Development of diclofenac sodium controlled release solid dispersion tablet using optimization strategy

Drug Development and Industrial Pharmacy

Volumn 23, Issue 8, 1997, Pages 843-848

  Dangprasirt, P ^a   Ritthidej, G C ^b  

^a RANGSIT UNIVERSITY   (Thailand)

^b CHULALONGKORN UNIVERSITY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

AEROSIL; CHITOSAN; CROSCARMELLOSE SODIUM; DICLOFENAC; ERA TAB; ETHYL CELLULOSE; EXCIPIENT; MAGNESIUM STEARATE; SILICON DIOXIDE; STARCH; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED RELEASE FORMULATION; CONTROLLED STUDY; DIFFUSION; DISPERSION; DISSOLUTION; DRUG RELEASE; MULTIPLE REGRESSION; PHYSICAL PARAMETERS; SOLID; TABLET; TABLET COMPRESSION; TECHNIQUE;

EID: 0030795918     PISSN: 03639045     EISSN: None     Source Type: Journal    
DOI: 10.3109/03639049709150556     Document Type: Article

References (8)

1. P. Dangprasirt and G. C. Ritthidej, Drug Dev. Ind. Pharm., 21, 2323 (1995).
2. H. A, Abdou, Dissolution, Bioavailability & Bioequivalence, Mack Printing Company, Easton, Pennsylvania, 1989.
3. T. Iranloye and E. Parrott, J. Pharm. Sci., 67, 535 (1978).
4. H. Smith, C. Baker, and J. Wood, J. Pharm. Pharmacol., 23, 536 (1971).
5. S. Solvang and P. Finholt, J. Pharm. Sci., 59, 49 (1970).
6. S. Viravinit and A. Mitrivej, in Microbial Utilization of Renewable Resources, Vol. 6, International Center of Cooperative Research in Biotechnology, Osaka, 1989, p. 158.
7. D. C. Montgomery, Design and Analysis of Experiments, 3rd ed., John Wiley & Sons Inc., New York, 1991.
8. The United States Pharmacopeia, 22th rev., The National Formulary, 17th ed., The United States Pharmacopeil Convention Inc., Rockville, 1990.