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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

Controlled release of insect sex pheromones from paraffin wax and emulsions.

TL;DR: Sprayable formulations can be designed to release insect pheromones to the environment at a rate necessary for insect control by mating disruption, and at temperatures below 38 degreesC, zero-order release was observed.
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Controlled Release Delivery Systems

TL;DR: The properties of release profiles provided by various designs of system are qualitatively and quantitatively described, with respect to areas of current and potential application.
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Modeling and analysis of dispersed-drug release into a finite medium from sphere ensembles with a boundary layer.

TL;DR: Criteria were established for finding the conditions when drug release would stall due to saturation of the medium, which can be used to determine suitable liquid volume and time for refreshing the medium.
Journal ArticleDOI

Evaluation, Control, and Prediction of Drug Diffusion Through Polymeric Membranes III: Diffusion of Barbiturates, Phenylalkylamines, Dextromethorphan, Progesterone, and Other Drugs

TL;DR: The apparent diffusion constants through silastic membrane were determined by steady-state studies for a series of barbiturates and phenylalkylamines and correlated with the determined chloroform/acetate buffer partition coefficients in the former case.
Journal ArticleDOI

Application of the Higuchi model for drug release from dispersed matrices to particles of general shape

TL;DR: An equation has been derived which describes the short time behaviour of the release of a dispersed drug from a homogeneous matrix of general shape using the pseudo-steady-state approximation of Higuchi and it has been used successfully to describe the experimentally observed release in vitro of Sulphamethizole.
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