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碳纳米线交错电极表面的电流-电压生物传感“胱抑素C”:腹主动脉瘤的临床标志物分析

Current-Volt Biosensing "Cystatin C" on Carbon Nanowired Interdigitated Electrode Surface: A Clinical Marker Analysis for Bulged Aorta.

作者信息

Chen Xi, Kang Jie, Sun Qiu, Liu Cheng, Wang Hongling, Wang Chen, Gopinath Subash C B

机构信息

Department of Vascular Surgery, Wuhan No.1 Hospital, WuHan, HuBei 430022, China.

Department of Vascular Surgery, Liaocheng People's Hospital, Liaocheng, Shandong Province 252000, China.

出版信息

J Anal Methods Chem. 2022 May 23;2022:8160502. doi: 10.1155/2022/8160502. eCollection 2022.

Abstract

A carbon nanowire-modified surface with interdigitated electrode (IDE) sensing system was introduced to identify abdominal aortic aneurysm biomarker "papain," also known as cysteine protease, used as the capture probe to identify Cystatin C. Papain was immobilized through the covalent integration of amine group on papain and the carboxyl group with carbon nanowire. This papain-modified electrode surface was utilized to detect the different concentrations of Cystatin C (100 pg/mL to 3.2 ng/mL). The interaction between papain and Cystatin C was monitored using a picoammeter, and the response curves were compared. With increasing Cystatin C concentrations, the total current levels were gradually increased with a linear range from 200 pg/mL to 3.2 ng/mL, and the current differences were plotted and the detection limit of Cystatin C was calculated as 200 pg/mL. The averaging of three independent experiments ( = ) was made with 3 estimation, and the determination coefficient was  = 1.8477 × 0.7303 and  = 0.9878. Furthermore, control experiments with creatinine and gliadin failed to bind the immobilized papain, indicating the specific detection of Cystatin C.

摘要

引入了一种具有叉指电极(IDE)传感系统的碳纳米线修饰表面,用于识别腹主动脉瘤生物标志物“木瓜蛋白酶”(也称为半胱氨酸蛋白酶),将其用作捕获探针来识别胱抑素C。木瓜蛋白酶通过其胺基与碳纳米线上的羧基共价整合而固定化。利用这种木瓜蛋白酶修饰的电极表面检测不同浓度的胱抑素C(100 pg/mL至3.2 ng/mL)。使用皮安计监测木瓜蛋白酶与胱抑素C之间的相互作用,并比较响应曲线。随着胱抑素C浓度的增加,总电流水平逐渐升高,线性范围为200 pg/mL至3.2 ng/mL,绘制电流差异并计算胱抑素C的检测限为200 pg/mL。进行了三次独立实验的平均值( = )并进行了3次估计,测定系数为 = 1.8477×0.7303且 = 0.9878。此外,用肌酐和麦醇溶蛋白进行的对照实验未能与固定化的木瓜蛋白酶结合,表明对胱抑素C具有特异性检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67a0/9152415/ea0d65a93463/JAMC2022-8160502.001.jpg

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