Cited by 33Chromatography in Natural ProductsTraditional Chinese Medicine AnalysisBioactive natural compounds

Analysis of tyrosinase binders from Glycyrrhiza uralensis root: Evaluation and comparison of tyrosinase immobilized magnetic fishing-HPLC and reverse ultrafiltration-HPLC

Liu, Liangliang, Shi, Shuyun, Chen, Xiaoqing, Peng, Mijun·2013·Journal of Chromatography B

Abstract

Tyrosinase inhibitors play an important role in cosmetic products, food supplements and medicinal industries. In this study, a new facile method based on tyrosinase immobilized magnetic fishing (IMF) coupled with high performance liquid chromatography-diode array detector-tandem mass spectrometry (HPLC-DAD-MS/MS) was developed to screen and identify tyrosinase binders from Glycyrrhiza uralensis root. Experiments were carried out to select optimal immobilization and incubation conditions. The activity of immobilized tyrosinase retained 76.3% after ten consecutive cycles, and remained over 95% when stored at 4°C for about two months. Eleven tyrosinase binders, including original compounds and transformation products were successfully screened and characterized from G. uralensis root, while dihydrodaidzein and pratensein were reported for the first time. Compared with ultrafiltration-HPLC assay, IMF-HPLC displayed many attractive advantages, including convenient solid-liquid separation ability, good stability, high reusability and activity, which indicated that IMF-HPLC had a broad applicability. The results indicated that IMF-HPLC method is a facile, effective and reproductive way to screen and identify active components from complex mixtures.

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Crossref · 10.1016/j.jchromb.2013.06.002

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  • Secondary metabolites of G. uralensis root including liquiritin apioside, neolicuroside, liquiritigenin, licorice saponin G2, chrysoeriol, dihydrodaidzein, formononetin, glycyrrhisoflavanone, glycyrrhizinic acid, licoarylcoumarin, and pratensein inhibit tyrosinase activity.

    “Secondary metabolites of G. uralensis root such as liquiritin apioside, neolicuroside, liquiritigenin, licorice saponin G2, chrysoeriol, dihydrodaidzein, formononetin, glycyrrhisoflavanone, glycyrrhizinic acid, licoarylcoumarin, and pratensein showed the capacity to inhibit tyrosinase activity [45].”

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Authors
Liu, L., Shi, S., Chen, X., & Peng, M.
Affiliations
  • Central South University (CN)
  • Jishou University (CN)
Corresponding author
  • Shi, Shuyun
  • Chen, Xiaoqing
Venue
Journal of Chromatography B
Publisher
Elsevier BV
Published
2013-08
Volume
932
Pages
19-25
ISSN
1570-0232 (ISSN-L)
OpenAlex
W2067664537
Cited by
33
References
0
Citations by year
2026: 1 · 2024: 4 · 2023: 1 · 2022: 3 · 2021: 4 · 2020: 1 · 2019: 4 · 2018: 2 · 2016: 5 · 2015: 3 · 2014: 3 · 2013: 2
FWCI
4.11
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Chromatography B (publishedVersion)
  • PubMed (publishedVersion)
  • Journal of Chromatography A
Topics
  • Physical Sciences › Chemistry › Analytical Chemistry › Chromatography in Natural Products
  • Health Sciences › Medicine › Complementary and alternative medicine › Traditional Chinese Medicine Analysis
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioactive natural compounds
Keywords
tyrosinase inhibitors, dihydrodaidzein, enzyme immobilization, enzyme reusability, degradation intermediates
MeSH terms
Agaricales, Chromatography, High Pressure Liquid, Enzyme Inhibitors, Enzymes, Immobilized, Plant Extracts, Monophenol Monooxygenase, Ultrafiltration, Plant Roots, Glycyrrhiza uralensis, Tandem Mass Spectrometry, Magnetite Nanoparticles

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