Integrated Solid-State Nanopore Electrochemistry Array for Sensitive, Specific, and Label-Free Biodetection

被引:20
作者
Li, Xinchun [1 ,2 ]
Zhang, Tianchi [1 ]
Gao, Pengcheng [3 ]
Wei, Benmei [1 ]
Jia, Yongmei [1 ]
Cheng, Yong [1 ]
Lou, Xiaoding [3 ]
Xia, Fan [1 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Hubei Key Lab Bioinorgan Chem & Materia Med, 1037 Luoyu Rd, Wuhan 430074, Hubei, Peoples R China
[2] Guangxi Med Univ, Sch Pharm, Pharmacuet Anal Div, 22 Shuangyong Rd, Nanning 530021, Peoples R China
[3] China Univ Geosci, Fac Mat Sci & Chem, Minist Educ, Engn Res Ctr Nanogeomat, 388 Lumo Rd, Wuhan 430074, Hubei, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金; 中国博士后科学基金;
关键词
SEQUENCE-SPECIFIC DETECTION; SINGLE-MOLECULE ANALYSIS; CHRONOCOULOMETRIC DNA; NANOCHANNEL ARRAY; BIOSENSOR; MICRORNAS; SENSOR; ASSAY; GATEKEEPERS; RECOGNITION;
D O I
10.1021/acs.langmuir.8b02010
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanopore ionic current measurement is currently a prevailing readout and offers considerable opportunities for bioassays. Extending conventional electrochemistry to nanoscale space, albeit noteworthy, remains challenging. Here, we report a versatile electrochemistry array established on a nanofluidic platform by controllably depositing gold layers on the two outer sides of anodic aluminum oxide (AAO) nanopores, leading to form an electrochemical microdevice capable of performing amperometry in a label-free manner. Electroactive species ferricyanide ions passing through gold-decorated nanopores act as electrochemical indicator to generate electrolytic current signal. The electroactive species flux that dominates current signal response is closely related to the nanopore permeability. Such well-characteristic electrolytic current-species flux correlation lays a premise for quantitative electrochemical analysis. As a proof-of-concept demonstration, we preliminarily verify the analytical utility by detection of nucleic acid and protein at picomolar concentration levels. Universal surface modification and molecule assembly, specific target recognition and reliable signal output in nanopore enable direct electrochemical detection of biomolecules without the need of cumbersome probe labeling and signal amplification.
引用
收藏
页码:14787 / 14795
页数:9
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