CYP2C19型
奥美拉唑
药品
药理学
体外
药物相互作用
伏立康唑
化学
医学
生物
微生物学
细胞色素P450
内科学
生物化学
新陈代谢
抗真菌
出处
期刊:Xenobiotica
[Taylor & Francis]
日期:2024-10-24
卷期号:: 1-29
被引量:1
标识
DOI:10.1080/00498254.2024.2421513
摘要
The drug-drug interaction (DDI) and CYP2C19 genetic variation can lead to a high blood concentration of voriconazole. CYP2C19 is a highly genetically polymorphic enzyme, and CYP2C19*2 is more frequent among Asians associated with reduced metabolism of drugs. Clinical study found that co-administration with omeprazole significantly increased voriconazole concentrations and there was an additive effect in CYP2C19*2 allele.CYP2C19 rs4244285 (681G > A) is the key polymorphism of CYP2C19*2 allele. This study aims to describe the
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