFM1。当 AFM1 与适体相互作用时,GO-L-AgNPs 从适体上脱离;发光氨和 HO 在阳极的 ECL 反应被光电倍增管(PMT)或智能手机监测,并使用 ImageJ 软件对图像进行分析。这个过程触发了阴极上的硫堇还原。在面心立方中心复合设计(FCCD)得到的最佳条件下,基于 PMT 的 BPE-ECL 适体传感器的检测在 5 至 150ngmL 的宽动态范围内呈现出线性响应,检测限为 0.01ngmL。此外,基于智能手机的检测显示,在 10-200ngmL 的范围内,ECL 图像灰度值与 AFM1 目标物的对数浓度之间存在线性关系,检测限为 0.05ngmL。此外,该 BPE-ECL 适体传感器还成功地用于检测牛奶复杂介质中的 AFM1,没有任何严重的干扰,具有可靠的重现性(平均相对标准偏差(RSD=2.3%))。这种基于智能手机的检测为生物分析开辟了一个新的领域,不需要经过培训的技术人员进行操作,是一种有前途的即时检测技术。

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