Examples of developing in vitro-in vivo relationships.
作者信息
Butler J
机构信息
IVIVR Cooperative Working Group, Elan Corporation, Athlone, Ireland.
出版信息
Adv Exp Med Biol. 1997;423:93-110. doi: 10.1007/978-1-4684-6036-0_8.
PMID:9269486
Abstract
摘要
相似文献
1
Examples of developing in vitro-in vivo relationships.
Adv Exp Med Biol. 1997;423:93-110. doi: 10.1007/978-1-4684-6036-0_8.
2
PBPK models for the prediction of in vivo performance of oral dosage forms.用于预测口服剂型体内性能的生理药代动力学（PBPK）模型。
Eur J Pharm Sci. 2014 Jun 16;57:300-21. doi: 10.1016/j.ejps.2013.09.008. Epub 2013 Sep 21.
3
[Pharmacokinetics parameters of the gastrointestinal absorption of drugs (author's transl)].药物胃肠道吸收的药代动力学参数（作者译）
J Pharm Belg. 1975 May-Jun;30(3):239-72.
4
Pharmacokinetic simulation of biowaiver criteria: the effects of gastric emptying, dissolution, absorption and elimination rates.生物豁免标准的药代动力学模拟：胃排空、溶解、吸收和消除速率的影响。
Eur J Pharm Sci. 2007 Feb;30(2):155-66. doi: 10.1016/j.ejps.2006.10.011. Epub 2006 Nov 11.
5
Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. I. Theoretical considerations and discussion of the literature.通过固溶体和低共熔混合物提高药物的溶解速率和胃肠道吸收。I. 理论考量及文献讨论
J Pharm Sci. 1965 Aug;54(8):1145-8. doi: 10.1002/jps.2600540810.
6
The use of physical and animal models to assess bioavailability.使用物理模型和动物模型来评估生物利用度。
Pharmacology. 1972;8(1):55-101. doi: 10.1159/000136327.
7
Confounding factors for sex differences in pharmacokinetics and pharmacodynamics: focus on dosing regimen, dosage form, and formulation.药代动力学和药效学中性别差异的混杂因素：关注给药方案、剂型和制剂。
Clin Pharmacol Ther. 2005 Oct;78(4):322-9. doi: 10.1016/j.clpt.2005.06.012.
8
Oral biopharmaceutics tools - time for a new initiative - an introduction to the IMI project OrBiTo.口服生物药剂学工具——开启新计划的时机——IMI项目OrBiTo介绍
Eur J Pharm Sci. 2014 Jun 16;57:292-9. doi: 10.1016/j.ejps.2013.10.012. Epub 2013 Nov 1.
9
Characterising the behaviour of poorly water soluble drugs in the intestine: application of biorelevant media for solubility, dissolution and transport studies.表征肠道中难溶性药物的行为：生物相关介质在溶解度、溶解和传输研究中的应用。
J Pharm Pharmacol. 2010 Nov;62(11):1656-68. doi: 10.1111/j.2042-7158.2010.01023.x.
10
Predicting human drug pharmacokinetics from in vitro permeability using an absorption-disposition model.使用吸收-处置模型从体外通透性预测人体药物药代动力学。
J Pharm Sci. 2007 Aug;96(8):2161-70. doi: 10.1002/jps.20866.
Zotero 插件