Pharmaceutical quality of herbal medicinal products and dietary supplements – a case study with oral solid formulations containing Lavandula species

IF 4.7 3区 医学 Q1 PHARMACOLOGY & PHARMACY European Journal of Pharmaceutical Sciences Pub Date : 2025-05-01 Epub Date: 2025-02-12 DOI:10.1016/j.ejps.2025.107042
Banaz Jalil , Michael Heinrich
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Abstract

The effectiveness and safety of regulated herbal medicinal products and dietary/food supplements are key areas of research. However, limited evidence exists of their pharmaceutical performance quality (including the standard in the respective pharmacopeial monographs). We evaluated the applicability of the European Pharmacopoeia general chapter protocols for disintegration testing of oral dosage forms using 73 products containing Lavandula species. Several Lavandula species, hybrids and cultivars are important medicinal plants globally in the phytopharmaceuticals and dietary/food supplement industry, including Lavandula Mill., traditionally used to treat conditions linked to nervousness and sleep disorders. We evaluate the pharmaceutical performance quality, particularly the in vitro disintegration and the phytochemical quality of 73 Lavandula oral dosage forms of single and multi–ingredients with different regulatory statuses. The phytochemical quality testing showed that 63 % of products contain less or none of the main marker compounds (e.g., linalool, linalyl acetate, and cineole). There was also considerable variability of the main marker compounds between products, with some containing ‘often/sometimes undeclared’ and significant amounts of rapeseed and sunflower oils as excipients. The pharmaceutical performance quality testing showed that 30 % of oral solid formulations always failed the disintegration testing (seven soft gels, ten hard shells, and five tablets/caplets). Pass rates for gelatine-based capsules were higher than for non-gelatine (cellulose-based) capsules. Overall, our findings highlighted problems with the pharmaceutical performance and phytochemical quality of the investigated products. These results have implications for the interpretations of the benefits and risks of phytopharmaceuticals used as compared to dietary/food supplements.

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草药产品和膳食补充剂的药品质量——含薰衣草属植物的口服固体制剂的案例研究。
受监管的草药产品和膳食/食品补充剂的有效性和安全性是研究的关键领域。然而,它们的药物性能质量(包括各自药典各论中的标准)的证据有限。我们评估了欧洲药典通章规程对含有薰衣草属73种产品的口服剂型崩解试验的适用性。在植物制药和膳食/食品补充剂行业中,一些薰衣草物种、杂交品种和栽培品种是全球重要的药用植物,其中包括L. angustifolia Mill。传统上用于治疗与神经紧张和睡眠障碍有关的疾病。对73种不同监管状态的单成分和多成分薰衣草口服剂型的药物性能质量,特别是体外崩解和植物化学质量进行了评价。植物化学质量检测表明,63%的产品含有较少或不含主要标记化合物(如芳樟醇、醋酸芳樟醇和桉树脑)。产品之间的主要标记化合物也存在相当大的差异,有些产品含有“经常/有时未申报”和大量的菜籽油和葵花籽油作为辅料。药品性能质量检测结果显示,30%的口服固体制剂崩解不合格(7个软凝胶、10个硬壳、5个片/片)。明胶基胶囊的通过率高于非明胶(纤维素基)胶囊。总的来说,我们的研究结果突出了所研究产品的药物性能和植物化学质量问题。这些结果对解释与膳食/食品补充剂相比使用植物药的益处和风险具有启示意义。
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来源期刊
CiteScore
9.60
自引率
2.20%
发文量
248
审稿时长
50 days
期刊介绍: The journal publishes research articles, review articles and scientific commentaries on all aspects of the pharmaceutical sciences with emphasis on conceptual novelty and scientific quality. The Editors welcome articles in this multidisciplinary field, with a focus on topics relevant for drug discovery and development. More specifically, the Journal publishes reports on medicinal chemistry, pharmacology, drug absorption and metabolism, pharmacokinetics and pharmacodynamics, pharmaceutical and biomedical analysis, drug delivery (including gene delivery), drug targeting, pharmaceutical technology, pharmaceutical biotechnology and clinical drug evaluation. The journal will typically not give priority to manuscripts focusing primarily on organic synthesis, natural products, adaptation of analytical approaches, or discussions pertaining to drug policy making. Scientific commentaries and review articles are generally by invitation only or by consent of the Editors. Proceedings of scientific meetings may be published as special issues or supplements to the Journal.
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