Comparison of US pharmacopeia simulated intestinal fluid TS (without pancreatin) and phosphate standard buffer pH 6.8, TS of the international pharmacopoeia with respect to their Use in in vitro dissolution testing

Dissolution Technologies

Volumn 11, Issue 2, 2004, Pages 6-10

  Stippler, Erika ^a,b   Kopp, Sabine ^c   Dressman, Jennifer B ^a  

^a GOETHE UNIVERSITY   (Germany)

^b PHAST GmbH   (Germany)

^c WORLD HEALTH ORGANIZATION   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

BUFFER; IBUPROFEN; INDOMETACIN; METRONIDAZOLE;

CALIBRATION; CONTROLLED STUDY; DRUG SOLUBILITY; EXCIPIENT COMPATIBILITY; FILM COATING; IN VITRO STUDY; INTESTINE FLUID; MEDICAL LITERATURE; NOTE; OSMOLARITY; PH; SIMULATION; TITRIMETRY; VALIDATION PROCESS;

EID: 84962046022     PISSN: 1521298X     EISSN: None     Source Type: Journal    
DOI: 10.14227/DT110204P6     Document Type: Note

References (3)

1. United States Pharmacopeia and National Formulary, United States Pharmacopeial Convention Inc., Rockville, MD, USA, 25th Edition (2002) and 26th Edition (2003)
2. The International Pharmacopoeia, WHO, Geneva, Switzerland, 3rd Edition, Volume 1 (1979) and Volume 5 (2003)
3. European Pharmacopoeia, European Directorate for the Quality of Medicines of the Council of Europe (EDQM), Strassbourg, France, 4th Edition (2001)