Bindler Ross Jason, Watson Christy J W, Lyons Abram J, Skeiky Lillian, Lewis Jamie, McDonell Michael, Lazarus Philip, Wilson Marian
Washington State University, Spokane, WA, USA.
Northwest Spine and Pain Medicine, Spokane, WA, USA.
Hosp Pharm. 2022 Aug;57(4):518-525. doi: 10.1177/00185787211061374. Epub 2021 Dec 7.
To determine if a 2-day protocol measuring pharmacokinetic and pharmacodynamic characteristics can demonstrate drug-drug interactions when smoked cannabis is added to orally administered hydrocodone/acetaminophen combination products.
A 51-year-old non-Hispanic white male with chronic pain diagnoses participated in a 2-day pilot protocol. The participant attended two 7-hour in-lab days where he received 10 blood draws each day and completed self-administered pain and anxiety surveys. For both days, the participant took his prescribed dose of hydrocodone/acetaminophen (1/2 tablet of 7.5 mg/325 mg combination product) with the addition of 1 smoked pre-rolled marijuana cigarette (labeled as 0.5 g; 22.17% Δ9-tetrahydrocannabinol; 0.12% cannabidiol) on Day 2. Blood specimens were analyzed using mass spectrometry to quantify the difference of plasma hydrocodone levels between Day 1 and Day 2.
Compared to Day 1, lower levels of pain and anxiety were reported during Day 2 with the addition of cannabis to oral hydrocodone/acetaminophen. Day 2 pharmacokinetic analysis also revealed more rapid absorption and overall lower levels of hydrocodone in plasma.
Lower hydrocodone plasma levels in Day 2 may indicate cannabis's effect on metabolism and reduce the risk of opioid toxicity. The quicker absorption rate of hydrocodone could explain lower pain and anxiety scores reported on the second day.
A 2-day protocol was able to capture differences across time in pharmacokinetic and pharmacodynamic measurements. Larger studies can be designed to better characterize the potential drug-drug interaction of cannabis and opioids.
确定一个为期2天的测量药代动力学和药效学特征的方案,在口服氢可酮/对乙酰氨基酚复方制剂中添加吸食大麻时,是否能证明药物相互作用。
一名患有慢性疼痛诊断的51岁非西班牙裔白人男性参与了一项为期2天的试点方案。该参与者参加了两个7小时的实验室日,每天接受10次采血,并完成自我管理的疼痛和焦虑调查。两天内,该参与者均服用规定剂量的氢可酮/对乙酰氨基酚(1片7.5毫克/325毫克复方制剂的半片),第二天还添加了1支预卷好的吸食大麻香烟(标签显示为0.5克;22.17%的Δ9-四氢大麻酚;0.12%的大麻二酚)。使用质谱分析法对血样进行分析,以量化第1天和第2天血浆中氢可酮水平的差异。
与第1天相比,第2天在口服氢可酮/对乙酰氨基酚中添加大麻后,报告的疼痛和焦虑水平较低。第2天的药代动力学分析还显示,氢可酮的吸收更快,血浆中的总体水平更低。
第2天氢可酮血浆水平较低可能表明大麻对代谢有影响,并降低了阿片类药物毒性风险。氢可酮更快的吸收率可以解释第二天报告的较低疼痛和焦虑评分。
一个为期2天的方案能够捕捉药代动力学和药效学测量随时间的差异。可以设计更大规模的研究,以更好地描述大麻与阿片类药物之间潜在的药物相互作用。