Krill Christian, Rochfort Simone, Spangenberg German
Agriculture Victoria, AgriBio, Centre for AgriBioscience, Bundoora, VIC 3083, Australia.
Metabolites. 2020 Jul 6;10(7):276. doi: 10.3390/metabo10070276.
Cannabis and its secondary metabolite content have recently seen a surge in research interest. Cannabis terpenes and terpenoids in particular are increasingly the focus of research efforts due to the possibility of their contribution to the overall therapeutic effect of medicinal cannabis. Current methodology to quantify terpenes in cannabis biomass mostly relies on large quantities of biomass, long extraction protocols, and long GC gradient times, often exceeding 60 min. They are therefore not easily applicable in the high-throughput environment of a cannabis breeding program. The method presented here, however, is based on a simple hexane extract from 40 mg of biomass, with 50 μg/mL dodecane as internal standard, and a gradient of less than 30 min. The method can detect 48 individual terpenes and terpenoids and was validated for selectivity, linearity, LOD/LOQ, precision, intermediate precision, and accuracy (recovery) for 22 terpenes and terpenoids. The validation parameters are comparable to previously published studies that employ significantly longer runtimes and/or more complex extraction protocols. It is currently being applied to medicinal cannabis precision breeding programs.
大麻及其次生代谢物含量最近在研究兴趣方面激增。尤其是大麻萜类化合物,由于它们可能对药用大麻的整体治疗效果有贡献,越来越成为研究工作的重点。目前用于量化大麻生物量中萜类化合物的方法大多依赖大量生物量、冗长的提取方案和长达60分钟以上的长气相色谱梯度时间。因此,它们不容易应用于大麻育种计划的高通量环境。然而,这里介绍的方法基于从40毫克生物量中简单的己烷提取物,以50微克/毫升十二烷作为内标,梯度时间少于30分钟。该方法可以检测48种单个萜类化合物和类萜化合物,并针对22种萜类化合物和类萜化合物的选择性、线性、检测限/定量限、精密度、中间精密度和准确度(回收率)进行了验证。这些验证参数与之前发表的研究相当,而之前的研究采用了长得多的运行时间和/或更复杂的提取方案。该方法目前正在应用于药用大麻精准育种计划。