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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

Release of hydrocortisone from a cream matrix: dependency of release on suspension concentration and measurement of solubility and diffusivity.

TL;DR: The overall behavior fit theoretical expectations for suspensions having only a small fraction of the drug they contain in solution, and the square root of time release rate from run to run was directly proportional to thesquare root of the total concentration of hydrocortisone placed in the formulations.
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The release mechanism of drags from polyurethane transdermal delivery systems

TL;DR: In this paper, a boundary solvent layer formed at the device-skin interface may provide zero-order release patterns for transdermal delivery systems, devices applied to the skin in non-stirred environments and designed as solvated matrices.
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Modeling of drug delivery from erodible and non-erodible laminated planar devices into a finite external medium

TL;DR: Analytical solutions based on the pseudo-steady state approximation (PSSA) were derived for the case of controlled dispersed-drug release from erodible and non-erodible planar matrices, through a membrane, and taking into account the existence of a diffusion boundary layer and a finite release medium.
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Drug-incorporated silicone discs as sustained release capsules. I. Chloroquine diphosphate.

TL;DR: Results from samples prepared from different batches of polymer showed comparable results, indicating the rather homogeneous nature of the polymer-drug system.
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