Dissolution study of active pharmaceutical ingredients using the flow through apparatus Usp 4

Dissolution Technologies

Volumn 12, Issue 2, 2005, Pages 23-25

  Beyssac, E ^a   Lavigne, J ^a  

^a Biopharmaceutics Department   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLSALICYLIC ACID; THEOPHYLLINE;

ANALYTIC METHOD; ANALYTICAL EQUIPMENT; ARTICLE; COMPARATIVE STUDY; DISSOLUTION; DISSOLUTION MEDIA; DISSOLUTION RATE CONSTANT; DISSOLUTION TEST; DRUG CAPSULE; DRUG DISTRIBUTION; DRUG RELEASE; DRUG SOLUBILITY; FLOW RATE; FLOW THROUGH APPARATUS USP 4; IN VITRO STUDY; PARTICLE SIZE; POWDER; QUALITY CONTROL; REPRODUCIBILITY; TABLET; ULTRAVIOLET SPECTROPHOTOMETRY;

EID: 33745812027     PISSN: 1521298X     EISSN: None     Source Type: Journal    
DOI: 10.14227/DT120205P23     Document Type: Article

References (5)

1. Guidance for Industry: Dissolution Testing of Immediate Release Solid Oral Dosage Forms, U. S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), August 1997
2. Guidance for Industry: Extended Release Oral Dosage Forms: Development, Evaluation, and Application of In Vitro/In Vivo Correlations, U. S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), September 1997
3. United States Pharmacopeia and National Formulary, United States Pharmacopeia Convention Inc., Rockville, MD, USA, 26th Edition, 2003
4. European Pharmacopeia, Council of Europe, Strasbourg, France, 2001
5. Amiji, M. A., Sandmann B. J., Applied physical pharmacy, McGraw-Hill Companies; USA, 2003