A Population Growth Model of Dissolution

[1]  L. Kier,et al.  A Cellular Automata Model of Dissolution , 1995, Pharmaceutical Research.

[2]  J. Crison,et al.  A Theoretical Basis for a Biopharmaceutic Drug Classification: The Correlation of in Vitro Drug Product Dissolution and in Vivo Bioavailability , 1995, Pharmaceutical Research.

[3]  Gordon L. Amidon,et al.  Estimating the Fraction Dose Absorbed from Suspensions of Poorly Soluble Compounds in Humans: A Mathematical Model , 1993, Pharmaceutical Research.

[4]  G L Amidon,et al.  Novel approach to the analysis of in vitro-in vivo relationships. , 1996, Journal of pharmaceutical sciences.

[5]  G L Amidon,et al.  Transport approaches to the biopharmaceutical design of oral drug delivery systems: prediction of intestinal absorption. , 1996, Advanced drug delivery reviews.

[6]  Umesh V. Banakar,et al.  Pharmaceutical Dissolution Testing , 1991 .

[7]  H. Abdou Dissolution, Bioavailability and Bioequivalence , 1990 .

[8]  S. Wiggins Introduction to Applied Nonlinear Dynamical Systems and Chaos , 1989 .

[9]  S. Davis,et al.  Alimentary tract andpancreas Transit ofpharmaceutical dosage forms through the , 1986 .

[10]  Robert M. May,et al.  Simple mathematical models with very complicated dynamics , 1976, Nature.

[11]  R. H. Leach,et al.  Dissolution and bioavailability of digoxin tablets , 1973, The Journal of pharmacy and pharmacology.

[12]  H. Davenport Physiology of the digestive tract : an introductory text , 1971 .

[13]  G. Levy EFFECT OF CERTAIN TABLET FORMULATION FACTORS ON DISSOLUTION RATE OF THE ACTIVE INGREDIENT. I. IMPORTANCE OF USING APPROPRIATE AGITATION INTENSITIES FOR IN VITRO DISSOLUTION RATE MEASUREMENTS TO REFLECT IN VIVO CONDITIONS. , 1963, Journal of pharmaceutical sciences.

[14]  A. Noyes,et al.  The rate of solution of solid substances in their own solutions , 1897 .