Characterising Drug Release from Immediate-Release Formulations of a Poorly Soluble Compound, Basmisanil, Through Absorption Modelling and Dissolution Testing-Reference-Cited by-同舟云学术

Characterising Drug Release from Immediate-Release Formulations of a Poorly Soluble Compound, Basmisanil, Through Absorption Modelling and Dissolution Testing

Published:2017-02-24 Issue:3 Volume:19 Page:827-836
ISSN:1550-7416
Container-title:The AAPS Journal
language:en
Short-container-title:AAPS J

Author:

Stillhart Cordula,Parrott Neil J.,Lindenberg Marc,Chalus Pascal,Bentley Darren,Szepes Anikó

Publisher

Springer Science and Business Media LLC

Subject

Pharmaceutical Science

Link

http://link.springer.com/content/pdf/10.1208/s12248-017-0060-1.pdf

Reference27 articles.

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4. Eaga C, Mantri S, Malayandi R, Kondamudi PK, Chakraborty S, Raju SVN, et al. Establishing postprandial bio-equivalency and IVIVC for generic metformin sustained release small sized tablets. J Pharm Investig. 2014;44(3):197–204. doi: 10.1007/s40005-013-0115-y .

5. Ilic M, Duris J, Kovacevic I, Ibric S, Parojcic J. In vitro-in silico-in vivo drug absorption model development based on mechanistic gastrointestinal simulation and artificial neural networks: nifedipine osmotic release tablets case study. Eur J Pharm Sci. 2014;62:212–8. doi: 10.1016/j.ejps.2014.05.030 .

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