Key Laboratory for Analytical Science of Food Safety and Biology (Ministry of Education and Fujian Province), Collaborative Innovation Center of Detection Technology for Haixi Food Safety and Products (Fujian Province), State Key Laboratory of Photocatalysis on Energy and Environment, Department of Chemistry, Fuzhou University, Fuzhou 350116, PR China.
Key Laboratory for Analytical Science of Food Safety and Biology (Ministry of Education and Fujian Province), Collaborative Innovation Center of Detection Technology for Haixi Food Safety and Products (Fujian Province), State Key Laboratory of Photocatalysis on Energy and Environment, Department of Chemistry, Fuzhou University, Fuzhou 350116, PR China.
Biosens Bioelectron. 2017 Dec 15;98:15-21. doi: 10.1016/j.bios.2017.06.033. Epub 2017 Jun 16.
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 FeOOH-rGO. 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 1.0pg/mL to 100ng/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.
一个新的、基于信号的光电化学(PEC)传感平台被成功设计用于灵敏检测前列腺特异性抗原(PSA),使用还原氧化石墨烯功能化的氧化铁(FeOOH-rGO)作为光活性材料,伴随目标响应控制释放系统以实现信号放大。引入 rGO 作为电子介体,在可见光下极大地促进了从 FeOOH 到电极的电子转移,抑制了电子-空穴复合,增强了 FeOOH-rGO 的光活性。此外,通过 PSA 与适配体封闭的载葡聚糖介孔硅纳米颗粒(MSN)的反应来控制生物响应释放系统,以释放大量葡萄糖分子(作为电子供体),从而放大 FeOOH-rGO 产生的光电流。因此,随着 PSA 浓度的增加,可以释放更多的葡萄糖分子,并获得增强的光电流。实验结果表明,PEC 传感平台的光电流对数与 PSA 浓度从 1.0pg/mL 到 100ng/mL 呈线性相关。此外,PEC 传感系统具有良好的稳定性和特异性,其准确性与商业 PSA 酶联免疫吸附测定(ELISA)试剂盒相匹配。PEC 传感平台的优异性能表明,它有望成为实际应用中 PSA 检测的有用工具。