Literature DB >> 11496946

Modeling heterogeneity of properties and random effects in drug dissolution.

P Lánský1, M Weiss.   

Abstract

PURPOSE: To investigate new models characterizing dissolution data obtained for heterogenous materials (model I) and under randomly time-varying conditions (model II).
METHODS: In model I, the heterogeneity of the dissolving substance introduces variation of the fractional dissolution rate. In model II, the fractional dissolution rate evolves randomly, and thus the dissolution has the characteristics of a stochastic process. This situation is studied for the constant and time-dependent means of the dissolution rate.
RESULTS: The time dynamics of the dissolved fraction is presented for model I. The standard characteristics of dissolution are derived under general conditions and for several examples. One of them is in accordance with a function found empirically (1). A duality between the time-dependency of the fractional dissolution rate and the heterogeneity of the substance is investigated. The mean and variance of the dissolved fraction are calculated for model II. A method for estimating the mean dissolution rate is proposed and illustrated using Monte-Carlo experiments.
CONCLUSIONS: It follows from model I that the heterogeneity, with the same mean properties, slows down the dissolution with respect to the homogeneous case. The second approach permits predictions about the role of the stochastic fluctuations of the dissolution rate and to establish the boundaries for the dissolution profiles.

Mesh:

Substances:

Year:  2001        PMID: 11496946     DOI: 10.1023/a:1010917118001

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


  12 in total

1.  Does the dose-solubility ratio affect the mean dissolution time of drugs?

Authors:  P Lánský; M Weiss
Journal:  Pharm Res       Date:  1999-09       Impact factor: 4.200

2.  A new approach to modelling the relationship between in vitro and in vivo drug dissolution/absorption.

Authors:  A Dunne; T O'Hara; J Devane
Journal:  Stat Med       Date:  1999-07-30       Impact factor: 2.373

3.  General solution for diffusion-controlled dissolution of spherical particles. 1. Theory.

Authors:  J Wang; D R Flanagan
Journal:  J Pharm Sci       Date:  1999-07       Impact factor: 3.534

4.  Modeling of supersaturated dissolution data.

Authors:  G Valsami; A Dokoumetzidis; P Macheras
Journal:  Int J Pharm       Date:  1999-04-30       Impact factor: 5.875

5.  A population growth model of dissolution.

Authors:  A Dokoumetzidis; P Macheras
Journal:  Pharm Res       Date:  1997-09       Impact factor: 4.200

6.  On the variability of dissolution data.

Authors:  Z Elkoshi
Journal:  Pharm Res       Date:  1997-10       Impact factor: 4.200

7.  Cycle-time and residence-time density approximations in a stochastic model for circulatory transport.

Authors:  C E Smith; P Lánský; T H Lung
Journal:  Bull Math Biol       Date:  1997-01       Impact factor: 1.758

8.  On the simulation of biological diffusion processes.

Authors:  H C Tuckwell; P Lánský
Journal:  Comput Biol Med       Date:  1997-01       Impact factor: 4.589

9.  Variation of population release kinetics in polydisperse multiparticulate systems (microcapsules, microspheres, droplets, cells) with heterogeneity of one, two or three parameters in the population of individuals.

Authors:  M Donbrow; A Hoffman; S Benita
Journal:  J Pharm Pharmacol       Date:  1988-02       Impact factor: 3.765

10.  Kinetics of Dissolution of beta-Tricalcium Phosphate

Authors: 
Journal:  J Colloid Interface Sci       Date:  1997-06-01       Impact factor: 8.128

View more
  1 in total

Review 1.  Advanced pharmacokinetic models based on organ clearance, circulatory, and fractal concepts.

Authors:  K Sandy Pang; Michael Weiss; Panos Macheras
Journal:  AAPS J       Date:  2007-06-29       Impact factor: 4.009

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.