Evidence map›Paper›PMID 42093873›Full record

ArticleFrontiers in pharmacology2026

A universal fluorescent sensing platform based on "signal switching induced by enzyme catalyzed substrate hydrolysis" for high-throughput discovery of xanthine oxidase inhibitors from traditional Chinese medicine.

Guojing Liu, Kunhui Sun, Sitong Lai, Xiaoyi Liu, Yuanyuan Ge, Ping Wang, Bing Wang, Yuhong Li, Xie-An Yu

Abstract read
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Article in Frontiers in pharmacology, 2026. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Guojing Liu *Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Kunhui Sun *Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Sitong LaiKey Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Xiaoyi LiuKey Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Yuanyuan GeNMPA Center for Innovation and Research in Regulatory Science, Shenzhen Institute for Drug Control, Shenzhen, China.
Ping WangNMPA Center for Innovation and Research in Regulatory Science, Shenzhen Institute for Drug Control, Shenzhen, China.
Bing WangNMPA Center for Innovation and Research in Regulatory Science, Shenzhen Institute for Drug Control, Shenzhen, China.
Yuhong LiKey Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Xie-An YuNMPA Center for Innovation and Research in Regulatory Science, Shenzhen Institute for Drug Control, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Traditional Chinese medicine (TCM) serves as the treasure house for discovering lead compounds in drug development, demonstrating significant potential in the creation of anti-gout agents. However, given the complexity of TCM, conventional detection methods not only were susceptible to interference from metabolites but also suffered from low throughput, thereby hindering the efficient screening of inhibitors. Methods: This study developed a universal fluorescent sensing platform based on the principle of enzyme specific substrate recognition for the high-throughput screening of xanthine oxidase (XOD) inhibitors. Results: This approach offered two advances: (1) Interference-resistant detection: for screening in the complex system of TCM, its high emission wavelength (λem = 690 nm > 680 nm) and larger Stokes shift (Δλ = 148 nm) further enhanced anti-interference capability. (2) High-throughput screening capacity: by integrating HPLC-fully automatic partial fraction collector (HPLC-FC) and UHPLC-Q-TOF/MS, we established an "isolation-detection-identification" platform, screening and identifying four XOD inhibitors (Quercetin-3-sambubioside, Hyperoside, Isoquercitrin and Astragalin) from Nelumbinis Folium (NF) extract, with their combined inhibitory contribution accounting for 61.22% of the total inhibition activity. Discussion: Therefore, this strategy provided a powerful methodological tool for the high-throughput discovery of next-generation XOD inhibitors from TCM. And it offers a universal paradigm for the high-throughput discovery of bioactive metabolites from TCM targeting different diseases.

Indexed as

enzyme catalyzed substrate hydrolysisfluorescent sensing platformhigh-throughput screeningtraditional Chinese medicinexanthine oxidase inhibitor

Identifiers

PMID42093873
PMCPMC13139129

What Socratic holds

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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 Socratic graph.