Nitronyl nitroxide monoradical TEMPO as new electrochemical label for ultrasensitive detection of nucleic acids

被引:18
作者
Wang, Chen [1 ]
Liu, Jingliang [2 ]
Kong, Jinming [1 ]
Zhang, Xueji [3 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Environm & Biol Engn, Nanjing 210094, Peoples R China
[2] Nanjing XiaoZhuang Univ, Sch Environm Sci, Nanjing 211171, Peoples R China
[3] Shenzhen Univ, Hlth Sci Ctr, Sch Biomed Engn, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical biosensor; Nitronyl nitroxide; Stable free radical; New electrochemical label; Nucleic acids detection; AEROBIC OXIDATIVE CONVERSION; ORGANIC ELECTROSYNTHESIS; DNA BIOSENSOR; ALDEHYDES; ELECTRODE; POLYMERIZATION; PYRROLE; SENSORS;
D O I
10.1016/j.aca.2020.08.035
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, a novel electrochemical biosensor based on nitronyl nitroxide monoradical 2,2,6,6-tetramethylpiperidine 1-Oxyl (TEMPO) as new electrochemical label for facile nucleic acids detection is developed. This fast and convenient functional microelectrode was designed by fixing the capture probe peptide nucleic acid (PNA) and using the coordination interaction of Zr4+ with both phosphate groups and carboxyl groups. Differential pulse voltammetry (DPV) was used to study the oxidation current of TEMPO which was combined with the electrode surface and labeled. TEMPO electrochemical signal related to target deoxyribonucleic acid (tDNA) concentration was finally detected when tDNA was added on the surface of glassy carbon electrode (GCE). The detection principle, optimization of key factors and performance analysis of the biosensor are also discussed. A great linear relation is acquired within the scope of 10 pMe100 nM under optimal conditions and the detection limit of this experiment is calculated as low as 2.57 pM (R-2 = 0.996). In addition, complex serum samples were used to explore the practical application of this experiment. The results show the developed electrochemical DNA biosensor has wide application prospects in nucleic acids detection and clinical analysis. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 24
页数:6
相关论文
共 33 条
[1]   Synthetic applications of nonmetal catalysts for homogeneous oxidations [J].
Adam, W ;
Saha-Möller, CR ;
Ganeshpure, PA .
CHEMICAL REVIEWS, 2001, 101 (11) :3499-3548
[2]  
ANELLI PL, 1987, J ORG CHEM, V52, P2559
[3]   TEMPO-mediated oxidation of polysaccharides: survey of methods and applications [J].
Bragd, PL ;
van Bekkum, H ;
Besemer, AC .
TOPICS IN CATALYSIS, 2004, 27 (1-4) :49-66
[4]   A Mild TEMPO-Catalyzed Aerobic Oxidative Conversion of Aldehydes into Nitriles [J].
Fang, Chaojie ;
Li, Meichao ;
Hu, Xinquan ;
Mo, Weimin ;
Hu, Baoxiang ;
Sun, Nan ;
Jin, Liqun ;
Shen, Zhenlu .
ADVANCED SYNTHESIS & CATALYSIS, 2016, 358 (07) :1157-1163
[5]   Electrochemical detection of oligonucleotide by attaching redox probes onto its backbone [J].
Fang, Cheng ;
Ji, Hongmiao ;
Karen, Wang Yanping ;
Rafei, Siti Rafeah Mohamed .
BIOSENSORS & BIOELECTRONICS, 2011, 26 (05) :2670-2674
[6]   DNA Electrochemistry and Electrochemical Sensors for Nucleic Acids [J].
Ferapontova, Elena E. .
ANNUAL REVIEW OF ANALYTICAL CHEMISTRY, VOL 11, 2018, 11 :197-218
[7]   Recent progress in electrochemical sensors and assays for DNA damage and repair [J].
Fojta, Miroslav ;
Danhel, Ales ;
Havran, Ludek ;
Vyskocil, Vlastimil .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2016, 79 :160-167
[8]   Redox catalysis in organic electrosynthesis: basic principles and recent developments [J].
Francke, Robert ;
Little, R. Daniel .
CHEMICAL SOCIETY REVIEWS, 2014, 43 (08) :2492-2521
[9]   Organic electrosynthesis: a promising green methodology in organic chemistry [J].
Frontana-Uribe, Bernardo A. ;
Little, R. Daniel ;
Ibanez, Jorge G. ;
Palma, Agustin ;
Vasquez-Medrano, Ruben .
GREEN CHEMISTRY, 2010, 12 (12) :2099-2119
[10]   NITROXIDE FREE RADICALS - SPIN LABELS FOR PROBING BIOMOLECULAR STRUCTURE [J].
GRIFFITH, OH ;
WAGGONER, AS .
ACCOUNTS OF CHEMICAL RESEARCH, 1969, 2 (01) :17-&