Recent advance in the discovery of tyrosinase inhibitors from natural sources via separation methods |
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| Authors: | Xiao-wei Zhang Guang-li Bian Pei-ying Kang Xin-jie Cheng Kai Yan Yong-li Liu Yan-xia Gao De-qiang Li |
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| Institution: | aDepartment of Neurological Surgery, the Second Hospital of Hebei Medical University, Shijiazhuang, China;bDepartment of Pharmacy, the Second Hospital of Hebei Medical University, Shijiazhuang, China;cDepartment of Clinical Laboratory, the Second Hospital of Hebei Medical University, Shijiazhuang, China;dInstitute for Drug Control of Hebei Province, Shijiazhuang, China |
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| Abstract: | Tyrosinase (TYR) inhibitors are in great demand in the food, cosmetic and medical industrials due to their important roles. Therefore, the discovery of high-quality TYR inhibitors is always pursued. Natural products as one of the most important sources of bioactive compounds discovery have been increasingly used for TYR inhibitors screening. However, due to their complex compositions, it is still a great challenge to rapid screening and identification of biologically active components from them. In recent years, with the help of separation technologies and the affinity and intrinsic activity of target enzymes, two advanced approaches including affinity screening and inhibition profiling showed great promises for a successful screening of bioactive compounds from natural sources. This review summarises the recent progress of separation-based methods for TYR inhibitors screening, with an emphasis on the principle, application, advantage, and drawback of each method along with perspectives in the future development of these screening techniques and screened hit compounds. |
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| Keywords: | Tyrosinase inhibitors natural products rapid screening separation methods |
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