药代动力学

The pharmacokinetics of the drug were studied to determine its absorption, distribution, metabolism, and excretion in the body.
研究该药物的药代动力学以确定其在体内的吸收、分布、代谢和排泄情况。
A key aspect of drug development involves understanding the pharmacokinetics of the compound in humans.
药物研发的关键环节之一是了解化合物在人体内的药代动力学。
Pharmacokinetic properties of the new antibiotic allowed for more effective dosing intervals.
新型抗生素的药代动力学特性使得更有效的用药间隔成为可能。
The pharmacokinetics of the drug can be influenced by factors such as age, weight, and liver function.
药物的药代动力学可以受到年龄、体重和肝功能等因素的影响。
This study aims to investigate the pharmacokinetics and pharmacodynamics of the novel anticoagulant in rats.
本研究旨在探究新型抗凝剂在大鼠体内的药代动力学和药效动力学。
Poor pharmacokinetic profiles can lead to inadequate therapeutic effects or increased risk of adverse reactions.
较差的药代动力学特征可能导致治疗效果不足或增加不良反应的风险。
Understanding the pharmacokinetics is crucial for predicting drug-drug interactions and optimizing patient therapy.
理解药物的药代动力学对于预测药物相互作用及优化患者治疗至关重要。
The pharmacokinetic parameters of the drug were determined using non-compartmental analysis.
采用非房室分析方法确定了药物的药代动力学参数。
Due to its favorable pharmacokinetic characteristics, the drug can be administered orally or intravenously.
由于其良好的药代动力学特性，该药物既可口服也可静脉给药。
Genetic polymorphisms can significantly impact the inter-individual variability in pharmacokinetics among patients.
遗传多态性可能会显著影响患者间的药代动力学个体差异。