Literature DB >> 3735090

Dissolution of theophylline monohydrate and anhydrous theophylline in buffer solutions.

J H de Smidt, J G Fokkens, H Grijseels, D J Crommelin.   

Abstract

The dissolution kinetics of theophylline monohydrate and anhydrous theophylline were investigated with a rotating-disk apparatus in buffer solutions at 298 K under sink conditions. The observed dissolution rate of theophylline monohydrate under various conditions agreed well with predictions based on the Extended Simultaneous Chemical Reaction and Dissolution concept. Below 337 K, anhydrous theophylline is converted to theophylline monohydrate in contact with water. The dissolution profile of anhydrous theophylline can be divided into three phases: a pre-transformation phase: anhydrous theophylline dissolves; the transformation phase, during which its dissolution rate drops to the level of the theophylline monohydrate dissolution rate; and steady state, at which the dissolution rate of anhydrous theophylline equals the dissolution rate of theophylline monohydrate. The presence of theophylline monohydrate crystals at the dissolving surface was confirmed by IR spectroscopy and microscopic observation. The length of the transformation phase, depending on the characteristics of the diffusion boundary layer, varied with the experimental conditions (e.g., pH and rotation speed). It was concluded that during the dissolution process the disk is covered with theophylline monohydrate crystals that precipitate from the supersaturated medium adjacent to the disk surface, and that crystallization of theophylline monohydrate is a precipitation process controlled by hydrodynamic and diffusion parameters.

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Year:  1986        PMID: 3735090     DOI: 10.1002/jps.2600750515

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


  6 in total

1.  Experimental determinations of diffusion coefficients in dilute aqueous solution using the method of hydrodynamic stability.

Authors:  M Z Southard; L J Dias; K J Himmelstein; V J Stella
Journal:  Pharm Res       Date:  1991-12       Impact factor: 4.200

2.  Crystal growth kinetics of theophylline monohydrate.

Authors:  N Rodríguez-Hornedo; H J Wu
Journal:  Pharm Res       Date:  1991-05       Impact factor: 4.200

3.  A method to predict blood-brain barrier permeability of drug-like compounds using molecular dynamics simulations.

Authors:  Timothy S Carpenter; Daniel A Kirshner; Edmond Y Lau; Sergio E Wong; Jerome P Nilmeier; Felice C Lightstone
Journal:  Biophys J       Date:  2014-08-05       Impact factor: 4.033

4.  The influence of water content of triglyceride oils on the solubility of steroids.

Authors:  Laura M Land; Ping Li; Paul Michael Bummer
Journal:  Pharm Res       Date:  2005-05-17       Impact factor: 4.200

5.  Dissolution behavior of a poorly water soluble compound in the presence of Tween 80.

Authors:  Linna R Chen; James A Wesley; Shobha Bhattachar; Bienvenido Ruiz; Korey Bahash; Suresh R Babu
Journal:  Pharm Res       Date:  2003-05       Impact factor: 4.200

6.  Dissolution of an ensemble of differently shaped poly-dispersed drug particles undergoing solubility reduction: mathematical modelling.

Authors:  Michela Abrami; Lucia Grassi; Rosario di Vittorio; Dritan Hasa; Beatrice Perissutti; Dario Voinovich; Gabriele Grassi; Italo Colombo; Mario Grassi
Journal:  ADMET DMPK       Date:  2020-07-14
  6 in total

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