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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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Preparation and Evaluation of Novel pH‐Sensitive Poly(butyl acrylate‐co‐itaconic acid) Hydrogel Microspheres for Controlled Drug Delivery

TL;DR: In this article, a series of pH-sensitive copolymeric butyl acrylate-co-itaconic acid (p(BA-co)-IA) hydrogel microspheres were prepared by modified suspension polymerization of polyethylene glycol dimethacrylate as a crosslinker and 1% benzoyl peroxide as an initiator.
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Properties of solvent-cast chitin membranes and exploration of potential applications

TL;DR: It is suggested that the chitin membranes are promising candidates for application in next-generation wound treatment systems and support the concept of using wound dressing materials for tissue engineering and drug delivery purposes, especially for patients suffering from chronic wounds.
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Quantitative structure-transportability relationship for the release of a series of substituted pyridines from a planar polydimethylsiloxane matrix

TL;DR: In this paper, the release of 52 compounds into water, loaded at their solubility limits in a filler-supported polydimethylsiloxane matrix, was studied using a quantitative structure-activity relationship (QSAR) approach.
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Moving boundary problem for diffusion release of drug from a cylinder polymeric matrix

TL;DR: In this article, an approximate analytical solution of moving boundary problem for diffusion release of drug from a cylinder polymeric matrix was obtained by use of refined integral method and the release kinetics has been analyzed for non-erodible matrices with perfect sink condition.

Study of Additive Effect on Mechanical Properties, Drug Release Behaviour and Mechanisms in a Monolithic System

TL;DR: In this article, the authors evaluated the effect of drug diffusion in one and two-layer systems including one layer with dispersed phases and two phases with dispersed phase phases, and classified the controlled release dosage forms based on their release mechanism.
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