FRET Effect between Fluorescent Polydopamine Nanoparticles and MnO2 Nanosheets and Its Application for Sensitive Sensing of Alkaline Phosphatase

被引:176
作者
Xiao, Ting [1 ,2 ]
Sun, Jian [1 ]
Zhao, Jiahui [1 ,3 ]
Wang, Shuang [1 ,2 ]
Liu, Guoyong [1 ,2 ]
Yang, Xiurong [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] Univ Sci & Technol China, Hefei 230026, Anhui, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
fluorescent polydopamine nanoparticle; MnO2; nanosheets; Forster resonance energy transfer; alkaline phosphatase; fluorescent probe; COORDINATION POLYMER NANOPARTICLES; POLYNUCLEOTIDE KINASE-ACTIVITY; HUMAN WHOLE-BLOOD; RATIOMETRIC FLUORESCENCE; GOLD NANOPARTICLES; ASCORBIC-ACID; QUANTUM DOTS; ASSAY; CONVERSION; INHIBITION;
D O I
10.1021/acsami.7b18816
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
As an essential and universal hydrolase, alkaline phosphatase (ALP) has been identified as a crucial indicator of various diseases. Herein, we, for the first time, expanded the application of fluorescent polydopamine (F-PDA) nanoparticles to nanoquencher-based biosensing system, as well as discovered the reversible quenching effect of manganese dioxide (MnO2) nano-sheets on the fluorescence of F-PDA nanoparticles and intensively confirmed the quenching mechanism of Forster resonance energy transfer by using transmission electron microscopy, UV-vis, Fourier transform infrared spectroscopy, and fluorescence lifetime experiments. By means of the ALP-triggered generation of ascorbic acid (AA) from the substrate ascorbic acid 2-phosphate, the AA-triggered reduction of MnO2 nanosheets to Mn2+, as well as the clear quenching mechanism of F-PDA nanoparticles by MnO2 nanosheets, we have developed a label-free, low-cost, visual, and facile synthetic fluorescent biosensor for convenient assay of ALP activity. The fluorescent bioassay shows a good linear relationship from 1 to 80 mU/mL (R-2 = 0.999), with a low detection limit of 0.34 mU/mL, and the excellent applicability in human serum samples demonstrates potential applications in clinical diagnosis and biomedical research.
引用
收藏
页码:6560 / 6569
页数:10
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