Highly sensitive and selective sensor for sunset yellow based on molecularly imprinted polydopamine-coated multi-walled carbon nanotubes

被引:112
|
作者
Yin, Zheng-Zhi [1 ]
Cheng, Shu-Wen [1 ]
Xu, Li-Bin [1 ,2 ]
Liu, Hong-Ying [4 ,5 ]
Huang, Kai [6 ]
Li, Lei [1 ]
Zhai, Yun-Yun [1 ]
Zeng, Yan-Bo [1 ]
Liu, Hai-Qing [1 ]
Shao, Yong [3 ]
Zhang, Zu-Lei [1 ]
Lu, Yi-Xia [1 ]
机构
[1] Jiaxing Univ, Coll Biol Chem Sci & Engn, Jiaxing 314001, Zhejiang, Peoples R China
[2] Changzhou Univ, Coll Petrochem Engn, Changzhou 213614, Peoples R China
[3] Zhejiang Normal Univ, Inst Phys Chem, Jinhua 321004, Zhejiang, Peoples R China
[4] Hangzhou Dianzi Univ, Coll Life Informat Sci & Instrument Engn, Hangzhou 310018, Zhejiang, Peoples R China
[5] Nanjing Univ, Sch Chem & Chem Engn, Nanjing 210093, Jiangsu, Peoples R China
[6] Univ Massachusetts, Sch Med, Worcester, MA 01605 USA
来源
基金
中国国家自然科学基金;
关键词
Molecularly imprinted polymer; Polydopamine; Multi-walled carbon nanotubes; Sunset yellow; Electrochemical sensor; POLYMER; FOOD; NANOPARTICLES; ELECTRODE;
D O I
10.1016/j.bios.2017.10.010
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Polydopamine (PDA) can be formed by monomeric self-polymerization in water. This convenient behavior was exploited to prepare a molecularly imprinted polymer (MIP) layer on the surface of multi-walled carbon nanotubes (MWCNTs) with sunset yellow (SY) as a template molecule. The prepared nanocomposites were characterized, and their electrochemical behavior towards SY was investigated. Under the optimized conditions, a glassy carbon electrode modified with the imprinted nanocomposite showed a highly selective and ultrasensitive electrochemical response to SY compared with the performance of control electrodes and previously reported electrochemical sensors for SY. The improved behavior of the developed sensor can be attributed to its superficial highly matched imprinted cavities on the excellent electrocatalytic matrix of MWCNTs and the electronic barrier of the non-imprinted PDA to outside molecules. The fabricated sensor expressed a linear relationship to SY concentrations from 2.2 nM to 4.64 M with a detection limit of 1.4 nM (S/N = 3). The sensor also exhibited excellent selectivity for SY over its structural analogs, good stability, and adequate reproducibility. The prepared sensor was successfully used to detect SY in real spiked samples. This methodology has potential application value and may be readily adapted to design other PDA-based MIP sensors.
引用
收藏
页码:565 / 570
页数:6
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