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首页> 外文期刊>Journal of Analytical Toxicology >Identification of AKB-48 and 5F-AKB-48 Metabolites in Authentic Human Urine Samples Using Human Liver Microsomes and Time of Flight Mass Spectrometry
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Identification of AKB-48 and 5F-AKB-48 Metabolites in Authentic Human Urine Samples Using Human Liver Microsomes and Time of Flight Mass Spectrometry

机译:使用人肝微粒体和飞行时间质谱鉴定真人尿液样品中的AKB-48和5F-AKB-48代谢物

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摘要

The occurrence of structurally related synthetic cannabinoids makes the identification of unique markers of drug intake particularly challenging. The aim of this study was to identify unique and abundant metabolites of AKB-48 and 5F-AKB-48 for toxicological screening in urine. Investigations of authentic urine samples from forensic cases in combination with human liver microsome (HLM) experiments were used for identification of metabolites. HLM incubations of AKB-48 and 5F-AKB-48 along with 35 urine samples from authentic cases were analyzed with liquid chromatography quadrupole tandem time of flight mass spectrometry. Using HLMs 41 metabolites of AKB-48 and 37 metabolites of 5F-AKB-48 were identified, principally represented by hydroxylation but also ketone formation and dealkylation. Monohydroxylated metabolites were replaced by di- and trihydroxylated metabolites within 30 min. The metabolites from the HLM incubations accounted for on average 84% (range, 67-100) and 91% (range, 71-100) of the combined area in the case samples for AKB-48 and 5F-AKB-48, respectively. While defluorinated metabolites accounted for on average 74% of the combined area after a 5F-AKB-48 intake only a few identified metabolites were shared between AKB-48 and 5F-AKB-48, illustrating the need for a systematic approach to identify unique metabolites. HLMs in combination with case samples seem suitable for this purpose.
机译:与结构相关的合成大麻素的出现使得药物摄入独特标记的鉴定特别具有挑战性。这项研究的目的是确定尿液中毒理学筛查的独特且丰富的AKB-48和5F-AKB-48代谢产物。结合人类肝微粒体(HLM)实验,对法医病例的真实尿液样本进行了研究,以鉴定代谢物。使用液相色谱四极杆串联飞行时间质谱分析法对AKB-48和5F-AKB-48的HLM孵育以及35份来自真实病例的尿液样本进行了分析。使用HLM,鉴定出AKB-48的41种代谢物和5F-AKB-48的37种代谢物,主要代表羟基化作用,但也代表酮形成和脱烷基作用。在30分钟内,单羟基化代谢物被二羟基和三羟基化代谢物替代。在AKB-48和5F-AKB-48的案例样本中,HLM孵育产生的代谢物分别平均占合并区域的84%(范围67-100)和91%(范围71-100)。摄入5F-AKB-48后,脱氟代谢物平均占合并区域的74%,AKB-48和5F-AKB-48之间只有少数已鉴定的代谢物共享,这说明需要系统的方法来鉴定独特的代谢物。结合案例样本的HLM似乎适用于此目的。

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