Reduced graphene oxide-functionalized FeOOH for signal-on photoelectrochemical sensing of prostate-specific antigen with bioresponsive controlled release system

被引:74
作者
Zhou, Qian [1 ]
Lin, Youxiu [1 ]
Shu, Jian [1 ]
Zhang, Kangyao [1 ]
Yu, Zhenzhong [1 ]
Tang, Dianping [1 ]
机构
[1] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Collaborat Innovat Ctr Detect Technol Haixi Food, Key Lab Analyt Sci Food Safety & Biol,Dept Chem, Fuzhou 350116, Fujian, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
Photoelectrochemical sensor; Bioresponsive controllable release; Iron oxyhydroxide; Reduced graphene oxide; Prostate specific antigen; CHARGE SEPARATION; ALPHA-FEOOH; IMMUNOASSAY; PERFORMANCE; NANOCOMPOSITE; PHOTOCATALYST; PLATFORM; NANOPARTICLES; PRECIPITATION; AMPLIFICATION;
D O I
10.1016/j.bios.2017.06.033
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A new and signal-on photoelectrochemical (PEC) sensing platform was successfully designed for the sensitive detection of prostate-specific antigen (PSA), using reduced graphene oxide- functionalized iron oxyhydroxide (FeOOH-rGO) as the photoactive material, accompanying target-responsive controlled release system to achieve the signal amplification. Introduction of rGO as electron mediator greatly facilitated the electron transfer from FeOOH to electrode under visible light, which inhibited the electron-hole recombination to enhance the photo-activity of FeOOH-rGO. Additionally, the bioresponsive release system was controlled via the reaction of target PSA with the aptamer capped glucose-loading mesoporous silica nanoparticle (MSN) to release numerous glucose molecules (as the electron donors) for the amplification of the photocurrent generated from FeOOHrGO. Thus, more glucose molecules could be released and enhanced photocurrents could be obtained with the increasing PSA concentrations. Experimental results showed that the photocurrents of the PEC sensing platform were linearly dependent on the logarithm of PSA concentrations from 1.0 pg/mL to 100 ng/mL. Moreover, the PEC sensing system afforded good stability and specificity, and its accuracy matched well with the commercial PSA enzyme-linked immunosorbent assay (ELISA) kit. The excellent performance of the PEC sensing platform indicated its promising prospect as a useful tool for PSA detection in practical application.
引用
收藏
页码:15 / 21
页数:7
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