Molecularly imprinted electroluminescence switch sensor with a dual recognition effect for determination of ultra-trace levels of cobalt (II)

被引:23
|
作者
Li, Shuhuai [1 ,2 ]
Li, Jianping [3 ]
Ma, Xionghui [1 ,2 ]
Pang, Chaohai [1 ,2 ]
Yin, Guihao [1 ,2 ]
Luo, Jinhui [1 ,2 ]
机构
[1] Chinese Acad Trop Agr Sci, Analysts & Test Ctr, Haikou 571101, Hainan, Peoples R China
[2] Hainan Prov Key Lab Qual & Safety Trop Fruits & V, Haikou 571101, Hainan, Peoples R China
[3] Guilin Univ Technol, Coll Chem & Bioengn, Guilin 541004, Peoples R China
来源
关键词
Molecularly-imprinted; Bovine serum albumin-metal; Dual selective; Switch; Electrochemiluminescence; CARBON QUANTUM DOTS; METAL-IONS; NANOPARTICLES; ELECTROCHEMILUMINESCENCE; AMPLIFICATION;
D O I
10.1016/j.bios.2019.111321
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A dual selection/recognition effect is described for cobalt (II) ions (Co2+). It is based on bovine serum albuminmetal-Co2+ coordination (BSA-Co2+) and the use of a molecularly imprinted polymer (MIP). An electro-chemiluminescence (ECL) switch sensor was designed for detecting nanomolar levels of Co2+. The BSA-Co2+ coordination complex was chosen as a template to prepare a MIP modified switch sensor. The coordination reaction between BSA and Co2+ provides the first step in recognition, and MIP provides the second step for Co2+. This leads to a strong improvement in selectivity of the sensor. A multi-walled carbon nanotube/Cu nanoparticles/carbon quantum dots nanocomposite (MWCNT/Cu/C-dots) acts as an ECL device, and the BSA-Co2+ complex quenches the ECL signal. Therefore, the elution and resorption of BSA Co2+ can be used as a switch to control ECL. Additionally, a method was established to detect Co2+, with the detection limit as low as 3.07 x 10(-10) mol/L. The method was applied to the analysis of spiked environmental water, soil samples, and agricultural products. The recovery rates of the method were in the range of 87.5-111.3%.
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页数:6
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