REFERENCES
- Dressman J.B. Future Direction for Academic Research in Dissolution Testing. Dissolution Technol. 1999; 6(3)9
- , Dissolution Testing of Immediate Release Solid Oral Dosage Forms. US Department of Health and Human Services/Food and Drug Administration/Center for Drug Evaluation and Research, August 1997.
- Pothisiri P., Carstensen J.T. Nonsink Dissolution Rate Equation. J. Pharm. Sci. 1973; 62(9)1468–1470
- Rubinstein A., Gonen A., Friedman M. Computerized Model for Evaluating the Kinetics of In Vitro Release of Valpromide from Controlled-Release Tablets Under Nonsink Conditions. J. Pharm. Sci. 1986; 75(10)959–961
- Shah P.V., Noory A., Noory C., McCullough B., Clarke S., Everett R., Naviasky H., Srinivasan B.N., Fortman D., Skelly J.P. In Vitro Dissolution of Sparingly Water-Soluble Drug Dosage Forms. Int. J. Pharm. 1995; 125: 99–106
- Fell J.T., Mohammad H.A.H. The Wetting of Powders by Bile Salt Solutions and Gastric Juice. Int. J. Pharm. 1995; 125: 327–330
- Sjokvist E., Nystrom C., Alden M., Caram-Lelham N. Physicochemical Aspects of Drug Release. XIV. The Effects of Some Ionic and Non-Ionic Surfactants on Properties of a Sparingly Soluble Drug in Solid Dispersions. Int. J. Pharm. 1992; 79: 123–133
- Singh P., Desai S.J., Flanagan D.R., Simonelli A.P., Higuchi W.I. Mechanistic Study of the Influence of Micelle Solubilization and Hydrodynamic Factors on the Dissolution Rate of Solid Drugs. J. Pharm. Sci. 1968; 57(6)959–965
- Wade A., Weller P. J. Handbook of Pharmaceutical Excipients. 2nd Ed, The Pharmaceutical Press, London 1994; 448
- Abdou H.M. Dissolution, Bioavailability and Bioequivalence. Mack Publishing Company, Easton, PA 1989; 22