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Conference Report

In Vitro and In Vivo Evaluation of Drug Release from Semisolid Dosage Forms

1
Department of Drug Regulatory Affairs, University of Szeged, Szeged, Hungary
2
Department of Pharmacodynamics and Biopharmacy, University of Szeged, Szeged, Hungary
3
Department of Pharmaceutical Technology, University of Szeged, Szeged, Hungary
*
Author to whom correspondence should be addressed.
Submission received: 12 July 2010 / Accepted: 12 July 2010 / Published: 12 July 2010

Abstract

Semisolid products are 8–10% of dosage forms, but – in contrast with the solid dosage forms – we do not have any validated method for their drug release in any Pharmacopoeia. [...]

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MDPI and ACS Style

PETRÓ, É.; CSÓKA, I.; BALOGH, Á.; BLAZSÓ, G.; ERŐS, I. In Vitro and In Vivo Evaluation of Drug Release from Semisolid Dosage Forms. Sci. Pharm. 2010, 78, 597. https://0-doi-org.brum.beds.ac.uk/10.3797/scipharm.cespt.8.PDD08

AMA Style

PETRÓ É, CSÓKA I, BALOGH Á, BLAZSÓ G, ERŐS I. In Vitro and In Vivo Evaluation of Drug Release from Semisolid Dosage Forms. Scientia Pharmaceutica. 2010; 78(3):597. https://0-doi-org.brum.beds.ac.uk/10.3797/scipharm.cespt.8.PDD08

Chicago/Turabian Style

PETRÓ, É., I. CSÓKA, Á. BALOGH, G. BLAZSÓ, and I. ERŐS. 2010. "In Vitro and In Vivo Evaluation of Drug Release from Semisolid Dosage Forms" Scientia Pharmaceutica 78, no. 3: 597. https://0-doi-org.brum.beds.ac.uk/10.3797/scipharm.cespt.8.PDD08

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