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Dual signal amplification coupling dual inhibition effect for fabricating photoelectrochemical chlorpyrifos biosensor

Journal 2016 · IF 4.758 · 发表于 2016 年 7 月 16 日
作者: Hanping Mao,Yuting Yan,Nan Hao,Qian Liu,Jing Qian,Saibo Chen,Kun Wang
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摘要

Photoelectrochemical (PEC) detection is an attractive analytical tool as it allows for an elegant and sensitive assay. However, designing a novel detection strategy to achieve an excellent PEC analytical performance is still highly challenging. Herein we design a novel photoelectrochemical (PEC) chlorpyrifos biosensor based on dual signal amplification strategy coupling dual inhibition effect. Dual signal amplification strategy was achieved by coupling the graphene quantum dots sensitized CuFe 2 O 4 magnetic nanocrystal clusters (GQDs–CuFe 2 O 4 MNCs) with the amplification of enzymolysis products. In this biosensing architecture, the GQDs–CuFe 2 O 4 MNCs prepared by electrostatic adsorption showed nearly 4-fold and 30-fold enhancement photocurrent compared with the pure CuFe 2 O 4 MNCs and GQDs, respectively. And the contact angle measurement demonstrated that the GQDs–CuFe 2 O 4 MNCs exhibited good biocompatibility . Based on all these above advantages, the GQDs–CuFe 2 O 4 MNCs were immobilized on the magnetic electrode surface by a fast and simple magnetism-assisted assembly, and the acetylcholinesterase (AChE) was further coated on the surface of the as-prepared multifunctional electrode. Due to thiocholine (enzymolysis products) acts as a sacrificial electron donor to scavenge the holes, compared with the GQDs–CuFe 2 O 4 MNCs modified electrode in the acetylthiocholine chloride solution, the photocurrent of the resulting AChE-based biosensor was further significantly enhanced. Based on the dual inhibition of AChE activity by chlorpyrifos and the formation of Cu-chlorpyrifos complex hindered the electron transfer of CuFe 2 O 4 MNCs toward the electrode surface , the proposed AChE-based biosensor can be applied to the quantification of chlorpyrifos with a linear range from 0.001   μg   mL −1 to 1   μg   mL −1 and a detection limit of 0.3   ng   mL −1 (S/N   =   3). This novel dual signal amplification strategy opens up a new avenue for achieving high sensitivity in the field of PEC biosensing.