Drug release from semisolid dosage forms: a comparison of two testing methods-Reference-Cited by-同舟云学术

Drug release from semisolid dosage forms: a comparison of two testing methods

Published:2013-12-13 Issue:3 Volume:20 Page:330-336
ISSN:1083-7450
Container-title:Pharmaceutical Development and Technology
language:en
Short-container-title:Pharmaceutical Development and Technology

Author:

Petró É.,Paál T. L.,Erős I.,Kenneth A. S.,Baki G.,Csóka I.

Publisher

Informa UK Limited

Subject

Pharmaceutical Science,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/10837450.2013.867446

Reference28 articles.

1. Brown CK, Friedel HD, Barker AR, et al. FIP/AAPS Joint Workshop Report: dissolution/in vitro release testing of novel/special dosage forms. Dissolut Technol 2011;18:51–64 and Int J Pharm Sci 2011;73:338–353

2. Barry BW. Drugs and the pharmaceutical sciences: dermatological formulation – percutaneous absorption. New York and Basel: Marcel Dekker; 1983:1-48

3. Techniques For Conducting In Vitro Release Stud ies On Semisolid Formulations

4. Hanson R, Gray V. Handbook of dissolution testing. 3rd ed. Hockessin (DE): Dissolution Technologies; 2004:33-71

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