Block-Polymer-Restricted Sub-nanometer Pt Nanoclusters Nanozyme-Enhanced Immunoassay for Monitoring of Cardiac Troponin I

被引:132
作者
Chen, Shuyun [1 ]
Yu, Zhichao [1 ]
Wang, Yunsen [1 ]
Tang, Juan [3 ]
Zeng, Yongyi [2 ]
Liu, Xiaolong [2 ]
Tang, Dianping [1 ]
机构
[1] Fuzhou Univ, Dept Chem, Key Lab Analyt Sci Food Safety & Biol MOE & Fujia, Fuzhou 350108, Peoples R China
[2] Fujian Med Univ, Mengchao Hepatobiliary Hosp, United Innovat Mengchao Hepatobiliary Technol Key, Fuzhou 350025, Peoples R China
[3] Jiangxi Normal Univ, Dept Chem & Chem Engn, Key Lab Green Chem Jiangxi Prov, Nanchang 330022, Peoples R China
基金
中国国家自然科学基金;
关键词
REDUCTION;
D O I
10.1021/acs.analchem.3c03249
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Noble-metal nanozymes have demonstrated great potential in various fields. However, aggregation of single-particle nanoparticles severely affects their exposed catalytically active sites to the extent of exhibiting weak enzyme-like activity. Here, we present an organic block surfactant (polyvinylpyrrolidone, PVP) to construct monodisperse water-stable Pt nanoclusters (Pt NCs) for an enhanced immunoassay of cardiac troponin I (cTnI). The PVP-modified Pt NC nanozyme exhibited up to 16.3 U mg(-1) peroxidase-mimicking activity, which was mainly attributed to the ligand modification on the surface and the electron-absorbing effect of the ligand on the Pt NCs. The PVP-modified Pt NCs have a lower OH-transition potential, as determined by density functional theory. Under optimized experimental conditions, the enhanced nanozyme immunoassay strategy exhibited an ultrawide dynamic response range of 0.005-50 ng mL(-1) for cTnI targets with a detection limit of 1.3 pg mL(-1), far superior to some reported test protocols. This work provides a designable pathway for the design of artificial enzymes with high enzyme-like activity to further expand the practical range of enzyme alternatives.
引用
收藏
页码:14494 / 14501
页数:8
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