Literature DB >> 11835211

General solution for diffusion-controlled dissolution of spherical particles. 2. Evaluation of experimental data.

Jianzhuo Wang1, Douglas R Flanagan.   

Abstract

Our general particle dissolution model unified three traditional particle dissolution models and predicted that dissolution rates depend on surface curvature. Spherical benzocaine particles were prepared with a hot-melt dispersion method and physicochemically characterized. Their dissolution behavior was studied to evaluate the general dissolution model. A flow-through dissolution test system was used which employed an HPLC pump, an HPLC UV detector, a cylindrical-shaped dissolution cell, and a data collection system. Single benzocaine particle dissolution profiles were determined at ambient temperature (22-23 degrees C) in water at a constant flow rate. Dissolution rate normalized by surface area was found to be particle radius-dependent and fitted well by the general particle dissolution model with a diffusion layer thickness of 110 microm and benzocaine diffusion coefficient of 1.4 x 10(-5) cm(2)/s. Analysis of literature particle dissolution data also supported this general model. Our general model accounts for literature reports of apparent diffusion layer thicknesses being smaller for small particles compared with large particles. This study supports the applicability of the general particle dissolution model for a flow-through dissolution test system. Copyright 2002 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 91:534-542, 2002

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Year:  2002        PMID: 11835211     DOI: 10.1002/jps.10039

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  10 in total

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2.  Continuous Intestinal Absorption Model Based on the Convection-Diffusion Equation.

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Review 5.  Nanotechnology: toxicologic pathology.

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Journal:  Toxicol Pathol       Date:  2013-02-06       Impact factor: 1.902

Review 6.  Population-based mechanistic prediction of oral drug absorption.

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7.  Physiologically based pharmacokinetic modeling of disposition and drug-drug interactions for valproic acid and divalproex.

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Journal:  ACS Omega       Date:  2021-12-14

9.  Quantifying the Extent of Calcification of a Coccolithophore Using a Coulter Counter.

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10.  Application of a Bayesian approach to physiological modelling of mavoglurant population pharmacokinetics.

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Journal:  J Pharmacokinet Pharmacodyn       Date:  2015-08-01       Impact factor: 2.745

  10 in total

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