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Release of medroxyprogesterone acetate from a silicone polymer.

T. J. Roseman, +1 more
- 01 Mar 1970 - 
- Vol. 59, Iss: 3
TLDR
In this paper, the physicochemical factors involved in the in vitro release of medroxyprogesterone acetate (MPA) a water-insoluble steroid embedded in a silicone rubber matrix was based upon a model system which considered the matric boundary diffusion layer.
Abstract
A study of the physicochemical factors involved in the in vitro release of medroxyprogesterone acetate (MPA) a water-insoluble steroid embedded in a silicone rubber matrix was based upon a model system which considered the matric boundary diffusion layer; extensive mathematical equations for the model are presented for planar and cylindrical cases. Initial and long-time release rates were obtained. Zones of MPA depletion were measured microscopically as a function of time and the partition coefficient of MPA was determined. Following relatively constant initial release rates a nonlinear dependence of release rates upon MPA concentration (3% 12% 24%) was found. As MPA diffused from the matrix well-defined zones of depletion developed and were photographed. Comparison of the present model to the T. Higuchi model of drug release (based on a purely matrix-controlled system) indicated that when boundary layer was considered a better fit of experimental data to theory was found. Findings suggest that the partition coefficient diffusion coefficients medroxyprogesterone acetate concentration within the polymer and agitation conditions play important roles in the release process. The applicability of the model to an in vivo system (in which slower release of MPA has been observed) is evaluated.

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References
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Journal ArticleDOI

Once Daily Sustained-Release Matrix Tablet of Naproxen: Formulation and In Vitro Evaluation

TL;DR: The results of dissolution studies indicated that higher polymer content in the matrix decreased the release rate of the drug as shown in formulation NMK4MF6 and NMK15MF6, the most successful formulations of the study, exhibited satisfactory drug release which was very close to the theoretical release profile.
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Diffusional release of a dispersed solute from a cylindrical polymeric matrix into an infinite external volume

TL;DR: Comparisons have been made between numerical and analytical exact solutions in upper and lower bounds and the presented results validate the proposed numerical solution.
Journal ArticleDOI

Methods of following drug release from controlled release dosage forms

TL;DR: The design conditions for in vitro release systems are outlined, and factors such as drug solubility, solution diffusivitiy and hydrodynamics, as well as in vitro-in vivo correlations are discussed.
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Mechanistical Analysis of Release Kinetics for Lipophilic Drug from Matrix-Type Drug Delivery Devices

TL;DR: The results reveal that intrinsic release, calculated from the model, shows the true properties of the drug delivery system, which might have been disguised by the boundary layer effect.
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Diffusive desorption of small solute molecules from amorphous polymers: poly(methyl methacrylate), poly (vinyl acetate) and poly(n-alkyl 2-cyanoacrylates)

TL;DR: In this paper, the diffusion coefficient of poly(vinyl acetate) and poly(methyl methacrylate) was measured from desorption rates into aqueous buffers from solid solutions of diffusant in cast polymer films.
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