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基于半胱氨酸保护的金纳米簇过氧化物酶样活性的柠檬酸比色法生物标志物用于前列腺癌早期检测的纸传感器

A colorimetric paper sensor for citrate as biomarker for early stage detection of prostate cancer based on peroxidase-like activity of cysteine-capped gold nanoclusters.

机构信息

Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.

School of Chemical Engineering, College of Engineering, University of Tehran, Tehran, Iran.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2019 Mar 5;210:251-259. doi: 10.1016/j.saa.2018.11.026. Epub 2018 Nov 15.

Abstract

Citrate is currently considered a preferred biomarker for the early stage detection of prostate cancer. In the present work, based on the highly efficient catalytic properties of gold nanoclusters, a novel system for optical determination of citrate was successfully established under optimized conditions. Cysteine-capped gold nanoclusters (Cys-AuNCs) are shown to have an intrinsic peroxidase-mimetic activity. In the presence of HO Cys-AuNCs nanostructures are able to catalyse the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) with high efficiency to produce a blue dye (with an absorbance maximum at 650 nm). Citrate has carboxylic and hydroxyl groups that can bind with free amino and free carboxyl cysteine groups via hydrogen bonds, thus creating a coating on the surface of the gold nanocluster and inhibiting the cluster oxidation activity. Accordingly, a visual, sensitive and simple colorimetric method using Cys-AuNCs as peroxidase mimetic was developed for detecting citrate. A suitable linear relationship for citrate was obtained for the range of 0.5 to 1000 μM. The limit of detection (LOD) of the proposed method was calculated as 0.1 μM and the relative standard deviation (RSD) was obtained to be less than 4.0%. Moreover, the biosensor was used to perform a paper assay on a Y-shaped microfluidic device and make use of the distinctive features of microchannels such as short response time, very low reagent volume required, low fabrication cost etc. A detection limit of 0.4 μM was achieved through the paper test and a good linear range was observed between 1.0 μM-10 mM. The proposed method was further applied to citrate detection in the human urine sample.

摘要

柠檬酸盐目前被认为是前列腺癌早期检测的首选生物标志物。在本工作中,基于金纳米簇的高效催化特性,在优化条件下成功建立了一种用于光学测定柠檬酸盐的新体系。半胱氨酸封端的金纳米簇(Cys-AuNCs)具有内在的过氧化物酶模拟活性。在 HO 的存在下,Cys-AuNCs 纳米结构能够高效地催化 3,3',5,5'-四甲基联苯胺(TMB)的氧化,生成蓝色染料(在 650nm 处有最大吸收)。柠檬酸盐具有羧基和羟基,可通过氢键与游离氨基和游离羧基半胱氨酸结合,从而在金纳米簇表面形成涂层并抑制簇的氧化活性。因此,开发了一种使用 Cys-AuNCs 作为过氧化物酶模拟物的可视化、灵敏且简单的比色法来检测柠檬酸盐。在 0.5 至 1000μM 的范围内获得了柠檬酸盐的合适线性关系。该方法的检测限(LOD)计算为 0.1μM,相对标准偏差(RSD)小于 4.0%。此外,该生物传感器用于在 Y 型微流控装置上进行纸张分析,并利用微通道的独特特征,如短响应时间、所需试剂体积非常小、制造成本低等。通过纸试验实现了 0.4μM 的检测限,并且观察到 1.0μM-10mM 之间有良好的线性范围。该方法进一步应用于人尿样中柠檬酸盐的检测。

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