Lachenmeier Dirk W, Habel Stephanie, Fischer Berit, Herbi Frauke, Zerbe Yvonne, Bock Verena, Rajcic de Rezende Tabata, Walch Stephan G, Sproll Constanze
Chemisches und Veterinäruntersuchungsamt (CVUA) Karlsruhe, Karlsruhe, 76187, Germany.
F1000Res. 2019 Aug 8;8:1394. doi: 10.12688/f1000research.19931.7. eCollection 2019.
Cannabidiol (CBD)-containing products are widely marketed as over the counter products. Adverse effects reported in anecdotal consumer reports or during clinical studies were first assumed to be due to acid-catalysed cyclization of CBD to psychotropic Δ -tetrahydrocannabinol (Δ -THC) in the stomach after oral consumption. However, research of pure CBD solutions stored in simulated gastric juice or subjected to various storage conditions such as heat and light with specific liquid chromatographic/tandem mass spectrometric (LC/MS/MS) and ultra-high pressure liquid chromatographic/quadrupole time-of-flight mass spectrometric (UPLC-QTOF) analyses was unable to confirm THC formation. Another hypothesis for the adverse effects of CBD products may be residual Δ -THC concentrations in the products as contamination, because most of them are based on hemp extracts containing the full spectrum of cannabinoids besides CBD. Analyses of 413 hemp-based products of the German market (mostly CBD oils) confirmed this hypothesis: 48 products (12%) contained Δ -THC above the lowest observed adverse effect level (2.5 mg/day). Hence, it may be assumed that the adverse effects of some commercial CBD products are based on a low-dose effect of Δ -THC, with the safety of CBD itself currently being unclear with significant uncertainties regarding possible liver and reproductive toxicity. The safety, efficacy and purity of commercial CBD products is highly questionable, and all of the products in our sample collection showed various non-conformities to European food law such as unsafe Δ -THC levels, hemp extracts or CBD isolates as non-approved novel food ingredients, non-approved health claims, and deficits in mandatory food labelling requirements. In view of the growing market for such lifestyle products, the effectiveness of the instrument of food business operators' own responsibility for product safety and regulatory compliance must obviously be challenged, and a strong regulatory framework for hemp products needs to be devised.
含大麻二酚(CBD)的产品作为非处方产品被广泛销售。在消费者轶事报告或临床研究中报告的不良反应最初被认为是由于口服后CBD在胃中经酸催化环化形成精神活性的Δ-四氢大麻酚(Δ-THC)。然而,对储存在模拟胃液中或在热、光等各种储存条件下的纯CBD溶液进行特定液相色谱/串联质谱(LC/MS/MS)和超高压液相色谱/四极杆飞行时间质谱(UPLC-QTOF)分析,未能证实有THC形成。CBD产品产生不良反应的另一种假设可能是产品中存在作为污染物的残留Δ-THC浓度,因为大多数此类产品基于除CBD外还含有全谱大麻素的大麻提取物。对德国市场上413种基于大麻的产品(主要是CBD油)的分析证实了这一假设:48种产品(12%)所含的Δ-THC高于最低观察到的不良反应水平(2.5毫克/天)。因此,可以假定一些商业CBD产品的不良反应是基于Δ-THC的低剂量效应,而CBD本身的安全性目前尚不清楚,在可能的肝脏和生殖毒性方面存在重大不确定性。商业CBD产品的安全性、有效性和纯度非常值得怀疑,我们样本中的所有产品均显示出与欧洲食品法律存在各种不符之处,如不安全的Δ-THC水平、作为未经批准的新型食品成分的大麻提取物或CBD分离物、未经批准的健康声明以及强制性食品标签要求方面的缺陷。鉴于此类生活方式产品市场不断增长,食品企业经营者对产品安全和监管合规自行负责这一手段的有效性显然必须受到质疑,需要制定一个强有力的大麻产品监管框架。