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一项使用超高效液相色谱-四极杆飞行时间串联质谱(UPLC-Q-TOF-MS/MS)鉴定阿莫西林-舒巴坦杂合分子在大鼠体内主要代谢产物及其代谢途径的综合研究。

A Comprehensive Study to Identify Major Metabolites of an Amoxicillin-Sulbactam Hybrid Molecule in Rats and Its Metabolic Pathway Using UPLC-Q-TOF-MS/MS.

作者信息

Zhao Fei-Ke, Shi Ren-Bin, Sun Yu-Bin, Yang Shuang-Yun, Chen Liang-Zhu, Fang Bing-Hu

机构信息

National Laboratory of Safety Evaluation (Environmental Assessment) of Veterinary Drugs, South China Agricultural University, Guangzhou 510642, China.

Shenzhen Institute for Drug Control, Shenzhen 518057, China.

出版信息

Metabolites. 2022 Jul 18;12(7):662. doi: 10.3390/metabo12070662.

Abstract

Amoxicillin and sulbactam are widely used compound drugs in animal food. The amoxicillin-sulbactam hybrid molecule can achieve better curative effects through the combination of the two drugs. However, its pharmacokinetic behavior needs to be explored. In this study, a randomized crossover experiment was performed to investigate the metabolism of the novel amoxicillin-sulbactam hybrid molecule in rats after gastric administration. Ultrahigh performance liquid chromatography-quadrupole time-of-flight tandem mass spectrometry (UPLC-Q-TOF-MS/MS) was used to isolate and to identify the metabolites in rats. Amoxicillin, amoxicilloic acid, amoxicillin diketopiperazine, and sulbactam were eventually detected in the plasma, liver, urine, and kidneys; no hybrid molecules and their metabolites were detected in feces. The in vivo metabolism results showed that the hybrid molecule was absorbed into the body in the intestine, producing amoxicillin and sulbactam, then amoxicillin was partially metabolized to amoxicilloic acid and amoxicillin diketopiperazine, which are eventually excreted in the urine by the kidneys. In this study, four major metabolites of the amoxicillin-sulbactam hybrid molecule were identified and their metabolic pathways were speculated, which provided scientific data for understanding the metabolism of the hybrid molecule and for its clinical rational use.

摘要

阿莫西林和舒巴坦是动物食品中广泛使用的复方药物。阿莫西林 - 舒巴坦杂合分子通过两种药物的联合可取得更好的治疗效果。然而,其药代动力学行为有待探索。本研究进行了一项随机交叉实验,以研究新型阿莫西林 - 舒巴坦杂合分子经胃给药后在大鼠体内的代谢情况。采用超高效液相色谱 - 四极杆飞行时间串联质谱(UPLC - Q - TOF - MS/MS)分离并鉴定大鼠体内的代谢产物。最终在血浆、肝脏、尿液和肾脏中检测到了阿莫西林、阿莫西林酸、阿莫西林二酮哌嗪和舒巴坦;在粪便中未检测到杂合分子及其代谢产物。体内代谢结果表明,杂合分子在肠道被吸收进入体内,产生阿莫西林和舒巴坦,然后阿莫西林部分代谢为阿莫西林酸和阿莫西林二酮哌嗪,最终通过肾脏经尿液排出。本研究鉴定了阿莫西林 - 舒巴坦杂合分子的四种主要代谢产物并推测了其代谢途径,为了解杂合分子的代谢及其临床合理应用提供了科学数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61fc/9319383/e5317ce524ed/metabolites-12-00662-g0A1.jpg

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