Literature DB >> 7816758

A convective-diffusion model for dissolution of two non-interacting drug mixtures from co-compressed slabs under laminar hydrodynamic conditions.

S Neervannan1, L S Dias, M Z Southard, V J Stella.   

Abstract

A numerical convective-diffusion dissolution model has been extended to describe dissolution of two neutral non-interacting drugs co-compressed in a slab geometry. The model predicted the experimental dissolution rates of naproxen/phenytoin mixtures and hydrocortisone/nitrofurantoin mixtures quite accurately, except for phenytoin in the naproxen/phenytoin mixture at low weight proportions. A non-linear dependence of dissolution rate on weight proportion with a positive deviation from linearity was observed. An increase in flow rate increased the dissolution rate and the cube-root dependency of dissolution rate on the flow rate for a given weight proportion of the component in the slab, as proposed earlier by Shah and Nelson for pure compounds, was also observed here, suggesting that the changes in dissolution profile were caused by changes in surface area only. As expected from the model an increase in particle size of the powders used to make the slab decreased the dissolution rate. This was explained by an increase in the average length of the component resulting in a bigger 'carryover' of material from one section of the component in the slab to the next section of the same component, due to convection, and hence lower flux.

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Year:  1994        PMID: 7816758     DOI: 10.1023/a:1018942411536

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


  10 in total

1.  Dissolution of two-component solids.

Authors:  S A Shah; E L Parrott
Journal:  J Pharm Sci       Date:  1976-12       Impact factor: 3.534

2.  Convective diffusion model for a transport-controlled dissolution rate process.

Authors:  K G Nelson; A C Shah
Journal:  J Pharm Sci       Date:  1975-04       Impact factor: 3.534

3.  Evaluation of a convective diffusion drug dissolution rate model.

Authors:  A C Shah; K G Nelson
Journal:  J Pharm Sci       Date:  1975-09       Impact factor: 3.534

4.  Dissolution of ionizable drugs into unbuffered solution: a comprehensive model for mass transport and reaction in the rotating disk geometry.

Authors:  M Z Southard; D W Green; V J Stella; K J Himmelstein
Journal:  Pharm Res       Date:  1992-01       Impact factor: 4.200

Review 5.  The gastrointestinal absorption of drugs in man: a review of current concepts and methods of investigation.

Authors:  J Hirtz
Journal:  Br J Clin Pharmacol       Date:  1985       Impact factor: 4.335

6.  General model for dissolution rates of n-component, nondisintegrating spheres.

Authors:  G R Carmichael; S A Shah; E L Parrott
Journal:  J Pharm Sci       Date:  1981-12       Impact factor: 3.534

7.  Dissolution kinetics of carboxylic acids I: effect of pH under unbuffered conditions.

Authors:  K G Mooney; M A Mintun; K J Himmelstein; V J Stella
Journal:  J Pharm Sci       Date:  1981-01       Impact factor: 3.534

8.  Dissolution rates of polyphase mixtures.

Authors:  W I Higuchi; N A Mir; S J Desai
Journal:  J Pharm Sci       Date:  1965-10       Impact factor: 3.534

9.  Dissolution of acidic and basic compounds from the rotating disk: influence of convective diffusion and reaction.

Authors:  D P McNamara; G L Amidon
Journal:  J Pharm Sci       Date:  1986-09       Impact factor: 3.534

10.  Reaction plane approach for estimating the effects of buffers on the dissolution rate of acidic drugs.

Authors:  D P McNamara; G L Amidon
Journal:  J Pharm Sci       Date:  1988-06       Impact factor: 3.534

  10 in total
  2 in total

1.  A new approach to dissolution testing by UV imaging and finite element simulations.

Authors:  Johan P Boetker; Jukka Rantanen; Thomas Rades; Anette Müllertz; Jesper Ostergaard; Henrik Jensen
Journal:  Pharm Res       Date:  2013-01-11       Impact factor: 4.200

2.  Dependence of dissolution rate on surface area: is a simple linear relationship valid for co-compressed drug mixtures?

Authors:  S Neervannan; M Z Southard; V J Stella
Journal:  Pharm Res       Date:  1994-10       Impact factor: 4.200

  2 in total

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