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双-1,2,3-三氮唑配体的合成与表征及其相应铜配合物用于电化学亲和生物传感器的开发。

Synthesis and Characterization of Bis-1,2,3-Triazole Ligand and its Corresponding Copper Complex for the Development of Electrochemical Affinity Biosensors.

机构信息

Biocapteurs-Analyses-Environnement, Université de Perpignan Via Domitia, 66860, Perpignan, France.

Laboratoire de Biodiversité et Biotechnologies Microbiennes, USR 3579 Sorbonne Universités (UPMC) Paris 6 et CNRS Observatoire Océanologique, F-66650, Banyuls-sur-Mer, France.

出版信息

Chemistry. 2021 Jul 2;27(37):9580-9588. doi: 10.1002/chem.202100250. Epub 2021 May 19.

Abstract

The bis-triazole ligand and its corresponding copper complexes were synthesized and characterized for the first time and proposed as new labels for the development of electrochemical aptasensors. The bis-triazole ligand was prepared from methyl 1,6-heptadiyne-4-carboxylate and 2-(azidomethyl)phenol using classical CuAAC in presence of different copper salts. The X-ray structure of bis-triazole showed a symmetry center (C1). UV-Vis and X-band EPR spectra showed that the coordination capacity of the bis-triazole ligand was improved in the presence of triethylamine due to deprotonation of the triazole and phenolate moieties. After complexation with copper, the obtained complex was successfully attached to an anti-estradiol aptamer through thiol-maleimide coupling, and the resulting labelled aptamer was immobilized on a carbon screen-printed electrode by carbodiimide coupling. The electrochemical response of the resulting sensor was shown to decrease in the presence of estradiol, demonstrating that the developed complexes can be applied for the development of aptasensors.

摘要

首次合成并表征了双三唑配体及其相应的铜配合物,并将其提议作为开发电化学适体传感器的新型标记物。双三唑配体是由甲基 1,6-庚二炔-4-羧酸酯和 2-(叠氮甲基)苯酚在不同铜盐存在下使用经典的 CuAAC 制备的。双三唑的 X 射线结构显示出一个对称中心 (C1)。紫外-可见和 X 波段电子顺磁共振光谱表明,由于三唑和酚盐部分的去质子化,三乙胺的存在提高了双三唑配体的配位能力。与铜配位后,所得配合物通过巯基-马来酰亚胺偶联成功连接到抗雌二醇适体上,所得标记适体通过碳二亚胺偶联固定在碳丝网印刷电极上。结果表明,在存在雌二醇的情况下,所得传感器的电化学响应降低,表明所开发的配合物可用于适体传感器的开发。

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