Predicting in vivo absorption behavior of oral modified release dosage forms containing pH-dependent poorly soluble drugs using a novel pH-adjusted biphasic in vitro dissolution test

Author:

Heigoldt Ulrich,Sommer Florian,Daniels Rolf,Wagner Karl-Gerhard

Publisher

Elsevier BV

Subject

Pharmaceutical Science,General Medicine,Biotechnology

Reference37 articles.

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2. Current perspectives in dissolution testing of conventional and novel dosage forms;Azarmi;Int. J. Pharm.,2007

3. FIP/AAPS guidelines for dissolution/in vitro release testing of novel/special dosage forms;Siewert;Pharm. Ind.,2003

4. Development of dissolution tests for oral extended-release products;Jorgensen;Pharm. Sci. Technol. Today,1998

5. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability;Amidon;Pharm. Res.,1995

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