Faculdade de Farmácia, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-019 Lisboa, Portugal.
Faculdade de Farmácia, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-019 Lisboa, Portugal; iMed.ULisboa (Research Institute for Medicines), Faculdade de Farmácia, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal.
J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Nov 30;1159:122340. doi: 10.1016/j.jchromb.2020.122340. Epub 2020 Aug 25.
N-ethylhexedrone (NEH) and buphedrone (BUPH) are synthetic drugs structurally related to natural cathinone. These synthetic cathinones (SC) are members of the heterogenous family of new psychoactive substances (NPS), which have caused major concern in scientific and forensic communities over the past years, due to their widespread consume. Thus, there is a constant need for monitoring the use of these new substances and gather knowledge on their metabolism and excretion profiles, in order to try to identify markers of NPS consumption. This study aimed at the identification and quantification of NEH, BUPH and selected phase I metabolites using HPLC-MS/MS. NEH, BUPH and some related metabolites were synthesized in-house and quantified in 24 h mice urine, following single dose administration of each drug (64 mg kg, i.p.). NEH and BUPH were quantified in mice urine at 58.3 ± 14.4 and 146.2 ± 14.9 µg mL, respectively. Similar metabolic pathways were observed for both drugs. Among the metabolites studied, the most excreted ones derived from N-dealkylation of either NEH or BUPH (at around 80 µg mL of urine). Other metabolites resulting from ketone reduction and ketone reduction combined with N-dealkylation or 4-aryl hydroxylation (detected for the first time in non-ring substituted SC) were also identified and quantified. Urine samples were screened using liquid chromatography-high resolution mass spectrometry and various phase II metabolites, including N-acetylated, glucuronides and dicarboxylic acid conjugates were tentatively identified, some of them for the first time. This work is a contribution to the identification of metabolites from SC that can become potential markers to estimate drug consumption.
N-乙基己基酮(NEH)和丁基芬(BUPH)是与天然卡他碱结构相关的合成药物。这些合成卡他碱(SC)是新型精神活性物质(NPS)异质家族的成员,由于其广泛消费,近年来在科学和法医学界引起了极大关注。因此,需要不断监测这些新物质的使用情况,并积累有关其代谢和排泄特征的知识,以便尝试识别 NPS 消费的标志物。本研究旨在使用 HPLC-MS/MS 鉴定和定量 NEH、BUPH 和选定的 I 相代谢物。NEH、BUPH 和一些相关代谢物在内部合成,并在单次给药(64mgkg,ip)后定量分析 24 小时小鼠尿液。在小鼠尿液中定量检测到 NEH 和 BUPH 的浓度分别为 58.3±14.4 和 146.2±14.9μgmL。观察到两种药物具有相似的代谢途径。在所研究的代谢物中,最主要的代谢物是来自 NEH 或 BUPH 的 N-脱烷基化产物(约 80μgmL 的尿液)。还鉴定和定量了其他代谢物,这些代谢物是由酮还原和酮还原与 N-脱烷基化或 4-芳基羟化结合产生的(首次在非环取代的 SC 中检测到)。使用液相色谱-高分辨率质谱对尿液样本进行筛查,初步鉴定了各种 II 相代谢物,包括 N-乙酰化、葡萄糖醛酸和二羧酸缀合物,其中一些是首次鉴定。这项工作是对 SC 代谢物的鉴定的贡献,这些代谢物可能成为估计药物消费的潜在标志物。