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采用液相色谱-串联质谱法对 7-和 8-羟基唑吡坦进行定性分析,并在死后尿液中发现新型唑吡坦代谢物。

Qualitative analysis of 7- and 8-hydroxyzolpidem and discovery of novel zolpidem metabolites in postmortem urine using liquid chromatography-tandem mass spectrometry.

机构信息

Department of Legal Medicine, Nippon Medical School, 1715 Kamagari, Inzai, Chiba, 270-1694, Japan.

National Research Institute of Police Science, 6-3-1 Kashiwanoha, Kashiwa, Chiba, 277-0882, Japan.

出版信息

Forensic Toxicol. 2022 Jul;40(2):263-277. doi: 10.1007/s11419-021-00611-9. Epub 2022 Jan 4.

Abstract

PURPOSE

Zolpidem (ZOL) is a hypnotic sometimes used in drug-facilitated crimes. Understanding ZOL metabolism is important for proving ZOL intake. In this study, we synthesized standards of hydroxyzolpidems with a hydroxy group attached to the pyridine ring and analyzed them to prove their presence in postmortem urine. We also searched for novel ZOL metabolites in the urine sample using liquid chromatography-triple quadrupole mass spectrometry (LC-QqQMS) and liquid chromatography-quadrupole time-of-flight mass spectrometry (LC-QqTOFMS).

METHODS

7- and 8-Hydroxyzolpidem (7OHZ and 8OHZ, respectively) were synthesized and analyzed using LC-QqQMS. Retention times were compared between the synthetic standards and extracts of postmortem urine. To search for novel ZOL metabolites, first, the urine extract was analyzed with data-dependent acquisition, and the peaks showing the characteristic fragmentation pattern of ZOL were selected. Second, product ion spectra of these peaks at various collision energies were acquired and fragments that could be used for multiple reaction monitoring (MRM) were chosen. Finally, MRM parameters were optimized using the urine extract. These peaks were also analyzed using LC-QqTOFMS.

RESULTS

The presence of 7OHZ and 8OHZ in urine was confirmed. The highest peak among hydroxyzolpidems was assigned to 7OHZ. The novel metabolites found were zolpidem dihydrodiol and its glucuronides, cysteine adducts of ZOL and dihydro(hydroxy)zolpidem, and glucuronides of hydroxyzolpidems.

CONCLUSIONS

The presence of novel metabolites revealed new metabolic pathways, which involve formation of an epoxide on the pyridine ring as an intermediate.

摘要

目的

唑吡坦(zolpidem,ZOL)是一种催眠药,有时用于药物辅助犯罪。了解 ZOL 的代谢对于证明 ZOL 的摄入非常重要。在这项研究中,我们合成了带有吡啶环上羟基的羟唑吡坦标准品,并对其进行分析,以证明其存在于死后尿液中。我们还使用液相色谱-三重四极杆质谱(LC-QqQMS)和液相色谱-四极杆飞行时间质谱(LC-QqTOFMS)在尿液样本中寻找新型 ZOL 代谢物。

方法

合成了 7-和 8-羟唑吡坦(7OHZ 和 8OHZ),并使用 LC-QqQMS 进行分析。比较了合成标准品与死后尿液提取物的保留时间。为了寻找新型 ZOL 代谢物,首先,使用数据依赖采集对尿液提取物进行分析,选择显示 ZOL 特征碎片模式的峰。然后,在不同碰撞能量下获取这些峰的产物离子谱,并选择可用于多重反应监测(MRM)的片段。最后,使用尿液提取物优化了 MRM 参数。这些峰也使用 LC-QqTOFMS 进行了分析。

结果

证实了尿液中 7OHZ 和 8OHZ 的存在。羟唑吡坦中最高的峰被分配给 7OHZ。发现的新型代谢物有唑吡坦二氢二醇及其葡糖苷酸、ZOL 和二氢(羟基)唑吡坦的半胱氨酸加合物,以及羟唑吡坦的葡糖苷酸。

结论

新型代谢物的存在揭示了新的代谢途径,其中涉及作为中间体的吡啶环上形成环氧化物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca53/9715527/7d3f2beb0bc8/11419_2021_611_Fig1_HTML.jpg

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