捷克市场中草药产品中赭曲霉毒素A和桔霉素含量调查。

IF 4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Jakub Toman, Darina Pickova, Karolina Brandova, Vladimir Ostry, Frantisek Malir
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引用次数: 0

摘要

药用植物被广泛用作膳食补充剂,以鼓励疾病预防和支持治疗各种健康失调。不幸的是,有几种植物被霉菌毒素污染,这可能会压倒植物可能具有的任何有益作用。目的:测定中药产品中赭曲霉毒素A (OTA)和柑橘霉素(CIT)的含量。方法:2020-2021年在捷克市场购买不同MHP类型的样品60份。采用高效液相色谱法测定两种真菌毒素,荧光检测器采用免疫亲和柱作为前处理。结果:有40%和27%的样品超过定量限,其中OTA和CIT的浓度分别高达826.62 ng/g和472.79 ng/g。在6种MHP型中证实了共发性。结论:MHP可能是OTA和CIT的重要来源,为了保护MHP使用者的健康,有必要继续监测MHP中真菌毒素的存在。在这项研究中,新的草药OTA法规在欧盟生效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of Ochratoxin A and Citrinin Occurrence in Medicinal Herbal Products from the Czech Market.

Introduction: Medicinal plants are extensively utilized as dietary supplements to encourage disease prevention and to support the treatment of various health disorders. Unfortunately, several plants are known for mycotoxin contamination, which may overwhelm any beneficial effects the plants might have.

Objective: The purpose of the study was to determine the presence of ochratoxin A (OTA) and citrinin (CIT) in medicinal herbal products (MHP).

Methods: Sixty samples of different MHP types were purchased on the Czech market during 2020-2021. Both mycotoxins were determined using high-performance liquid chromatography with a fluorescence detector with immunoaffinity columns employed as a pretreatment.

Results: In total, 40% and 27% of samples were above the limit of quantification with the concentrations ranging up to 826.62 ng/g and 472.79 ng/g for OTA and CIT, respectively. The co-occurrence was confirmed in six MHP types.

Conclusions: MHP could be a significant source of OTA and CIT. To protect the health of MHP users, it is desirable to continue monitoring the presence of mycotoxins in MHP. During this study, new OTA regulations for herbs came into force in the EU.

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来源期刊
Drug Safety
Drug Safety 医学-毒理学
CiteScore
7.60
自引率
7.10%
发文量
112
审稿时长
6-12 weeks
期刊介绍: Drug Safety is the official journal of the International Society of Pharmacovigilance. The journal includes: Overviews of contentious or emerging issues. Comprehensive narrative reviews that provide an authoritative source of information on epidemiology, clinical features, prevention and management of adverse effects of individual drugs and drug classes. In-depth benefit-risk assessment of adverse effect and efficacy data for a drug in a defined therapeutic area. Systematic reviews (with or without meta-analyses) that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. Original research articles reporting the results of well-designed studies in disciplines such as pharmacoepidemiology, pharmacovigilance, pharmacology and toxicology, and pharmacogenomics. Editorials and commentaries on topical issues. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Drug Safety Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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