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A Novel In Vitro Pharmacokinetic/Pharmacodynamic Model Based on Two- Compartment Open Model Used to Simulate Serum Drug Concentration-Time Profiles

机译：基于双室开放模型的新型体外药代动力学/药效学模型，用于模拟血清药物浓度 - 时间曲线

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Tsutomu Tomita; Yuko Ohara-nemoto; Hitomi Moriyama; Ayako Ozawa; Yoshifumi Takeda; Ken Kikuchi;
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年度 2015
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1. A novel in vitro pharmacokinetic/pharmacodynamic model based on two-compartment open model used to simulate serum drug concentration-time profiles. [J] . Tomita T, Ohara-Nemoto Y, Moriyama H, Microbiology and Immunology . 2007,第5期

机译：基于两室开放模型的新型体外药代动力学/药效学模型，用于模拟血清药物浓度-时间曲线。
2. Susceptibility breakpoints for amphotericin B and Aspergillus species in an in Vitro pharmacokinetic-pharmacodynamic model simulating free-drug concentrations in human serum [J] . ElefantiA., MoutonJ.W., VerweijP.E., Antimicrobial agents and chemotherapy. . 2014,第4期

机译：模拟人血清中游离药物浓度的体外药代动力学-药效学模型中两性霉素B和曲霉菌种的敏感性断点
3. Susceptibility breakpoints for amphotericin B and Aspergillus species in an in Vitro pharmacokinetic-pharmacodynamic model simulating free-drug concentrations in human serum [J] . ElefantiA., MoutonJ.W., VerweijP.E., Antimicrobial agents and chemotherapy. . 2014,第4期

机译：模拟人血清中游离药物浓度的体外药代动力学-药效学模型中两性霉素B和曲霉菌种的敏感性断点
4. A Fuzzy Neartude Based Approach to Simulate the Two-Compartment Pharmacokinetic Model [C] . Lei Zhao, Xinling Shi, Yufeng Zhang, International conference on information technology and software engineering;ITSE2012 . 2013

机译：基于模糊Nordude的两室药代动力学模型仿真方法
5. In Vitro-In Vivo Assessment of Repaglinide Metabolism and Drug-Drug Interactions: Towards a Physiologically-Based Pharmacokinetic Model [D] . Thule S?ll, Carolina Maria. 2013

机译：瑞格列奈代谢和药物-药物相互作用的体外评估：建立基于生理学的药代动力学模型
6. Susceptibility Breakpoints for Amphotericin B and Aspergillus Species in an In Vitro Pharmacokinetic-Pharmacodynamic Model Simulating Free-Drug Concentrations in Human Serum [O] . A. Elefanti, J. W. Mouton, P. E. Verweij, 2014

机译：两性霉素B和曲霉菌种在模拟人体血清中自由药物浓度的体外药代动力学-药效学模型中的敏感性断点
7. A novel in vitro pharmacokinetic/pharmacodynamic model based on two-compartment open model used to simulate serum drug concentration-time profiles. [O] . Tomita Tsutomu, Ohara-Nemoto Yuko, Moriyama Hitomi, 2007

机译：基于双室开放模型的新型体外药代动力学/药效学模型，用于模拟血清药物浓度 - 时间曲线。

A Novel In Vitro Pharmacokinetic/Pharmacodynamic Model Based on Two- Compartment Open Model Used to Simulate Serum Drug Concentration-Time Profiles

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