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适体在碳纤维微电极上的通用共价接枝策略及其用于活体多巴胺的选择性测定

Universal Covalent Grafting Strategy of an Aptamer on a Carbon Fiber Microelectrode for Selective Determination of Dopamine In Vivo.

机构信息

School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an 710061, P. R. China.

出版信息

Anal Chem. 2024 Jun 25;96(25):10322-10331. doi: 10.1021/acs.analchem.4c01167. Epub 2024 May 27.

DOI:10.1021/acs.analchem.4c01167
PMID:38801718
Abstract

The chemical information on brain science provided by electrochemical sensors is critical for understanding brain chemistry during physiological and pathological processes. A major challenge is the selectivity of electrochemical sensors in vivo. This work developed a universal covalent grafting strategy of an aptamer on a carbon fiber microelectrode (CFE) for selective determination of dopamine in vivo. The universal strategy was proposed by oxidizing poly(tannic acid) (pTA) to form an oxidized state (pTA) and then coupling a nucleophilic sulfhydryl molecule of the dopamine-binding mercapto-aptamer with the o-quinone moiety of pTA based on click chemistry for the interfacial functionalization of the CFE surface. It was found that the universal strategy proposed could efficiently graft the aptamer on a glassy carbon electrode, which was verified by using electroactive 6-(ferrocenyl) hexanethiol as a redox reporter. The amperometric method using a fabricated aptasensor for the determination of dopamine was developed. The linear range of the aptasensor for the determination of dopamine was 0.2-20 μM with a sensitivity of 0.09 nA/μM and a limit of detection of 88 nM (S/N = 3). The developed method has high selectivity originating from the specific recognition of the aptamer in concert with the cation-selective action of pTA and could be easily applicable to probe dopamine dynamics in the brain. Furthermore, complex vesicle fusion modes were first observed at the animal level. This work demonstrated that the covalently grafted immobilization strategy proposed is promising and could be extended to the in vivo analysis of other neurochemicals.

摘要

电化学传感器提供的脑科学化学信息对于理解生理和病理过程中的脑化学至关重要。一个主要的挑战是电化学传感器在体内的选择性。本工作开发了一种将适体共价接枝到碳纤维微电极(CFE)上的通用策略,用于体内选择性测定多巴胺。该通用策略是通过将聚(没食子酸)(pTA)氧化形成氧化态(pTA),然后基于点击化学将多巴胺结合的巯基适体的亲核巯基与 pTA 的邻醌部分偶联,从而提出了通用策略,用于 CFE 表面的界面功能化。结果发现,该通用策略可以有效地将适体接枝到玻碳电极上,这可以通过使用电化学活性 6-(二茂铁基)己硫醇作为氧化还原报告分子来验证。使用制备的适体传感器建立了用于测定多巴胺的安培法。该适体传感器用于测定多巴胺的线性范围为 0.2-20 μM,灵敏度为 0.09 nA/μM,检测限为 88 nM(S/N = 3)。该方法具有高选择性,源于适体的特异性识别以及 pTA 的阳离子选择性作用,并且可以很容易地应用于探测大脑中的多巴胺动力学。此外,在动物水平上首次观察到复杂的囊泡融合模式。这项工作表明,所提出的共价接枝固定化策略具有很大的应用前景,并可扩展到其他神经化学物质的体内分析。

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