4.5 Review

Challenges in the quality of herbal medicinal products with a specific focus on contaminants

Journal

PHYTOCHEMICAL ANALYSIS
Volume 32, Issue 2, Pages 117-123

Publisher

WILEY
DOI: 10.1002/pca.2879

Keywords

contaminants; elemental impurities; herbal medicinal products; pesticide residue; pyrrolizidine alkaloids

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This review provides an overview of the legal requirements for testing potential contaminants in herbal drugs, including pesticide residues, heavy metals, microbiological purity, aflatoxins, and polycyclic aromatic hydrocarbons. It also discusses the decrease of pyrrolizidine alkaloids in herbal drugs over the past few years, while acknowledging that the issue cannot be completely solved in the near future.
Background The complex regulatory framework for the quality of herbal medicinal products, in particular with regard to potential contaminants, consists of legal provisions including Pharmacopoeia requirements, relating to limits as well as in most cases to methods for determination. Objective This review intends to provide an overview on the legal requirements for testing potential contaminants in herbal drugs used for the production of herbal medicinal products. Methodology The following issues are described and discussed: For the assessment of pesticide residues, Chapter 2.8.13 of the European Pharmacopoeia and Regulation (EC) 396/2005 applies, for heavy metals the general Pharmacopoeia monograph as well as the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Q3D guideline on elemental impurities. The Pharmacopoeia also includes limits and acceptance criteria for microbiological purity and aflatoxins, respectively. Polycyclic aromatic hydrocarbons are mentioned in Regulation (EC) 1881/2006 for food as well as in a Reflection Paper on herbal medicinal products. For several years, a potential contamination with pyrrolizidine alkaloids was discussed which led to measures being imposed on industry and health authorities. Results Various examples demonstrate that the evaluation of data from daily analytical practice is extremely useful to gain an overview on the occurrence of residues and/or contaminants in herbal drugs and herbal preparations. Such evaluations might assist manufacturers in their individual risk assessment and the definition of their testing strategies and contribute to guarantee the quality and safety of the marketed products. Conclusion Annual data evaluations demonstrate that a remarkable decrease of the pyrrolizidine alkaloid content burden in herbal drugs and extracts used for the production of herbal medicinal products has been achieved over the past few years. However, it has also become clear that this issue cannot be completely solved in the near future.

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