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Correction to “Plasma and Hepatic Concentrations of Chemicals after Virtual Oral Administrations Extrapolated Using Rat Plasma Data and Simple Physiologically Based Pharmacokinetic Models”

机译：用大鼠等离子体数据和简单的生理基于药代动力学模型改进“虚拟口腔施用后的血浆和肝浓度的化学品。

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Yusuke Kamiya; Shohei Otsuka; Tomonori Miura; Hiroka Takaku; Rio Yamada; Mayuko Nakazato; Hitomi Nakamura; Sawa Mizuno; Fumiaki Shono; Kimito Funatsu; Hiroshi Yamazaki;
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1. Plasma and Hepatic Concentrations of Chemicals after Virtual Oral Administrations Extrapolated Using Rat Plasma Data and Simple Physiologically Based Pharmacokinetic Models (vol 32, pg 211, 2019) [J] . Kamiya Yusuke, Otsuka Shohei, Miura Tomonori, Chemical research in toxicology . 2019,第4期

机译：虚拟口腔施用后的血浆和肝浓度的化学物质使用大鼠等离子体数据和简单的生理基于药代动力学模型外推外推出（Vol 32，PG 211,2019）
2. Plasma and Hepatic Concentrations of Chemicals after Virtual Oral Administrations Extrapolated Using Rat Plasma Data and Simple Physiologically Based Pharmacokinetic Models [J] . Kamiya Yusuke, Otsuka Shohei, Miura Tomonori, Chemical research in toxicology . 2019,第1期

机译：使用大鼠等离子体数据和简单的生理基础药代动力学模型在虚拟口腔给药后的血浆和肝浓度的化学品。
3. Blood Concentrations of 1,4-Dioxane in Humans after Oral Administration Extrapolated from In Vivo Rat Pharmacokinetics, In Vitro Human Metabolism, and Physiologically Based Pharmacokinetic Modeling [J] . Ryohji Takano, Norie Murayama, Kana Horiuchi, Journal of health science. . 2010,第5期

机译：从体内大鼠药代动力学，人体体外代谢和基于生理学的药代动力学模型推断的口服给药后，人体中1,4-二恶烷的血药浓度
4. Self-Regulating Physiologically Based Pharmacokinetic Model and Creation of Drug Concentration Profiles in Plasma and Tissues [C] . Stanislav Polinkevych International Conference on Bioinformatics Computational Biology . 2011

机译：基于生理的药代动力学模型和血浆和组织中药物浓度谱的创造
5. Evaluation of the pharmacokinetic-pharmacodynamic relationship, metabolism and plasma protein binding of the novel antitumor agent, 2-methoxyestradiol (2ME2), following oral administration in patients with solid tumors. [D] . Lakhani, Nehal Jagdish. 2005

机译：实体瘤患者口服后评估新型抗肿瘤药2-甲氧基雌二醇（2ME2）的药代动力学与药效关系，代谢和血浆蛋白结合。
6. Comprehensive characterization of the chemical constituents in Yiganmingmu oral liquid and the absorbed prototypes in cynomolgus monkey plasma after oral administration by UPLC-Q-TOF-MS based on the self built components database [O] . Wei Wei, Siwei Li, Linyou Cheng, 2021

机译：基于自置组件数据库通过UPLC-Q-TOF-MS在口服给药后yiganmingmu口服液体和吸收原型的综合表征。
7. Human Plasma Concentrations of Tolbutamide and Acetaminophen Extrapolated from in vivo Animal Pharmacokinetics Using in vitro Human Hepatic Clearances and Simple Physiologically Based Pharmacokinetic Modeling for Radio-labeled Microdose Clinical Studies [O] . Hiroshi YAMAZAKI, Eriko KUNIKANE, Sayako NISHIYAMA, 2015

机译：人体血浆浓度与乙酰丁胺烯烃的甲醛和乙酰氨基酚在体内的甲酰胺中外推，使用在体外的人肝脏间隙和用于无线标记微孔临床研究的简单生理学药代动力学建模
8. Pralidoxime Methane Sulfonate: Plasma Levels and Pharmacokinetics in Man After Oral Administration of a New Preparation [R] . Sidell, F. R., Groff, W. A., Kaminskis, A. 1972

机译：pralidoxime甲烷磺酸盐：口服新制剂后人体血浆水平和药代动力学

Correction to “Plasma and Hepatic Concentrations of Chemicals after Virtual Oral Administrations Extrapolated Using Rat Plasma Data and Simple Physiologically Based Pharmacokinetic Models”

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