Double-enzymes-mediated Fe2+/Fe3+ conversion as magnetic relaxation switch for pesticide residues sensing
Double-enzymes-mediated Fe2+/Fe3+ conversion as magnetic relaxation switch for pesticide residues sensing
复制标题
双酶介导的 Fe2/Fe3 转化作为农药残留传感的磁弛豫开关
DOI:
10.1016/j.jhazmat.2020.123619
复制
发表时间:
2021
影响因子:
13.6
通讯作者:
Chen Yiping
中科院分区:
文献类型:
--
作者:
Wu Long;Zhou Min;Liu Chen;Chen Xiaoqiang;Chen Yiping
It is a great challenge to develop a newly rapid and accurate detection method for pesticide residues. In this work, based on acetylcholinesterase (AChE) and choline oxidase (CHO), a double-enzymes-mediated Fe2+/Fe3+conversion as magnetic relaxation switch was explored for the measurement of acetamiprid residue. In the double-enzymes reactions, acetylcholine chloride (ACh) can be catalyzed to produce choline by AChE, which is successively hydrolyzed to betaine and hydrogen peroxide (H2O2) by CHO. According to the enzyme inhibition principle, AChE activity will be inactivated in the presence of acetamiprid, thus leading to the less production of H2O2. Wherein, Fe2+, ACh, AChE and CHO were optimized as the reaction substrates. In the reaction system, acetamiprid can be reflected by the transverse relaxation time (T2) that related with H2O2mediated Fe2+variations, which was further developed as an enzyme cascade amplification method. The detection linear range is 0.01∼1000 μg mL−1(R2= 0.99), and the limit of detection (LOD) is 2.66 ng mL−1(S/N = 3, n = 3), behaving a 335-fold improvement in LOD than that of traditional enzyme inhibition method (0.89 μg mL−1). This method can realize “one-step mixing” detection of acetamiprid, which makes it a promising analytical tool for monitoring pesticide residue in complicated samples.