Bettiol Alessandra, Lombardi Niccolò, Crescioli Giada, Maggini Valentina, Gallo Eugenia, Mugelli Alessandro, Firenzuoli Fabio, Baronti Roberto, Vannacci Alfredo
Section of Pharmacology and Toxicology, Department of Neurosciences, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy.
Tuscan Regional Centre of Pharmacovigilance and Phytovigilance, Florence, Italy.
Front Pharmacol. 2019 Jan 17;9:1543. doi: 10.3389/fphar.2018.01543. eCollection 2018.
Magistral preparations of therapeutic cannabis are extracted from standardized products imported from Holland or from the Florence Military Pharmaceutical Chemical Works, but extraction protocols differ among galenic laboratories. This study assessed the inter-laboratory variability in concentrations of cannabidiol (CBD), cannabinol (CBN), tetrahydrocannabinol (THC), and tetrahydrocannabinolic acid (THCA) among different magistral oil preparations. 219 samples of Bediol, Bedrobinol, Bedrolite or FM-2 70 or 100 mg/ml in oil were collected from 3 laboratories. Concentrations of CBD, CBN, THC, and THCA were quantified by high-pressure liquid chromatography; inter-laboratories variability was assessed using the Kruskal-Wallis test. A significant variability in CBD and THC concentrations was found for Bediol 70 mg/ml samples from 2 laboratories [for CBD: median 5.4 (range 4.8-6.6) vs. 6.1 (4.9-7.2) mg/ml, = 0.033; for THC: 3.6 (3.1-3.9) vs. 4.0 (2.6-5.1) mg/ml, = 0.020]. As for Bediol 100 mg/ml, a significant variability emerged in THC concentrations among the three considered laboratories [5.7 (-) vs. 4.2 (1.5-4.8) vs. 5.2 (4.2-6.9), = 0.030]. No significant inter-laboratory variability emerged for Bedrocan and Bedrolite. Concentrations of CBD, CBN, and THC were <LOQ in all Bedrocan samples, and CBN and THCA were <LOQ in all Bedrolite samples. As for FM-2, a significant inter-laboratories variability was found for CBD concentrations. Quantitative variability of cannabinoids in magistral preparations might impact on the efficacy and safety of therapeutic cannabis. A standardized protocol is needed to guarantee a homogeneous product and patients' therapeutic continuity.
药用大麻的调配制剂是从荷兰进口的标准化产品或佛罗伦萨军事制药化工厂提取的,但不同盖伦制剂实验室的提取方案有所不同。本研究评估了不同药用油制剂中大麻二酚(CBD)、大麻酚(CBN)、四氢大麻酚(THC)和四氢大麻酸(THCA)浓度的实验室间变异性。从3个实验室收集了219份浓度为70或100mg/ml的Bediol、Bedrobinol、Bedrolite或FM-2油样。通过高压液相色谱法定量测定CBD、CBN、THC和THCA的浓度;使用Kruskal-Wallis检验评估实验室间的变异性。在来自2个实验室的70mg/ml Bediol样品中,发现CBD和THC浓度存在显著变异性[CBD:中位数5.4(范围4.8-6.6)对6.1(4.9-7.2)mg/ml,P=0.033;THC:3.6(3.1-3.9)对4.0(2.6-5.1)mg/ml,P=0.020]。对于100mg/ml的Bediol,在三个考虑的实验室中,THC浓度出现了显著变异性[5.7(-)对4.2(1.5-4.8)对5.2(4.2-6.9),P=0.