| Literature DB >> 29149994 |
Zhengyi Qu1, Weidan Na1, Xiaotong Liu1, Hua Liu1, Xingguang Su2.
Abstract
In this paper, we developed a sensitive fluorescence biosensor for tyrosinase (TYR) and acid phosphatase (ACP) activity detection based on nitrogen-doped graphene quantum dots (N-GQDs). Tyrosine could be catalyzed by TYR to generate dopaquinone, which could efficiently quench the fluorescence of N-GQDs, and the degree of fluorescence quenching of N-GQDs was proportional to the concentration of TYR. In the presence of ACP, l-Ascorbic acid-2-phosphate (AAP) was hydrolyzed to generate ascorbic acid (AA), and dopaquinone was reduced to l-dopa, resulting in the fluorescence recovery of the quenched fluorescence by dopaquinone. Thus, a novel fluorescence biosensor for the detection of TYR and ACP activity based on N-GQDs was constructed. Under the optimized experimental conditions, the fluorescence intensity was linearly correlated with the concentration of TYR and ACP in the range of 0.43-3.85 U mL-1 and 0.04-0.7 mU mL-1 with a detection limit of 0.15 U mL-1 and 0.014 mU mL-1, respectively. The feasibility of the proposed biosensor in real samples assay was also studied and satisfactory results were obtained.Entities:
Keywords: Acid phosphatase; Fluorescence biosensor; Graphene quantum dots; Tyrosinase
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Year: 2017 PMID: 29149994 DOI: 10.1016/j.aca.2017.10.010
Source DB: PubMed Journal: Anal Chim Acta ISSN: 0003-2670 Impact factor: 6.558