Back to Search Start Over

Charge Transfer Platform and Catalytic Amplification of Phenanthroimidazole Derivative: A New Strategy for DNA Bases Recognition

Authors :
Lu, Nannan
Liu, He
Huang, Rui
Gu, Yue
Yan, Xiaoyi
Zhang, Tingting
Xu, Zhiqian
Xu, Haixin
Xing, Yue
Song, Yu
Li, Xuwen
Zhang, Zhiquan
Source :
Analytical Chemistry; September 2019, Vol. 91 Issue: 18 p11938-11945, 8p
Publication Year :
2019

Abstract

Research about DNA composition has been concentrated on DNA damage in the past few decades. However, it still remains a great challenge to construct a rapid, facile, and accurate approach for simultaneously monitoring four DNA bases, guanine (G), adenine (A), thymine (T), and cytosine (C). Herein, a novel electrochemical sensor based on phenanthroimidazole derivative, 2-(4-bromophenyl)-1-phenyl-1H-phenanthro[9,10-d]-imidazole (PPI), is successfully fabricated by a simple electrochemical method. The bromophenyl group in PI could expand their aromatic plane, induce the π-conjugated extension, and enhance the charge transfer and π–π interaction. The phenyl group at N1 position could regulate the intermolecular interaction, which could promote the possibility of intermolecular connection. The PPI polymer (poly(PPI)) with π-electron enriched conjugation architecture has been applied in simultaneous determination of G, A, T, and C in neutral solution by square wave voltammetry (SWV) method with well-separated peak potentials at 0.714, 1.004, 1.177, and 1.353 V, respectively. The sensor functionalized with poly(PPI) exhibits wide linear response for G, A, T, and C in the concentration ranges of 3–300, 1–300, 30–800, and 20–750 μM, respectively. With favorable selectivity, stability, and reproducibility, the sensor is successfully utilized to monitor four DNA bases in real samples, displaying a promising prospect for electrochemical sensing devices.

Details

Language :
English
ISSN :
00032700 and 15206882
Volume :
91
Issue :
18
Database :
Supplemental Index
Journal :
Analytical Chemistry
Publication Type :
Periodical
Accession number :
ejs50811335
Full Text :
https://doi.org/10.1021/acs.analchem.9b02746