Laser induced graphene electrochemical aptasensor based on tetrahedral DNA for ultrasensitive on-site detection of microcystin-LR

被引:16
|
作者
Wang, Yuan [1 ]
Li, Yuye [1 ]
Liu, Chang [1 ]
Dong, Na [1 ]
Liu, Dong [1 ]
You, Tianyan [1 ]
机构
[1] Jiangsu Univ, Sch Agr Engn, Key Lab Modern Agr Equipment & Technol, Minist Educ, Zhenjiang 212013, Jiangsu, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Microcystin-LR; Laser induced graphene; Electrochemical aptasensor; Tetrahedron DNA; On site detection; IMMUNOSENSOR;
D O I
10.1016/j.bios.2023.115610
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The development of accurate and reliable sensor for on-site detection of microcystin-LR (MC-LR), one of hazardous environmental pollutants, is highly required. Herein, a laser induced graphene (LIG)-based electrochemical aptasensor for sensitive on-site detection of MC-LR was reported. LIG electrode, the substrate of aptasensor, was prepared via thermal transfer with ethylene-vinyl acetate copolymer, and LIG acted as quasireference electrode to replace conventional Ag/AgCl electrode for better operability and robustness. LIG electrode provided large surface area to assemble tetrahedral DNA to absorb methylene blue (MB) for the signal amplification. For detection, the specific recognition of MC-LR with aptamer led to the stripping of tetrahedral DNA complex and further the decreased redox current of MB (IMB). Consequently, the fabricated aptasensor offered high analytical performance for MC-LR detection with a linear range of 1 x 10-2-1 x 105 pM and a detection limit of 3 x 10-3 pM, which was successfully used for water sample analysis with comparable reliability and accuracy of standard method. Furthermore, a portable detection platform by coupling of LIG-based electrochemical aptasensor with electrochemical workstation was constructed for on-site detection of MC-LR. This work offers a novel method for the on-site monitoring of MC-LR, which promotes the investigation of LIG-based electrochemical biosensing in the field of environmental analysis.
引用
收藏
页数:8
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