Electron Transfer Mediated Electrochemical Biosensor for MicroRNAs Detection Based on Metal Ion Functionalized Titanium Phosphate Nanospheres at Attomole Level

被引:93
作者
Cheng, Fang-Fang [1 ]
He, Ting-Ting [1 ,2 ]
Miao, Hai-Tiao [1 ]
Shi, Jian-Jun [1 ,2 ]
Jiang, Li-Ping [1 ]
Zhu, Jun-Jie [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
[2] Anhui Univ Sci & Technol, Sch Chem Engn, Huainan 232001, Peoples R China
基金
中国国家自然科学基金;
关键词
microRNAs; titanium phosphate; electron transfer; electrochemical biosensor; ROLLING-CIRCLE AMPLIFICATION; LABEL-FREE; ISOTHERMAL AMPLIFICATION; SENSITIVE DETECTION; MOLECULAR BEACON; GOLD ELECTRODES; HAIRPIN-PROBE; DNA; NANOPARTICLES; DNAZYME;
D O I
10.1021/am508690x
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
MicroRNAs (miRNAs) have emerged as new candidates as diagnostic and prognostic biomarkers for the detection of a wide variety of cancers; thus, sensitive and selective detection of microRNAs is significant for early-phase cancer diagnosis and disease prevention. A novel and simple electrochemical miRNA biosensor was developed using Cd2+-modified titanium phosphate nanoparticles as signal unit, two DNA as capture probes, and Ru(NH3)(63)(+) as electron transfer mediator. Large quantities of cadmium ions were mounted in titanium phosphate spheres to output the electrochemical signal. Because of the presence of Ru(NH3)(63)(+) molecules that interacted with DNA base-pairs as electron wire, the electrochemical signal significantly increased more than 5 times. This approach achieved a wide dynamic linear range from 1.0 aM to 10.0 pM with an ultralow limit detection of 0.76 aM, exerting a substantial enhancement in sensitivity. Moreover, the proposed biosensor was sufficiently selective to discriminate the target miRNAs from homologous miRNAs and could be used for rapid and direct analysis of miRNAs in human serum. Therefore, this strategy provides a new and ultrasensitive platform for miRNA expression profiling in biomedical research and clinical diagnosis.
引用
收藏
页码:2979 / 2985
页数:7
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