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基于多重信号放大策略的强自增效应控释电化学发光生物传感器用于痕量前列腺特异性抗原的检测。

Controlled-Release Electrochemiluminescence Biosensor with Strong Self-On Effect by a Multiple Signal Amplification Strategy for Trace Detection of Prostate-Specific Antigen.

机构信息

School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, P. R. China.

Shandong Water Conservancy Vocational College, Rizhao 276826, P. R. China.

出版信息

Anal Chem. 2024 Apr 30;96(17):6659-6665. doi: 10.1021/acs.analchem.4c00048. Epub 2024 Apr 18.

DOI:10.1021/acs.analchem.4c00048
PMID:38635916
Abstract

The enhancement of sensitivity in biological analysis detection can reduce the probability of false positives of the biosensor. In this work, a novel self-on controlled-release electrochemiluminescence (CRE) biosensor was designed by multiple signal amplification and framework-enhanced stability strategies. As a result, the changes of the ECL signal were enhanced before and after the controlled-release process, achieving sensitive detection of prostate-specific antigen (PSA). Specifically, for one thing, FeO@CeO-NH with two paths for enhancing the generation of coreactant radicals was used as the coreaction accelerator to boost ECL performance. For another, due to the framework stability, zeolitic imidazolate framework-8-NH (ZIF-8-NH) was combined with luminol to make the ECL signal more stable. Based on these strategies, the constructed CRE biosensor showed a strong self-on effect in the presence of PSA and high sensitivity in a series of tests. The detection range and limit of detection (LOD) were 5 fg/mL to 10 ng/mL and 2.8 fg/mL (S/N = 3), respectively, providing a feasible approach for clinical detection of PSA.

摘要

生物分析检测灵敏度的提高可以降低生物传感器假阳性的概率。在这项工作中,通过多重信号放大和框架增强稳定性策略,设计了一种新型的自控释放电化学发光(CRE)生物传感器。结果,在控制释放过程前后,ECL 信号的变化得到增强,实现了对前列腺特异性抗原(PSA)的灵敏检测。具体而言,一方面,使用具有两种增强反应剂自由基生成途径的 FeO@CeO-NH 作为共反应加速剂来提升 ECL 性能。另一方面,由于框架稳定性,沸石咪唑酯骨架-8-NH(ZIF-8-NH)与鲁米诺结合使 ECL 信号更加稳定。基于这些策略,构建的 CRE 生物传感器在存在 PSA 时表现出强烈的自启动效应,并且在一系列测试中具有高灵敏度。检测范围和检测限(LOD)分别为 5 fg/mL 至 10 ng/mL 和 2.8 fg/mL(S/N = 3),为 PSA 的临床检测提供了一种可行的方法。

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