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表面受限的 CuInS@ZnS 纳米晶体的低触发潜力电致化学发光及其生物传感应用。

Low-Triggering-Potential Electrochemiluminescence from Surface-Confined CuInS@ZnS Nanocrystals and their Biosensing Applications.

机构信息

School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.

出版信息

Anal Chem. 2021 Sep 14;93(36):12250-12256. doi: 10.1021/acs.analchem.1c01601. Epub 2021 Aug 31.

Abstract

Electrochemiluminescence (ECL) of low triggering potential is strongly anticipated for ECL assays with less inherent electrochemical interference and improved long-term stability of the working electrode. Herein, effects of the thiol capping agents and the states of luminophores, i.e., the thiol-capped CuInS@ZnS nanocrystals (CuInS@ZnS-Thiol), on the ECL triggering potential of CuInS@ZnS-Thiol/NH·HO were explored on the Au working electrode. The thiol capping agent of glutathione (GSH) not only enabled CuInS@ZnS-Thiol/NH·HO with the stronger oxidative-reduction ECL than other thiol capping agents but also demonstrated the largest shift for the ECL triggering potential of CuInS@ZnS-Thiol/NH·HO upon changing the luminophores from the monodispersed state to the surface-confined state. CuInS@ZnS-GSH/NH·HO exhibited an efficient oxidative-reduction ECL around 0.78 V (vs Ag/AgCl) with CuInS@ZnS-GSH of the monodispersed state. Upon employing CuInS@ZnS-GSH as the ECL tag and immobilizing them onto the Au working electrode, the oxidative-reduction ECL of CuInS@ZnS-GSH/NH·HO was lowered to 0.32 V (vs Ag/AgCl), which was about 0.88 V lower than that of traditional Ru(bpy)/TPrA (typically ∼1.2 V, vs Ag/AgCl). The ECL of the CuInS@ZnS-GSH/NH·HO system with the luminophore of both monodispersed and surface-confined states was spectrally identical to each other, indicating that this surface-confining strategy exhibited negligible effect on the excited state for the ECL of CuInS@ZnS-GSH. A surface-confined ECL sensor around 0.32 V was fabricated with CuInS@ZnS-GSH as a luminophore, which could sensitively and selectively determine the K-RAS gene from 1 to 500 pM with a limit of detection at 0.5 pmol L (S/N = 3).

摘要

电化学发光(ECL)的低触发电位对于 ECL 分析非常重要,因为它可以减少电化学干扰,并提高工作电极的长期稳定性。本文中,我们探索了巯基封端剂的作用以及发光体的状态(即巯基封端的 CuInS@ZnS 纳米晶(CuInS@ZnS-Thiol))对 Au 工作电极上的 CuInS@ZnS-Thiol/NH·HO 的 ECL 触发电位的影响。谷胱甘肽(GSH)的巯基封端剂不仅使 CuInS@ZnS-Thiol/NH·HO 具有比其他巯基封端剂更强的氧化还原 ECL,而且当将发光体从单分散状态变为表面受限状态时,CuInS@ZnS-Thiol/NH·HO 的 ECL 触发电位也发生了最大的变化。CuInS@ZnS-GSH/NH·HO 在 0.78 V(相对于 Ag/AgCl)附近表现出有效的氧化还原 ECL,此时 CuInS@ZnS-GSH 为单分散状态。当使用 CuInS@ZnS-GSH 作为 ECL 标记并将其固定在 Au 工作电极上时,CuInS@ZnS-GSH/NH·HO 的氧化还原 ECL 降低至 0.32 V(相对于 Ag/AgCl),比传统的 Ru(bpy)/TPrA(通常约 1.2 V,相对于 Ag/AgCl)低约 0.88 V。具有单分散和表面受限状态的发光体的 CuInS@ZnS-GSH/NH·HO 系统的 ECL 在光谱上彼此相同,这表明这种表面限制策略对 CuInS@ZnS-GSH 的 ECL 激发态几乎没有影响。以 CuInS@ZnS-GSH 为发光体,制备了一种约 0.32 V 的表面受限 ECL 传感器,该传感器可对 1 至 500 pM 的 K-RAS 基因进行灵敏且选择性的检测,检测限为 0.5 pmol L(S/N = 3)。

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