抗坏血酸
化学
费斯特共振能量转移
荧光
检出限
纳米颗粒
选择性
水解
色谱法
核化学
组合化学
生物化学
纳米技术
催化作用
量子力学
物理
食品科学
材料科学
作者
Heng Zhang,Zhen Wang,Xiaoqing Yang,Zilong Li,Linhao Sun,Jimei Ma,Hong Jiang
标识
DOI:10.1016/j.aca.2019.07.014
摘要
A sensitive nanocomplex probe prepared from fluorescent polydopamine nanoparticles (F-PDA) and cobalt oxyhydroxide (CoOOH) nanosheets was established for the determination of α-glucosidase activity. In this detection system, the fluorescence of F-PDA was firstly quenched by CoOOH nanosheets based on fluorescence resonance energy transfer (FRET). Subsequently, ascorbic acid was produced from 2-O-α-d-glucopyranosyl-l-ascorbic acid which was selectively hydrolyzed by α-glucosidase. CoOOH was reduced to Co2+ by the released ascorbic acid, which resulted in the recovery of F-PDA nanoparticles fluorescence. In consequence, α-glucosidase activity was determined by the fluorescence recovery degree of the F-PDA nanoparticle. This fluorescent method showed a good linear relationship with the activity of α-glucosidase from 2 to 80 U L−1 and low detection limit of 1.65 U L−1 (S/N = 3). This fluorescence probe with high selectivity and sensitivity demonstrated a remarkable applicability in human serum samples and provided an alternative for α-glucosidase inhibitors screening in the discovery of anti-diabetes drugs.
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