A Pregnancy Physiologically Based Pharmacokinetic Model Verified For Different Drugs Metabolized And Eliminated Via Various Pathways

Dallmann Andre; Ince Ibrahim; Solodenko Juri; Coboeken Katrin; Hempel Georg; Eissing Thomas

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A Pregnancy Physiologically Based Pharmacokinetic Model Verified For Different Drugs Metabolized And Eliminated Via Various Pathways

机译：妊娠生理基础的药代动力学模型用于通过各种途径代谢和消除的不同药物

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来源
《Journal of pharmacokinetics and pharmacodynamics》 |2017年第suppla期|共2页
作者
Dallmann Andre; Ince Ibrahim; Solodenko Juri; Coboeken Katrin; Hempel Georg; Eissing Thomas;
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作者单位

Univ Munster Munster Germany;

Bayer AG Clin Pharmacometr Leverkusen Germany;

Bayer AG Clin Pharmacometr Leverkusen Germany;

Bayer AG Clin Pharmacometr Leverkusen Germany;

Univ Munster Munster Germany;

Bayer AG Clin Pharmacometr Leverkusen Germany;

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原文格式 PDF
正文语种 eng
中图分类药学;
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1. A Pregnancy Physiologically Based Pharmacokinetic Model Verified For Different Drugs Metabolized And Eliminated Via Various Pathways [J] . Dallmann Andre, Ince Ibrahim, Solodenko Juri, Journal of pharmacokinetics and pharmacodynamics . 2017,第Suppla期

机译：妊娠生理基础的药代动力学模型用于通过各种途径代谢和消除的不同药物
2. A pregnancy physiologically based pharmacokinetic (p-PBPK) model for disposition of drugs metabolized by CYP1A2, CYP2D6 and CYP3A4 [J] . GaohuaL., AbduljalilK., JameiM., British Journal of Clinical Pharmacology . 2012,第5期

机译：基于妊娠生理学的药代动力学（p-PBPK）模型，用于处理被CYP1A2，CYP2D6和CYP3A4代谢的药物
3. A pregnancy physiologically based pharmacokinetic (p-PBPK) model for disposition of drugs metabolized by CYP1A2, CYP2D6 and CYP3A4 [J] . Lu Gaohua, Khaled Abduljalil, Masoud Jamei, British journal of clinical pharmacology . 2012,第5期

机译：基于妊娠生理学的药代动力学（p-PBPK）模型，用于处理被CYP1A2，CYP2D6和CYP3A4代谢的药物
4. Physiologically Based Pharmacokinetic Model of Midazolam Disposition during Pregnancy [C] . Marilee A. Andrew, Mary F. Hebert, Paolo Vicini Annual International Conference of the IEEE Engineering in Medicine and Biology Society . 2008

机译：怀孕期间咪达唑仑部处置的生理基础药代动力学模型
5. Applications of Physiologically Based Pharmacokinetic Modelling to Prediction of the Likelihood of Metabolic Drug Interactions in Paediatric Population and Studying Disparities in Pharmacokinetics Between Children and Adults [D] . Salem, Farzaneh. 2014

机译：基于生理的药代动力学模型在小儿人群中代谢药物相互作用的可能性预测和研究儿童与成人之间药代动力学差异的应用
6. A pregnancy physiologically based pharmacokinetic (p-PBPK) model for disposition of drugs metabolized by CYP1A2 CYP2D6 and CYP3A4 [O] . Lu Gaohua, Khaled Abduljalil, Masoud Jamei, 2012

机译：基于妊娠生理学的药代动力学（p-PBPK）模型用于处理被CYP1A2CYP2D6和CYP3A4代谢的药物
7. A pregnancy physiologically based pharmacokinetic (p-PBPK) model for disposition of drugs metabolized by CYP1A2, CYP2D6 and CYP3A4 [O] . Gaohua, Lu, Abduljalil, Khaled, Jamei, Masoud, 2012

机译：基于妊娠生理学的药代动力学（p-pBpK）模型，用于处置由CYp1a2，CYp2D6和CYp3a4代谢的药物

A Pregnancy Physiologically Based Pharmacokinetic Model Verified For Different Drugs Metabolized And Eliminated Via Various Pathways

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