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利用激光诱导荧光光谱法,通过等离子体增强抗体固定化,开发基于毛细管的癌胚抗原免疫传感器。

Plasma-enhanced antibody immobilization for the development of a capillary-based carcinoembryonic antigen immunosensor using laser-induced fluorescence spectroscopy.

机构信息

Research Center of Analytical Instrumentation, Analytical & Testing Centre, College of Chemistry, Sichuan University, Chengdu 610064, P R China.

出版信息

Anal Chem. 2013 May 7;85(9):4578-85. doi: 10.1021/ac400226n. Epub 2013 Apr 18.

DOI:10.1021/ac400226n
PMID:23547735
Abstract

In this study, antibody immobilization using a microwave-induced H2O/Ar plasma pretreatment was achieved for the first time. Plasma was used to activate the surface of a capillary-based immunosensor by increasing the density of silicon hydroxyls and dangling bonds to ensure better silanization. The capture antibodies were covalently immobilized after the silanized surface reacted with glutaraldehyde and antibodies. A Cy3-labeled detection antibody was used in combination with the antigen captured by the immunosensor to complete the sandwich-type immunoassay, and the signals were measured using a laser-induced fluorescence system. Microwave-induced H2O/Ar plasma pretreatment of the carcinoembryonic antigen (CEA) immunosensor improved the antibody immobilization, and there was an obvious improvement in the linear detection range, i.e., 1 order of magnitude compared with a commercial enzyme-linked immunosorbent assay (ELISA). This novel immobilization method dramatically improved the detection limit (0.5 pmol/L CEA) and sensitivity. Assay validation studies indicated that the correlation coefficient reached 0.9978, and the relative standard deviations were <7% for all samples, with recoveries of 99.7-107.1%. Furthermore, the immunosensor was applied successfully to CEA determination in actual saliva specimens with high sensitivity, acceptable precision, and reasonable accuracy. This enhanced CEA immunosensor based on microwave-induced H2O/Ar plasma was demonstrated to be a sensitive tool for CEA diagnostics.

摘要

在这项研究中,首次采用微波诱导 H2O/Ar 等离子体预处理实现抗体固定化。等离子体通过增加硅羟基数和悬空键来激活基于毛细管的免疫传感器表面,以确保更好的硅烷化。硅烷化表面与戊二醛和抗体反应后,将捕获抗体共价固定。使用 Cy3 标记的检测抗体与免疫传感器捕获的抗原结合,完成三明治型免疫分析,并使用激光诱导荧光系统测量信号。微波诱导 H2O/Ar 等离子体预处理癌胚抗原(CEA)免疫传感器改善了抗体固定化,线性检测范围明显提高,即与商业酶联免疫吸附测定(ELISA)相比提高了 1 个数量级。这种新型固定化方法极大地提高了检测限(0.5 pmol/L CEA)和灵敏度。分析验证研究表明,相关系数达到 0.9978,所有样品的相对标准偏差均<7%,回收率为 99.7-107.1%。此外,该免疫传感器成功应用于实际唾液样本中 CEA 的高灵敏度检测,具有可接受的精密度和合理的准确性。基于微波诱导 H2O/Ar 等离子体的增强型 CEA 免疫传感器被证明是 CEA 诊断的敏感工具。

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