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基于抗氧化剂抑制多巴胺在石墨烯量子点上聚合的荧光开启法测定抗氧化剂。

Turn-on fluorescent assay for antioxidants based on their inhibiting polymerization of dopamine on graphene quantum dots.

机构信息

College of Chemistry and Chemical Engineering, Qufu Normal University, Qufu City, Shandong Province 273165, China.

College of Chemistry and Chemical Engineering, Qufu Normal University, Qufu City, Shandong Province 273165, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2020 Jan 15;225:117516. doi: 10.1016/j.saa.2019.117516. Epub 2019 Sep 6.

Abstract

We describe a sensitive turn-on fluorescent assay for antioxidants by using fluorescence-tunable graphene quantum dots (GQDs). GQDs exhibited strong fluorescence without dopamine (DA). DA could self-polymerize to a thin polydopamine (PDA) film on the surface of GQDs under alkaline environment, resulting in the fluorescence quenching of GQDs via fluorescence resonance energy transfer (FRET). However, the self-polymerization of DA could be effectively inhibited in the presence of antioxidants including glutathione (GSH), ascorbic acid (AA), cysteine (Cys), and homocysteine (Hcys). Thus, the fluorescence of GQDs restored. The "turn-on" sensing of antioxidants could be achieved with high sensitivity. The detection limit for GSH, AA, Cys, and Hcys could be achieved as low as 2.4 nM, 1.5 nM, 4.2 nM, and 4.4 nM, respectively. Finally, the GQDs@PDA system was applied for monitoring cerebral antioxidants in rat brain microdialysates. This work promises new opportunities to evaluate antioxidant capacity in physiological and pathological fields.

摘要

我们描述了一种使用荧光可调石墨烯量子点 (GQDs) 检测抗氧化剂的灵敏开启荧光分析方法。GQDs 在没有多巴胺 (DA) 的情况下表现出强荧光。在碱性环境下,DA 可以在 GQDs 表面自聚合形成一层薄的聚多巴胺 (PDA) 膜,通过荧光共振能量转移 (FRET) 导致 GQDs 的荧光猝灭。然而,在存在抗氧化剂包括谷胱甘肽 (GSH)、抗坏血酸 (AA)、半胱氨酸 (Cys) 和同型半胱氨酸 (Hcys) 的情况下,DA 的自聚合可以被有效抑制。因此,GQDs 的荧光恢复。可以实现对抗氧化剂的“开启”感应,具有很高的灵敏度。GSH、AA、Cys 和 Hcys 的检测限低至 2.4 nM、1.5 nM、4.2 nM 和 4.4 nM。最后,将 GQDs@PDA 系统应用于监测大鼠脑微透析液中的脑内抗氧化剂。这项工作为评估生理和病理领域的抗氧化能力提供了新的机会。

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