Evaluation of induced variance of physical parameters on the calibrated USP dissolution apparatus 1 and 2

Dissolution Technologies

Volumn 12, Issue 1, 2005, Pages 28-31

  Crist, Bryan ^a   Spisak, Dan ^a  

^a Varian Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PREDNISONE; SALICYLIC ACID;

ANALYTICAL EQUIPMENT; ARTICLE; CALIBRATION; CALIBRATOR; DISSOLUTION APPARATUS; DRUG RELEASE; PHYSICAL PARAMETERS; TABLET; TABLET DISINTEGRATION; TEMPERATURE; VIBRATION;

EID: 41549168738     PISSN: 1521298X     EISSN: None     Source Type: Journal    
DOI: 10.14227/DT120105P28     Document Type: Article

References (5)

1. Dissolution Testing of Immediate Release Solid Oral Dosage forms, FDA Guidance for Industry; Center for Drug Evaluation and Research, Aug 1997, p. A-2
2. USP 28/NF 23, United States Pharmacopeia / National Formulary, Rockville, MD, Official January 1, 2005
3. USP Dissolution Calibrator, Disintegrating Type Specification Sheet; Prednisone Tablets RS, Lot O0C056, USP, Rockville, MD, Official December 6, 2004
4. A Comparison of Dissolution Results Using O-ring vs. Clipped Basket Shafts; Vivian Gray, Mary Beggy, Robert Brockson, Nancy Corrigan and John Mullen, Dissolution Technologies, 2001, 8 (4), 8-11.
5. Dissolution Calibration: Recommendations for Reduced Chemical Testing and Enhanced Mechanical Calibration; Pharmacopeial Forum, 26 (4), 1149-1166.