Mathematical evaluation of in vitro release profiles of hydroxypropylmethylcellulose matrix tablets containing carbamazepine associated to β-cyclodextrin
Food and Drug Administration. Center for Drug Evaluation and Research (CDER), Guidance for Industry: Dissolution Testing of Immediate Release Solid Oral Dosage Forms. Rockville. 1997;. Available in http://www.fda.gov/cder/ guidance.htm
An evaluation of fit factors and dissolution efficiency for the comparison of in vitro dissolution profiles
Anderson N.H., Bauer M., Boussac N., Khan-Malek R., Munden P., Sardaro M. An evaluation of fit factors and dissolution efficiency for the comparison of in vitro dissolution profiles. J. Pharm. Biomed. Anal. 17:1998;811-822
Comparison of in vitro dissolution profiles by ANOVA-based, model-dependent and -independent methods
Yuksel N., Kanik A.E., Baykara T. Comparison of in vitro dissolution profiles by ANOVA-based, model-dependent and -independent methods. Int. J. Pharm. 209:2000;57-67
Interpretation of percent dissolved-time plots derived from in vitro testing of conventional tablets and capsules
Wagner J.G. Interpretation of percent dissolved-time plots derived from in vitro testing of conventional tablets and capsules. J. Pharm. Sci. 58:1969;1253-1257
Investigation of factors influencing release of solid drug dispersed in inert matrices II
Desai S.J., Singh P., Simonelli A.P., Higuchi W.I. Investigation of factors influencing release of solid drug dispersed in inert matrices II. J. Pharm. Sci. 55:1966;1224-1229