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Extraordinary long detection window of a synthetic cannabinoid metabolite in human urine - Potential impact on therapeutic decisions

机译:人类尿液中合成大麻素代谢物的非凡的长检测窗口 - 潜在对治疗决策的影响

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Synthetic cannabinoids (SCs) have become established drugs of abuse. They play an increasing role in drug therapy, where abstinence control testing is required. Differentiation between recent drug uptake and uptake in the distant past is important for drug therapy. This study aimed to evaluate the detection window of a metabolite commonly used as a consumption marker for AB-FUBINACA and AMB-FUBINACA (synonym: FUB-AMB) in urine analysis. The acidic hydrolysis metabolite was quantified in urine samples of a drug user by applying a validated analytical method. The concentration profile of the metabolite was correlated with usage data of the subject. Pharmacokinetic properties of AB-FUBINACA were collected by analysis of serum and urine samples from a controlled administration study (single oral ingestion of AB-FUBINACA). Thirteen urine samples were taken without advance notice over 2 years. The metabolite was detected in the first urine sample at 0.77 ng/mg creatinine and subsequently in concentrations ranging from 0.06 to 0.29 ng/mg creatinine. Usage data showed credible abstinence from SCs during this period. The pharmacokinetic properties observed within the controlled self-administration study supported the hypothesis of distribution into deeper compartments and long-lasting elimination (serum concentration-time curve showing biphasic kinetics). An elimination phase of over 1 year after the last drug uptake seems plausible in cases of extensive consumption. To avoid misinterpretation of positive findings, we recommend testing patients with known SC use at the beginning of the abstinence program and to re-test continuously at short time intervals. These data enable the correct interpretation of analytical findings.
机译:合成大麻素(SCS)已成为已建立的滥用药物。它们在药物疗法中发挥着越来越大的作用,其中需要禁止控制测试。近距离过去的最近药物摄取和摄取之间的差异对于药物治疗是重要的。本研究旨在评估常用为AB-FUBACA和AMB-FUBINACA(同义词:FUB-AMB)的消费标志的代谢物的检测窗口。通过施加验证的分析方法,在药物使用者的尿液样本中定量酸性水解代谢物。代谢物的浓度谱与受试者的使用数据相关。通过来自受控管理研究的血清和尿液样本来收集AB-FUBINACA的药代动力学性质(唯一口服摄入AB-FUBACA)。在2年内没有提前通知,幼述了13个尿液样本。在0.77ng / mg肌酐的第一个尿液样品中检测到代谢物,随后以0.06至0.29ng / mg肌酐的浓度。在此期间,使用数据显示来自SCS的可信禁欲。在受控自我管理研究中观察到的药代动力学特性支持分布的假设进入更深的隔室和持久的消除(血清浓度 - 时间曲线,显示双相动力学)。在最后一次药物摄取后1岁以上的消除阶段在广泛消费的情况下似乎是合理的。为了避免误解积极调查结果,我们建议在禁忌方案开始时检测已知SC使用的患者,并在短时间内连续重新测试。这些数据能够正确地解释分析结果。

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