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大麻素更精简且更环保的分析

Leaner and greener analysis of cannabinoids.

作者信息

Mudge Elizabeth M, Murch Susan J, Brown Paula N

机构信息

Natural Health & Food Products Research, British Columbia Institute of Technology, 3700 Willingdon Ave, Burnaby, British Columbia, V5G 3H2, Canada.

Department of Chemistry, University of British Columbia, 3247 University Way, Kelowna, British Columbia, V1V 1V7, Canada.

出版信息

Anal Bioanal Chem. 2017 May;409(12):3153-3163. doi: 10.1007/s00216-017-0256-3. Epub 2017 Feb 23.

DOI:10.1007/s00216-017-0256-3
PMID:28233028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5395585/
Abstract

There is an explosion in the number of labs analyzing cannabinoids in marijuana (Cannabis sativa L., Cannabaceae) but existing methods are inefficient, require expert analysts, and use large volumes of potentially environmentally damaging solvents. The objective of this work was to develop and validate an accurate method for analyzing cannabinoids in cannabis raw materials and finished products that is more efficient and uses fewer toxic solvents. An HPLC-DAD method was developed for eight cannabinoids in cannabis flowers and oils using a statistically guided optimization plan based on the principles of green chemistry. A single-laboratory validation determined the linearity, selectivity, accuracy, repeatability, intermediate precision, limit of detection, and limit of quantitation of the method. Amounts of individual cannabinoids above the limit of quantitation in the flowers ranged from 0.02 to 14.9% w/w, with repeatability ranging from 0.78 to 10.08% relative standard deviation. The intermediate precision determined using HorRat ratios ranged from 0.3 to 2.0. The LOQs for individual cannabinoids in flowers ranged from 0.02 to 0.17% w/w. This is a significant improvement over previous methods and is suitable for a wide range of applications including regulatory compliance, clinical studies, direct patient medical services, and commercial suppliers.

摘要

分析大麻(大麻科大麻属植物大麻)中大麻素的实验室数量呈爆炸式增长,但现有方法效率低下,需要专业分析人员,且使用大量可能对环境造成破坏的溶剂。这项工作的目的是开发并验证一种准确的方法,用于分析大麻原材料和成品中的大麻素,该方法更高效且使用更少的有毒溶剂。基于绿色化学原理,采用统计指导的优化方案,开发了一种用于分析大麻花和油中八种大麻素的高效液相色谱 - 二极管阵列检测(HPLC - DAD)方法。单实验室验证确定了该方法的线性、选择性、准确性、重复性、中间精密度、检测限和定量限。花中各单一大麻素的定量限以上含量范围为0.02至14.9%(w/w),重复性的相对标准偏差范围为0.78至10.08%。使用HorRat比率确定的中间精密度范围为0.3至2.0。花中各单一大麻素的定量限范围为0.02至0.17%(w/w)。这比以前的方法有显著改进,适用于广泛的应用,包括法规遵从性、临床研究、直接患者医疗服务和商业供应商。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64fc/5395585/d0ea3aec2e79/216_2017_256_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64fc/5395585/d0ea3aec2e79/216_2017_256_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64fc/5395585/d0ea3aec2e79/216_2017_256_Fig3_HTML.jpg

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