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Predicting the Potential for Cannabinoids to Precipitate Pharmacokinetic Drug Interactions via Reversible Inhibition or Inactivation of Major Cytochromes P450.预测大麻素通过可逆抑制或失活主要细胞色素 P450 而引发药物代谢动力学药物相互作用的潜力。
Drug Metab Dispos. 2020 Oct;48(10):1008-1017. doi: 10.1124/dmd.120.000073. Epub 2020 Jun 25.
2
Clinical Data for the Use of Cannabis-Based Treatments: A Comprehensive Review of the Literature.临床使用大麻类药物治疗的数据:文献综述
Ann Pharmacother. 2020 Nov;54(11):1109-1143. doi: 10.1177/1060028020930189. Epub 2020 Jun 2.
3
Reduced urinary opioid levels from pain management patients associated with marijuana use.疼痛管理患者中与使用大麻相关的尿类阿片水平降低。
Pain Manag. 2019 Sep;9(5):441-447. doi: 10.2217/pmt-2019-0017. Epub 2019 Sep 9.
4
Cannabis Use Motivations among Adults Prescribed Opioids for Pain versus Opioid Addiction.开具阿片类药物用于止痛的成年人与阿片类药物成瘾者使用大麻的动机
Pain Manag Nurs. 2020 Feb;21(1):43-47. doi: 10.1016/j.pmn.2019.06.009. Epub 2019 Jul 30.
5
Medical Cannabis: Effects on Opioid and Benzodiazepine Requirements for Pain Control.医用大麻:对阿片类药物和苯二氮䓬类药物控制疼痛需求的影响。
Ann Pharmacother. 2019 Nov;53(11):1081-1086. doi: 10.1177/1060028019854221. Epub 2019 May 25.
6
Medicinal use of cannabis based products and cannabinoids.大麻制品和大麻素的药用
BMJ. 2019 Apr 4;365:l1141. doi: 10.1136/bmj.l1141.
7
Engagement in online pain self-management improves pain in adults on medication-assisted behavioral treatment for opioid use disorders.参与在线疼痛自我管理可改善接受阿片类药物使用障碍药物辅助行为治疗的成年人的疼痛。
Addict Behav. 2018 Nov;86:130-137. doi: 10.1016/j.addbeh.2018.04.019. Epub 2018 Apr 27.
8
Pharmacokinetic and behavioural profile of THC, CBD, and THC+CBD combination after pulmonary, oral, and subcutaneous administration in rats and confirmation of conversion in vivo of CBD to THC.在大鼠中经肺部、口服和皮下给予 THC、CBD 和 THC+CBD 组合后的药代动力学和行为特征,以及 CBD 体内向 THC 转化的确认。
Eur Neuropsychopharmacol. 2017 Dec;27(12):1223-1237. doi: 10.1016/j.euroneuro.2017.10.037. Epub 2017 Nov 10.
9
A Cross-Sectional Survey of Medical Cannabis Users: Patterns of Use and Perceived Efficacy.医用大麻使用者的横断面调查:使用模式与感知疗效
Cannabis Cannabinoid Res. 2016 Jun 1;1(1):131-138. doi: 10.1089/can.2016.0007. eCollection 2016.
10
Human Metabolites of Cannabidiol: A Review on Their Formation, Biological Activity, and Relevance in Therapy.大麻二酚的人体代谢产物:关于其形成、生物活性及治疗相关性的综述
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口服氢可酮-对乙酰氨基酚与吸入大麻烟雾之间的药物相互作用:一例报告

Drug-Drug Interaction Between Orally Administered Hydrocodone-Acetaminophen and Inhalation of Cannabis Smoke: A Case Report.

作者信息

Bindler Ross Jason, Watson Christy J W, Lyons Abram J, Skeiky Lillian, Lewis Jamie, McDonell Michael, Lazarus Philip, Wilson Marian

机构信息

Washington State University, Spokane, WA, USA.

Northwest Spine and Pain Medicine, Spokane, WA, USA.

出版信息

Hosp Pharm. 2022 Aug;57(4):518-525. doi: 10.1177/00185787211061374. Epub 2021 Dec 7.

DOI:10.1177/00185787211061374
PMID:35898257
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9310317/
Abstract

OBJECTIVE

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.

CASE SUMMARY

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.

RESULTS

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.

DISCUSSION

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.

CONCLUSION AND RELEVANCE

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.

摘要

目的

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。

病例摘要

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。

结果

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。

讨论

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。

结论与意义

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。