Hayley Amie C, Downey Luke A, Hansen Glyn, Dowell Ashley, Savins Dale, Buchta Richard, Catubig Reinilda, Houlden Robert, Stough Con K K
Centre for Human Psychopharmacology, Swinburne University of Technology, Hawthorn, Australia.
Centre for Human Psychopharmacology, Swinburne University of Technology, Hawthorn, Australia; Institute for Breathing and Sleep, Austin Hospital, Melbourne, Australia.
Forensic Sci Int. 2018 Mar;284:101-106. doi: 10.1016/j.forsciint.2017.12.033. Epub 2017 Dec 24.
Hemp-derivative (Cannabis sativa L.) food products containing trace levels of Δ-9-tetrahydrocannabinol (THC) are proposed for consumption in Australia and New Zealand; however, it is unclear whether use of these products will negatively affect existing drug screening protocols. This double-blind, within-subjects, cross-over trial assessed 35 adults (17 male; 18 female), aged 22-52 years [Mean=30.7, Standard Deviation (S.D)±7.6]. Low dose THC oil [5mL bearer sesame oil containing 10mg/kg THC (0.046mg THC per 5mL dose)]; high dose THC oil [5mL bearer sesame oil containing 20mg/kg THC (0.092mg THC per 5mL dose)]; and a placebo oil (THC negative) was consumed during a three-week protocol. The Securetec Drugwipe II Twin device assessed THC presence (cut-off 20ng/mL) in oral fluid at baseline, at 5, 30, 60, 120 and 240min post-treatment. Blood was drawn at baseline, 30, 120 and 240min post-treatment, and urine at baseline and 240min post-treatment. No THC was detected in oral fluid, blood or urine samples at any time-point following consumption of the low or high THC dose. Trace concentrations of 11-nor-Δ9-tetrahydrocannabinol-9-carboxylic acid (THCa) were detected in blood 4-h after consumption of the high THC treatment (M=0.0001mg/L) and in urine at 4-h post consumption of both low and high THC treatments (M=0.0001mg/L and 0.0004mg/L, respectively). Consumption of low-content THC oil does not result in positive biological assessments. It is therefore highly unlikely that ingestion of products containing these levels of THC will negatively impact existing region-specific drug driving enforcement protocols.
在澳大利亚和新西兰,含有微量Δ-9-四氢大麻酚(THC)的大麻衍生物(大麻)食品被提议用于消费;然而,尚不清楚使用这些产品是否会对现有的药物筛查方案产生负面影响。这项双盲、受试者内、交叉试验评估了35名成年人(17名男性;18名女性),年龄在22至52岁之间[平均=30.7,标准差(S.D)±7.6]。在为期三周的方案中,受试者食用了低剂量THC油[5mL载体芝麻油,含10mg/kg THC(每5mL剂量含0.046mg THC)];高剂量THC油[5mL载体芝麻油,含20mg/kg THC(每5mL剂量含0.092mg THC)];以及一种安慰剂油(THC阴性)。使用Securetec Drugwipe II Twin设备在基线时以及治疗后5、30、60、120和240分钟评估口腔液中THC的存在情况(截断值为20ng/mL)。在基线时、治疗后30、120和240分钟采集血液,在基线时和治疗后240分钟采集尿液。在食用低剂量或高剂量THC后,任何时间点的口腔液、血液或尿液样本中均未检测到THC。在食用高剂量THC治疗4小时后,血液中检测到微量浓度的11-去甲-Δ9-四氢大麻酚-9-羧酸(THCa)(M=0.0001mg/L),在食用低剂量和高剂量THC治疗后4小时的尿液中也检测到THCa(分别为M=0.0001mg/L和0.0004mg/L)。食用低含量THC油不会导致阳性生物学评估结果。因此,摄入含有这些THC水平的产品极不可能对现有的特定地区药物驾驶执法方案产生负面影响。