Division on Substance Abuse, New York State Psychiatric Institute and Department of Psychiatry, Columbia University Medical Center, USA.
Department of Pharmacology and Toxicology, Virginia Commonwealth University, USA.
Neuropharmacology. 2018 May 15;134(Pt A):92-100. doi: 10.1016/j.neuropharm.2017.11.020. Epub 2017 Nov 14.
Synthetic cannabinoids (SCs) are a significant public health concern given their widespread use and severe effects associated with intoxication. However, there is a paucity of controlled human studies investigating the behavioral and physiological effects and pharmacokinetics of these compounds. Designing a reliable method to administer consistent, concentration-dependent synthetic cannabinoids is an integral component of controlled study of these compounds. Further, optimizing methods to assess the parent compounds and metabolites in plasma is critical in order to be able to establish their pharmacokinetics after administration. To develop a reliable method to administer smokable, concentration-dependent SCs, cigarettes were prepared with plant matter adulterated with increasing concentrations of the first generation cannabinoids found in SC products, JWH-018 and JWH-073. Cigarettes were assessed 1-6 months after preparation using ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) to determine compound stability over time and concentration consistency throughout the cigarettes. Optimal conditions to detect metabolites in human plasma as a function of storage temperature (-4 °C to -80 °C) and time (24 h - 1 month) were also determined. Analyses verified that the method utilized to develop SC cigarettes yielded consistent, concentration-dependent products within 25% of the expected concentrations. JWH-018, JWH-073 and metabolites in spiked plasma were stable under the time and temperature conditions; concentrations were within ±20% of target values. These studies provide techniques and methods to conduct controlled investigations of the dose-dependent effects of first generation SCs to begin understanding risks associated with use. This article is part of the Special Issue entitled 'Designer Drugs and Legal Highs.'
合成大麻素 (SCs) 是一个严重的公共卫生问题,因为它们被广泛使用,并与中毒相关的严重影响。然而,目前还缺乏关于这些化合物的行为和生理效应及药代动力学的对照人体研究。设计一种可靠的方法来施用一致、浓度依赖性的合成大麻素是这些化合物对照研究的一个重要组成部分。此外,优化评估母体化合物和代谢物在血浆中的方法对于建立其给药后的药代动力学是至关重要的。为了开发一种可靠的方法来施用可吸食、浓度依赖性的 SCs,用植物物质掺杂第一代大麻素制备香烟,这些第一代大麻素是在 SC 产品中发现的 JWH-018 和 JWH-073。在制备后 1-6 个月使用超高效液相色谱-串联质谱 (UPLC-MS/MS) 评估香烟,以确定化合物随时间的稳定性和香烟中整个浓度的一致性。还确定了检测人类血浆中代谢物的最佳条件,包括储存温度 (-4°C 至-80°C) 和时间 (24 小时至 1 个月)。分析证实,用于开发 SC 香烟的方法产生了一致、浓度依赖性的产品,与预期浓度的偏差在 25%以内。JWH-018、JWH-073 和加标血浆中的代谢物在时间和温度条件下稳定;浓度在目标值的±20%以内。这些研究提供了技术和方法,用于进行第一代 SC 剂量依赖性效应的对照研究,以开始了解与使用相关的风险。本文是特刊“设计药物和合法兴奋剂”的一部分。