遗传毒性
乳蓟
传统医学
生物技术
生物
艾姆斯试验
菊科
毒理
细胞毒性
萃取(化学)
化学
诱变剂
生物测定
马兜铃
医学
药用植物
消费者安全
食品科学
毒性
化妆品
体外毒理学
作者
Peter David Ringel,Björn Feistel,Olaf Kelber,K Nieber
出处
期刊:Planta Medica
[Thieme Medical Publishers (Germany)]
日期:2026-01-14
卷期号:92 (06): 647-654
摘要
Abstract Herbal medicinal products (HMPs) prepared from the fruit of Silybum marianum are mainly used in the treatment of liver diseases and dyspeptic symptoms. Despite its long-standing use and good clinical safety profile, the safety assessment of such HMPs requires special attention to toxicological aspects that are difficult to detect clinically, especially genotoxic effects. The genotoxic potential of certain S. marianum extracts has been evaluated previously; however, some in vitro assays gave inconsistent results, which is why an EU list entry was not recommended by the Herbal Medicinal Product Committee (HMPC) of the European regulatory agency EMA. To provide a more comprehensive dataset for the evaluation of the genotoxic potential, six dry extracts covering the entire polarity range of extraction solvents were chosen in accordance with the “bracketing and matrixing” approach recommended by the HMPC. These extracts were subjected to the bacterial reverse mutation test, as specified in the OECD test guideline 471, which was performed both as a pre-incubation and plate incorporation assay. When testing up to 5 mg per plate or up to the solubility or cytotoxicity limits, none of the extracts showed signs of mutagenicity, suggesting that extracts of S. marianum fruit have no genotoxic potential. Within reasonable limits, these results may be extrapolated to other extracts based on the aforementioned “bracketing and matrixing” approach.
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