Evidence map›Paper›PMID 38874823›Full record

ArticleJournal of fluorescence2025

Detection of Tyrosinase Activity and Inhibitor Validation Based on N-GQDs Fluorescence Sensor.

Jiaxin Li, Hui Guo, Weiwei Ji, Hanqi Chen, Fengju Zhao, Wei Yang, Lili Guo, Junqing Qian

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Article in Journal of fluorescence, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Jiaxin LiCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
Hui GuoCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China. tggh635@163.com.
Weiwei JiCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
Hanqi ChenCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
Fengju ZhaoCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
Wei YangCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
Lili GuoCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
Junqing QianCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tyrosinase inhibitors have the ability to resist melanin formation and can be used for clinical and cosmetic, so it is becoming extremely crucial to search a rapid and effective method for detecting t the activity of tyrosinase. In this study, a sensing probe based on Nitrogen-doped graphene quantum dots (N-GQDs) were prepared with carbamide and citric acid. Tyrosinase can oxidize dopamine to dopamine quinone, which can quench the fluorescence of N-GQDs based on the principle of fluorescence resonance energy transfer (FRET) process, and then the detection of tyrosinase activity can be achieved. The result demonstrated that the fluorescence intensity of N-GQDs was a linear correlation with the activity of tyrosinase. Wide detection linear ranges between 0.05 and 5 U/mL and high selectivity. The detection range of tyrosinase was 0.05 to 5 U/mL and LOD of 0.005 U/mL. According to the above, the fluorescence method established in this work could be successfully used for the trace analysis of tyrosinase and it was verified that KA is an inhibitor of tyrosinase.

Indexed as

Enzyme InhibitorsFluorescent DyesGraphiteMonophenol MonooxygenaseNitrogenQuantum DotsFluorescenceFluorescence Resonance Energy TransferLimit of DetectionSpectrometry, FluorescenceEnzyme InhibitorsFluorescent DyesGraphiteMonophenol MonooxygenaseNitrogenFluorescence probeInhibitorNitrogen-doped graphene quantum dotsTyrosinase

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.