A robust electrochemical immunosensor based on hydroxyl pillar[5]arene@AuNPs@g-C3N4 hybrid nanomaterial for ultrasensitive detection of prostate specific antigen

被引:89
|
作者
Zhou, Xu [1 ,2 ]
Yang, Long [1 ,3 ]
Tan, Xiaoping [3 ]
Zhao, Genfu [1 ]
Xie, Xiaoguang [2 ]
Du, Guanben [1 ]
机构
[1] Southwest Forestry Univ, Sch Mat Sci & Engn, Yunnan Prov Key Lab Wood Adhes & Glued Prod,Minis, Key Lab Forest Resources Conservat & Utilizat Sou, Kunming 650224, Yunnan, Peoples R China
[2] Yunnan Univ, Sch Chem Sci & Technol, Kunming 650091, Yunnan, Peoples R China
[3] Yangtze Normal Univ, Sch Chem & Chem Engn, Chongqing Municipal Educ Commiss, Key Lab Inorgan Special Funct Mat, Chongqing 408100, Peoples R China
关键词
Immunosensor; Pillar[5]arene; Graphitic carbon nitride; Hybrid nanomaterial; Prostate specific antigen; HOST-GUEST INTERACTION; CORE-SHELL NANOPARTICLES; SENSITIVE DETECTION; QUANTUM DOTS; PHOTOCATALYTIC ACTIVITY; MOLECULAR RECOGNITION; GOLD NANOPARTICLES; HYDROGEN-PEROXIDE; SENSING PLATFORM; CANCER BIOMARKER;
D O I
10.1016/j.bios.2018.04.036
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Prostate specific antigen (PSA) is the most significant biomarker for the screening of prostate cancer in human serum. However, most methods for the detection of PSA often require major laboratories, precisely analytical instruments and complicated operations. Currently, the design and development of satisfying electrochemical biosensors based on biomimetic materials (e.g. synthetic receptors) and nanotechnology is highly desired. Thus, we focused on the combination of molecular recognition and versatile nanomaterials in electrochemical devices for advancing their analytical performance and robustness. Herein, by using the present prepared multifunctional hydroxyl pillar[5]arene@gold nanoparticles@graphitic carbon nitride (HP5@AuNPs@g-C3N4) hybrid nanomaterial as robust biomimetic element, a high-performance electrochemical immunosensor for detection of PSA was constructed. The as-prepared immunosensor, with typically competitive advantages of low cost, simple preparation and fast detection, exhibited remarkable robustness, ultra-sensitivity, excellent selectivity and reproducibility. The limit of detection (LOD) and linear range were 0.12 pg mL(-1) (S/N = 3) and 0.0005-10.00 ng respectively. The satisfying results provide a promising approach for clinical detection of PSA in human serum.
引用
收藏
页码:31 / 39
页数:9
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