Peschel Wieland
Centre for Pharmacognosy and Phytotherapy, Department for Pharmaceutical and Biological Chemistry, The School of Pharmacy, University College London, 29-39 Brunswick Square, London WC1N 1AX, UK.
Sci Pharm. 2016 Apr 18;84(3):567-584. doi: 10.3390/scipharm84030567.
Traditional tinctures of L. became obsolete before elucidation of the main cannabinoids and routine quality testing for medicines. In view of increasing medicinal use of cannabinoids and associated safety concerns, tinctures from a Δ9-tetrahydrocannabinol (THC)-type chemovar were studied. High-performance liquid chromatography with diode-array detection (HPLC/DAD) was used to determine THC, Δ9-tetrahydrocannabinolic acid A (THCA), cannabinol (CBN), cannabidiol (CBD), cannabidiolic acid (CBDA), cannabigerol (CBG), cannabigerolic acid (CBGA), cannflavin A/B, and total phenolics. Derived group and ratio markers describe absolute and relative profiles when varying plant part (flos, folium), extraction solvent (EtOH percentage), storage conditions ('shelf' or 'fridge' up to 15 months), and pasteurization (2 h 70 °C, 20 min 80 °C). Tinctures from female flowering tops contained ten-fold more cannabinoids than tinctures from leaves; tinctures (80%-90% EtOH) contained ten-fold more cannabinoids than tinctures (40% EtOH). The analysis of CBGA + CBG, the main co-cannabinoids aside from THCA + THC, appears more relevant than CBDA + CBD. The decarboxylation of THCA to THC-the main change during storage of freshly prepared tinctures-is after 15 months in the 'fridge' comparable to 3 months on the 'shelf'. Minimally increased CBN totals did not correlate to diminished totals of THCA and THC (up to 15% after 3 months 'shelf', 45% after 15 months 'fridge'). Instead, total cannabinoids or acidic/neutral cannabinoid ratios are better stability markers. Moderate changes after pasteurization and partial losses below 10% for total cannabinoids after 9 months 'fridge' indicate possibilities for a reasonable shelf life. Yet storage and use of non-stabilized tinctures remain critical without authorized specification and stability data because a consistent cannabinoid content is not guaranteed.
在主要大麻素被阐明以及药品常规质量检测之前,传统的L.酊剂就已过时。鉴于大麻素在医学上的使用日益增加以及相关的安全问题,对来自Δ9 - 四氢大麻酚(THC)型化学变种的酊剂进行了研究。采用带二极管阵列检测的高效液相色谱法(HPLC/DAD)来测定THC、Δ9 - 四氢大麻酚酸A(THCA)、大麻酚(CBN)、大麻二酚(CBD)、大麻二酚酸(CBDA)、大麻萜酚(CBG)、大麻萜酚酸(CBGA)、大麻黄素A/B和总酚类。当植物部位(花、叶)、提取溶剂(乙醇百分比)、储存条件(“货架”或“冰箱”,长达15个月)以及巴氏杀菌(70℃ 2小时,80℃ 20分钟)不同时,衍生基团和比率标记描述了绝对和相对特征。来自雌株花顶的酊剂所含大麻素比来自叶子的酊剂多十倍;(80% - 90%乙醇)酊剂所含大麻素比(40%乙醇)酊剂多十倍。对CBGA + CBG(除THCA + THC之外的主要共大麻素)的分析似乎比CBDA + CBD更具相关性。THCA脱羧转化为THC(新鲜制备酊剂储存期间的主要变化),在“冰箱”中存放15个月后与在“货架”上存放3个月相当。CBN总量略有增加与THCA和THC总量的减少无关(“货架”存放3个月后高达15%,“冰箱”存放15个月后为45%)。相反,总大麻素或酸性/中性大麻素比率是更好的稳定性标记。巴氏杀菌后有适度变化,“冰箱”存放9个月后总大麻素部分损失低于10%,这表明有合理保质期的可能性。然而,在没有授权规范和稳定性数据的情况下,未稳定化酊剂的储存和使用仍然至关重要,因为无法保证大麻素含量一致。