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Stability studies of amphetamine and ephedrine derivatives in urine

机译:苯丙胺和麻黄碱衍生物在尿液中的稳定性研究

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Knowledge of the stability of drugs in biological specimens is a critical consideration for the interpretation of analytical results. Identification of proper storage conditions has been a matter of concern for most toxicology laboratories (both clinical and forensic), and the stability of drugs of abuse has been extensively studied. This concern should be extended to other areas of analytical chemistry like antidoping control. In this work, the stability of ephedrine derivatives (ephedrine, norephedrine, methylephedrine, pseudoephedrine, and norpseudoephedrine), and amphetamine derivatives (amphetamine, methamphetamine, 3,4-methylenedioxyamphetamine (MDA), and 3,4-methylenedioxymethamphetamine (MDMA)) in urine has been studied. Spiked urine samples were prepared for stability testing. Urine samples were quantified by GC/NPD or GC/MS. The homogeneity of each batch of sample was verified before starting the stability study. The stability of analytes was evaluated in sterilized and non-sterilized urine samples at different storage conditions. For long-term stability testing, analyte concentration in urine stored at 4 degrees C and -20 degrees C was determined at different time intervals for 24 months for sterile urine samples, and for 6 months for non-sterile samples. For short-term stability testing, analyte concentration was evaluated in liquid urine stored at 37 degrees C for 7 days. The effect of repeated freezing (at -20 degrees C) and thawing (at room temperature) was also studied in sterile urine for up to three cycles. No significant loss of the analytes under study was observed at any of the investigated conditions. These results show the feasibility of preparing reference materials containing ephedrine and amphetamine derivatives to be used for quality control purposes. (c) 2006 Elsevier B.V. All rights reserved.
机译:了解生物样品中药物的稳定性是解释分析结果的关键考虑因素。对于大多数毒理学实验室(临床和法医)来说,确定合适的储存条件一直是一个令人关注的问题,滥用药物的稳定性已得到广泛研究。这种关注应扩展到分析化学的其他领域,例如反掺杂控制。在这项工作中,麻黄碱衍生物(麻黄碱,去甲麻黄碱,甲基麻黄碱,伪麻黄碱和去甲伪麻黄碱)和苯丙胺衍生物(苯丙胺,甲基苯丙胺,3,4-亚甲基二氧苯丙胺(MDA)和3,4-亚甲基二氧甲基苯丙胺(MDMA))的稳定性尿液已被研究。准备加标的尿液样品以进行稳定性测试。尿液样品通过GC / NPD或GC / MS进行定量。在开始稳定性研究之前,要验证每批样品的均质性。在不同的储存条件下,对灭菌和非灭菌尿液样品中分析物的稳定性进行了评估。对于长期稳定性测试,无菌尿液样品分别在24个月和6个月内以不同的时间间隔测定4℃和-20℃下储存的尿液中分析物的浓度。对于短期稳定性测试,在37摄氏度下储存7天的液态尿中评估了分析物的浓度。还研究了在无菌尿液中反复冷冻(在-20摄氏度下)和融化(在室温下)的效果,最多进行了三个循环。在任何调查条件下均未观察到被分析物的明显损失。这些结果表明制备包含麻黄碱和苯丙胺衍生物的参比物质用于质量控制目的的可行性。 (c)2006 Elsevier B.V.保留所有权利。

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