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碱性磷酸酶连接光学免疫分析的发展综述

Overview on the Development of Alkaline-Phosphatase-Linked Optical Immunoassays.

作者信息

Liu Lin, Chang Yong, Lou Jiaxin, Zhang Shuo, Yi Xinyao

机构信息

College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, China.

College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.

出版信息

Molecules. 2023 Sep 11;28(18):6565. doi: 10.3390/molecules28186565.

Abstract

The drive to achieve ultrasensitive target detection with exceptional efficiency and accuracy requires the advancement of immunoassays. Optical immunoassays have demonstrated significant potential in clinical diagnosis, food safety, environmental protection, and other fields. Through the innovative and feasible combination of enzyme catalysis and optical immunoassays, notable progress has been made in enhancing analytical performances. Among the kinds of reporter enzymes, alkaline phosphatase (ALP) stands out due to its high catalytic activity, elevated turnover number, and broad substrate specificity, rendering it an excellent candidate for the development of various immunoassays. This review provides a systematic evaluation of the advancements in optical immunoassays by employing ALP as the signal label, encompassing fluorescence, colorimetry, chemiluminescence, and surface-enhanced Raman scattering. Particular emphasis is placed on the fundamental signal amplification strategies employed in ALP-linked immunoassays. Furthermore, this work briefly discusses the proposed solutions and challenges that need to be addressed to further enhance the performances of ALP-linked immunoassays.

摘要

实现具有卓越效率和准确性的超灵敏目标检测,需要免疫分析技术的进步。光学免疫分析在临床诊断、食品安全、环境保护等领域已展现出巨大潜力。通过酶催化与光学免疫分析的创新且可行的结合,在提升分析性能方面已取得显著进展。在各类报告酶中,碱性磷酸酶(ALP)因其高催化活性、高周转数和广泛的底物特异性脱颖而出,使其成为开发各种免疫分析的理想候选者。本综述通过将ALP用作信号标签,对光学免疫分析的进展进行了系统评估,涵盖荧光、比色法、化学发光和表面增强拉曼散射。特别强调了ALP连接免疫分析中采用的基本信号放大策略。此外,这项工作简要讨论了为进一步提高ALP连接免疫分析性能而提出的解决方案和需要解决的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7d/10536125/be816c2cde1e/molecules-28-06565-g017.jpg

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