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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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Modeling of dispersed-drug release from two-dimensional matrix tablets.

TL;DR: A mathematical model was developed and analytical solutions were obtained for dispersed-drug release from two-dimensional matrix tablets in a perfect sink to describe kinetics of solute release from matrices with isotropic or anisotropic properties.
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Mechanisms of Isoniazid Release from Poly(d,I-lactide-co-glycolide) Matrices Prepared by Dry-Mixing and Low Density Polymeric Foam Methods

TL;DR: The release mechanisms of a small molecular drug from biodegradable poly(d,l-lactide-co-glycolide) cylindrical matrices were investigated and Isoniazid (INH), one of the most effective drugs against tuberculosis (TB), was selected as the model drug.
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Transport studies on macromolecules used as drug carriers

TL;DR: A review of the transport of drug molecules through physiological systems via polymeric materials can be found in this paper, where a brief introduction to the fundamentals and concepts which are frequently used in the drug-delivery area are covered in the following sections.
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Poly(ε-caprolactone) and Eudragit® microparticles containing fludrocortisone acetate

TL;DR: In this paper, the authors compared different formulations of fludrocortisone microparticles for the treatment of mineralocorticoid insufficiency and found that the use of a suspension of micronized drug in dichloromethane as dispersed phase significantly improved the process.
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Synthesis and characterization of novel poly(sebacic anhydride-co-Pluronic F68/F127) biopolymeric microspheres for the controlled release of nifedipine

TL;DR: In vitro release studies of NFD from poly(sebacic anhydride-co-Pluronic-F68/F127) microspheres performed in pH 7.4 phosphate buffer indicated sustained release rates of N FD at higher amounts of Pluronic in polyanhydride copolymers.
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