首页|经CYP450酶代谢的常见阿片类药物比较

经CYP450酶代谢的常见阿片类药物比较

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目的 总结常见阿片类药物羟考酮、美沙酮、曲马多和丁丙诺啡涉及细胞色素P450(CYP450)酶的代谢过程。方法 采用计算机检索PubMed自建库起至 2024 年 3 月关于羟考酮、美沙酮、曲马多和丁丙诺啡等阿片类药物经CYP450 酶的代谢研究,以及CYP450 酶涉及的药物相互作用。结果 CYP450 酶是羟考酮、美沙酮、曲马多和丁丙诺啡阿片类药物代谢过程中最重要的酶。CYP3A4 和CYP2D6 不仅参与大多数阿片类药物代谢,还参与大量其他药物的代谢,阿片类药物在用药过程中易与其他药物发生相互作用。结论 了解阿片类药物在肝脏中的代谢,以及药物间相互作用涉及重叠的药效动力学、药代动力学,可避免用药过程中可能发生的药品不良反应。
Comparison of Common Opioids Metabolized by CYP450 Enzymes
Objective To summarize the cytochrome P450(CYP450)enzyme metabolism processes involved in common opioid drugs such as oxycodone,methadone,tramadol,and buprenorphine.Methods PubMed was searched from its inception to March 2024 for studies on the metabolism of opioids such as oxycodone,methadone,tramadol and buprenorphine via the CYP450 enzyme,as well as drug-drug interactions involved in the CYP450 enzyme.Results CYP450 enzyme was the most important enzyme in the metabolism of opioid drugs such as oxycodone,methadone,tramadol,and buprenorphine.CYP3A4 and CYP2D6 were not only involved in the metabolism of most opioid but also a large number of other drugs,and opioid drugs were prone to have drug-drug interactions with other drugs during the medication.Conclusion Knowledge of the metabolism of opioids in the liver,and the overlapping pharmacodynamics and pharmacokinetics involved in drug-drug interactions can help to circumvent possible adverse drug reactions during the medication.

opioidscytochrome P450 enzymemetabolismadverse drug reactionsdrug-drug interactions

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重庆市食品药品检验检测研究院·国家药品监督管理局麻醉精神药品质量监测重点实验室,重庆 401121

阿片类药物 细胞色素P450酶 代谢 药品不良反应 药物相互作用

重庆市科研机构绩效激励引导专项

CQIFDC-YJKT-2021-12

2024

中国药业
重庆市食品药品监督管理局

中国药业

CSTPCD
影响因子:1.369
ISSN:1006-4931
年,卷(期):2024.33(9)
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