Literature DB >> 8234168

Dissolution modeling: factors affecting the dissolution rates of polydisperse powders.

A T Lu1, M E Frisella, K C Johnson.   

Abstract

The dissolution rates of two lots of hydrocortisone (fine and coarse) were simulated using a computer program based on a Noyes-Whitney-type equation. Derivations of the equation were made to compare the accuracy of simulations using spherical and cylindrical particle geometry, with and without a time-dependent diffusion layer thickness. To approximate better the shape of the hydrocortisone particles, a shape factor was used to relate cylindrical length to radius. The most accurate simulations were obtained by assuming cylindrical geometry with and without a time-dependent diffusion layer thickness for the fine and coarse hydrocortisone, respectively. The program was also modified to simulate initial particle size distributions based on the log normal probability density function.

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Year:  1993        PMID: 8234168     DOI: 10.1023/a:1018917729477

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  5 in total

1.  Dissolution rates of finely divided drug powders. I. Effect of a distribution of particle sizes in a diffusion-controlled process.

Authors:  W I HIGUCHI; E N HIESTAND
Journal:  J Pharm Sci       Date:  1963-01       Impact factor: 3.534

2.  Model systems for dissolution of finely divided (multisized) drug powders.

Authors:  J Mauger; S Howard
Journal:  J Pharm Sci       Date:  1976-07       Impact factor: 3.534

3.  Dissolution profile of log-normal powders: exact expression.

Authors:  D Brooke
Journal:  J Pharm Sci       Date:  1973-05       Impact factor: 3.534

4.  Dissolution rate patterns of log-normally distributed powders.

Authors:  J T Carstensen; M N Musa
Journal:  J Pharm Sci       Date:  1972-02       Impact factor: 3.534

5.  Mixing-tank model for predicting dissolution rate control or oral absorption.

Authors:  J B Dressman; D Fleisher
Journal:  J Pharm Sci       Date:  1986-02       Impact factor: 3.534

  5 in total
  30 in total

1.  Exploring Canine-Human Differences in Product Performance. Part II: Use of Modeling and Simulation to Explore the Impact of Formulation on Ciprofloxacin In Vivo Absorption and Dissolution in Dogs.

Authors:  M N Martinez; B Mistry; V Lukacova; K A Lentz; J E Polli; S W Hoag; T Dowling; R Kona; R M Fahmy
Journal:  AAPS J       Date:  2017-03-06       Impact factor: 4.009

2.  A modified approach to predict dissolution and absorption of polydisperse powders.

Authors:  John C Butcher; Sanjay Garg; Dawoomi Kim; Puneet Sharma
Journal:  Pharm Res       Date:  2008-06-04       Impact factor: 4.200

Review 3.  Understanding the effect of API properties on bioavailability through absorption modeling.

Authors:  Filippos Kesisoglou; Yunhui Wu
Journal:  AAPS J       Date:  2008-11-06       Impact factor: 4.009

4.  In vitro-in vivo correlation of efavirenz tablets using GastroPlus®.

Authors:  Thiago da Silva Honório; Eduardo Costa Pinto; Helvécio Vinicius A Rocha; Valeria Sant'Anna Dantas Esteves; Tereza Cristina dos Santos; Helena Carla Rangel Castro; Carlos Rangel Rodrigues; Valeria Pereira de Sousa; Lucio Mendes Cabral
Journal:  AAPS PharmSciTech       Date:  2013-08-14       Impact factor: 3.246

5.  Powder dissolution method for estimating rotating disk intrinsic dissolution rates of low solubility drugs.

Authors:  Konstantin Tsinman; Alex Avdeef; Oksana Tsinman; Dmytro Voloboy
Journal:  Pharm Res       Date:  2009-06-19       Impact factor: 4.200

6.  Effect of change in shape factor of a single crystal on its dissolution behavior.

Authors:  M V Dali; J T Carstensen
Journal:  Pharm Res       Date:  1996-01       Impact factor: 4.200

7.  Guidance in the setting of drug particle size specifications to minimize variability in absorption.

Authors:  K C Johnson; A C Swindell
Journal:  Pharm Res       Date:  1996-12       Impact factor: 4.200

8.  A Novel Approach for Analyzing the Dissolution Mechanism of Solid Dispersions.

Authors:  Yuanhui Ji; Raphael Paus; Anke Prudic; Christian Lübbert; Gabriele Sadowski
Journal:  Pharm Res       Date:  2015-02-27       Impact factor: 4.200

9.  In silico prediction of drug dissolution and absorption with variation in intestinal pH for BCS class II weak acid drugs: ibuprofen and ketoprofen.

Authors:  Yasuhiro Tsume; Peter Langguth; Alfredo Garcia-Arieta; Gordon L Amidon
Journal:  Biopharm Drug Dispos       Date:  2012-08-21       Impact factor: 1.627

10.  Application of physiologically based absorption modeling to formulation development of a low solubility, low permeability weak base: mechanistic investigation of food effect.

Authors:  Hefei Zhang; Binfeng Xia; Jennifer Sheng; Tycho Heimbach; Tsu-Han Lin; Handan He; Yanfeng Wang; Steven Novick; Ann Comfort
Journal:  AAPS PharmSciTech       Date:  2014-01-17       Impact factor: 3.246

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