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开发用于大麻素定量的稳健标准化分析程序:为新兴的大麻基制药行业奠定基础。

Developing Robust Standardised Analytical Procedures for Cannabinoid Quantification: Laying the Foundations for an Emerging Cannabis-Based Pharmaceutical Industry.

作者信息

Welling Matthew T, Liu Lei, Hazekamp Arno, Dowell Ashley, King Graham J

机构信息

Southern Cross Plant Science, Southern Cross University, Lismore, New South Wales, Australia.

Hazekamp Herbal Consulting BV, Leiden, The Netherlands.

出版信息

Med Cannabis Cannabinoids. 2019 Feb 25;2(1):1-13. doi: 10.1159/000496868. eCollection 2019 Sep.

Abstract

The plant genus is a prolific producer of unique pharmaceutically relevant metabolites, commonly referred to as cannabinoids. Robust and standardised methods for the quantification of cannabinoids within botanical and drug forms is a critical step forward for an emerging -based pharmaceutical industry, which is poised for rapid expansion. Despite a growing body of analytical methods for the quantification of cannabinoids, few have been validated using internationally accredited guidelines. Moreover, standardised methods have yet to be developed for application at various stages of manufacture as well as for different levels of processing and refinement. Validation parameters for establishing robust standardised methods for cannabinoid quantification within -based drug forms are critically discussed. Determining an appropriate level of specificity (discrimination) among heterogeneous botanical matrices as well as evaluating accuracy (recovery) and inter-laboratory precision (reproducibility) within strict and volatile regulatory environments are potential obstacles to the establishment of robust analytical procedures. We argue that while some of these challenges remain unique to , others are common to botanical-based drug development and manufacture. In order to address potential barriers to analytical method standardisation, a collaborative research initiative inclusive of academic and commercial stakeholders is proposed.

摘要

该植物属是独特的具有药学相关性的代谢产物(通常称为大麻素)的多产生产者。对于新兴的基于植物的制药行业而言,建立强大且标准化的方法来定量植物和药物形式中的大麻素是向前迈出的关键一步,该行业正准备迅速扩张。尽管用于定量大麻素的分析方法越来越多,但很少有方法按照国际认可的指南进行验证。此外,尚未开发出适用于制造各个阶段以及不同加工和精制水平的标准化方法。本文对建立强大的标准化方法以定量基于植物的药物形式中的大麻素的验证参数进行了批判性讨论。在异质植物基质中确定适当的特异性(区分度)水平,以及在严格且多变的监管环境中评估准确性(回收率)和实验室间精密度(再现性),是建立强大分析程序的潜在障碍。我们认为,虽然其中一些挑战对于该植物属来说仍然是独特的,但其他一些挑战是基于植物的药物开发和制造所共有的。为了解决分析方法标准化的潜在障碍,我们提出了一项由学术和商业利益相关者共同参与的研究倡议。

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