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食欲素受体拮抗剂苏沃雷生及其代谢产物的尿排泄情况

Urinary excretion profiles of the orexin receptor antagonist suvorexant and its metabolites.

作者信息

Wada Misato, Kamata Hiroe, Shima Noriaki, Nitta Atsushi, Kakehashi Hidenao, Fujii Shihoko, Matsuta Shuntaro, Kamata Tooru, Katagi Munehiro, Nishioka Hiroshi

机构信息

Forensic Science Laboratory, Osaka Prefectural Police Head Quarters, 1-3-18, Hommachi, Chuo-Ku, Osaka, 541-0053, Japan.

出版信息

Forensic Toxicol. 2025 Jul;43(2):179-189. doi: 10.1007/s11419-024-00706-z. Epub 2024 Dec 18.

Abstract

PURPOSE

Suvorexant is an orexin receptor antagonist used in the treatment of insomnia. In this study, we investigated the urinary excretion profiles of suvorexant and its major metabolites, including conjugates, to obtain fundamental information for proving exposure to suvorexant in criminal cases.

METHODS

Urine specimens were collected from three subjects for maximum 168 h after a single oral ingestion of suvorexant (10 mg), and suvorexant and its metabolites in urine were determined using liquid chromatography-tandem mass spectrometry with a C18 semi-micro column.

RESULTS

The carboxylic and hydroxy metabolites (M4 and M9) were identified with authentic standards synthesized in our laboratory, and their glucuronides and other hydroxy metabolites (M8 and M10) were tentatively detected based on measured exact masses and product ion spectra of them. Suvorexant, M4 and M9 would be detectable for 20-34 h, 6-7 days and 42-61 h after intake, respectively. The quantitative results demonstrated that the molar ratios of accumulated amounts of M4 and M9 including their glucuronides excreted in urine to dose ranged about 2.6-6.2% and 0.37-0.51%, respectively, while that of the unchanged parent was much lower (0.011-0.013%). The ratios of the amount of glucuronide to the total amount of M4 and M9 excreted in urine was less than 10% and approximately 90%, respectively.

CONCLUSIONS

The urinary excretion profiles indicated that M4 and M9 would be effective indicators for proving suvorexant intake, and M4 could be detected until one week after intake even without enzymatic hydrolysis (limit of detection: 0.05 ng/mL).

摘要

目的

苏沃雷生是一种用于治疗失眠的食欲素受体拮抗剂。在本研究中,我们调查了苏沃雷生及其主要代谢物(包括结合物)的尿排泄情况,以获取在刑事案件中证明苏沃雷生暴露的基础信息。

方法

三名受试者单次口服苏沃雷生(10毫克)后,在长达168小时内收集尿液样本,使用配备C18半微柱的液相色谱-串联质谱法测定尿液中的苏沃雷生及其代谢物。

结果

通过我们实验室合成的标准品鉴定出羧酸和羟基代谢物(M4和M9),并根据它们的精确质量和产物离子光谱初步检测到它们的葡萄糖醛酸苷和其他羟基代谢物(M8和M10)。摄入后,苏沃雷生、M4和M9分别在20 - 34小时、6 - 7天和42 - 61小时内可被检测到。定量结果表明,尿液中排泄的包括葡萄糖醛酸苷的M4和M9累积量与剂量的摩尔比分别约为2.6 - 6.2%和0.37 - 0.51%,而未变化的母体的摩尔比则低得多(0.011 - 0.013%)。尿液中葡萄糖醛酸苷与排泄的M4和M9总量的比例分别小于10%和约90%。

结论

尿排泄情况表明,M4和M9将是证明苏沃雷生摄入的有效指标,即使不进行酶水解(检测限:0.05纳克/毫升),M4在摄入后一周内仍可被检测到。

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