Photothermal visual sensing of alkaline phosphatase based on the etching of Au@MnO2 core-shell nanoparticles

被引:6
|
作者
Li, Jin [1 ,2 ]
Liu, Xiao-Peng [1 ]
Ye, Wen-Qi [1 ]
Xu, Zhang-Run [1 ]
机构
[1] Northeastern Univ, Res Ctr Analyt Sci, Shenyang 110819, Peoples R China
[2] Shenyang Med Coll, Sch Pharm, Shenyang 110034, Peoples R China
基金
中国国家自然科学基金;
关键词
Alkaline phosphatase; MnO2-coated gold nanoparticles; Etching; Photothermal sensing; GOLD NANOPARTICLES; ASSAY; BIOMARKERS; AGGREGATION; THERMOMETER; THERAPY; CELLS; DOTS;
D O I
10.1016/j.jcis.2023.03.091
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Alkaline phosphatase (ALP), as a crucial enzyme involved in many physiological activities, is always used as one of the significant biomarkers in clinical diagnosis. Herein, a novel, simple, and effective photother-mal quantitative method based on the etching of MnO2-coated gold nanoparticles (Au@MnO2 NPs) was established for ALP activity assay with a household thermometer-based visual readout. The photothermal effect of Au@MnO2 NPs is much higher than that of MnO2 NPs or Au NPs. The MnO2 shell of Au@MnO2 NPs can be etched by ascorbic acid, a product of ALP-catalyzed hydrolysis of 2-phospho-L-ascorbic acid. With the etching of Au@MnO2 NPs, the photothermal conversion efficiency decreased gradually, causing the decrease of the temperature increment of the solutions by degrees. A household thermometer, instead of large-scale and professional instruments, was used as a signal reader to realize the visual quan-titative detection. The photothermal platform was used successfully for the determination of ALP with a wide linear range from 2.0 to 50 U/L and a detection limit as low as 0.75 U/L. Moreover, the inhibition efficiency of sodium vanadate for ALP activity was investigated, proving the photothermal quantitative method will be a potential platform for screening enzyme inhibitors. Such a sensitive, facile, and low-cost sensing assay provides a new prospect to develop platforms for point-of-care testing. (c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:568 / 576
页数:9
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