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Richard Wilker Korsmeyer

Other affiliations: Purdue University
Bio: Richard Wilker Korsmeyer is an academic researcher from Pfizer. The author has contributed to research in topics: Controlled release & Dosage form. The author has an hindex of 18, co-authored 29 publications receiving 6494 citations. Previous affiliations of Richard Wilker Korsmeyer include Purdue University.

Papers
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Journal ArticleDOI
TL;DR: In this article, the role of dynamic swelling and the dissolution of the polymer matrix on the release mechanism was discussed, as well as the effect of the tracer/excipient ratio on the poly(vinyl alcohol) release profile.

4,397 citations

Journal ArticleDOI
TL;DR: In this article, drug release mechanisms from, and diffusion processes in hydrophilic crosslinked polymeric systems were investigated in two macromolecular states: in the glassy and rubbery states during the early part of countercurrent water diffusion, and in the rubbery state after thermodynamic equilibrium between the network and the surrounding dissolution medium (water) was attained.

399 citations

Journal ArticleDOI
TL;DR: The release of potassium chloride from hydroxypropyl methylcellulose matrices was investigated for tablets prepared with several different compression forces and it was determined that the release kinetics for these systems deviates significantly from the classical t1/2 dependence.

322 citations

Journal ArticleDOI
TL;DR: In this article, a mathematical model for describing diffusion of a penetrant and a solute in a swellable polymer slab was applied to the case of a hydrophilic polymer loaded with a soluble drug in which the penetrant (water) is sorbed and solute (drug) is desorbed.
Abstract: A mathematical model developed to describe diffusion of a penetrant and a solute in a swellable polymer slab was applied to the case of a hydrophilic polymer loaded with a soluble drug in which the penetrant (water) is sorbed and solute (drug) is desorbed. An exponential dependence of the penetrant and solute diffusion coefficients on penetrant concentration was chosen and shown to be adequate for description of the systems studied. Experimental verification of the model was conducted by using copolymers of 2-hydroxyethyl methacrylate (HEMA) and N-vinyl-2-pyrrolidone (NVP). The monomers were bulk polymerized with benzoyl peroxide initiator and cut into thin disks. Monomer mole fractions of HEMA in the copolymers were 0.707, 0.446, and 0.211. Swelling behavior of the samples was observed in water at 37 and 0°C. Solute-containing samples were prepared and solute release from these samples into water was followed by monitoring the UV absorption of the release medium. The concentration dependence of the diffusivity of water and two model solutes, sodium trifluoroacetate and sodium heptafluorobutyrate, in the gels was studied by using the pulsed-gradient spin-echo NMR technique. The diffusivities measured by this technique followed the concentration dependence predicted by the free-volume theory. The simple exponential dependence used in the model was an adequate approximation of this behavior in the case of a transient diffusion experiment.

249 citations

Journal ArticleDOI
TL;DR: In this article, a mathematical model was developed to describe diffusion of a penetrant and a solute in a swellable polymer slab, in which the penetrant (water) is sorbed and solute is desorbed.
Abstract: A mathematical model was developed to describe diffusion of a penetrant and a solute in a swellable polymer slab. The model was applied to the case of a hydrophilic polymer loaded with a soluble bioactive agent, in which the penetrant (water) is sorbed and solute is desorbed. The model allows the incorporation of any appropriate form of the diffusion coefficients. A Fujita-type exponential dependence on penetrant concentration was chosen and shown to be adequate for prediction of a range of transport behavior. Dimensional changes in the sample were predicted by allowing each spatial increment to expand according to the amount of penetrant sorbed. During the initial period of release, the swelling was restricted to one dimension by the glassy core of the sample. At a later point in the process, the center of the sample had sorbed enough penetrant to plasticize it, and the sample relaxed to an isotropically swollen state; thereafter swelling was three-dimensional.

240 citations


Cited by
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Journal ArticleDOI
TL;DR: Drug dissolution from solid dosage forms has been described by kinetic models in which the dissolved amount of drug (Q) is a function of the test time, t or Q=f(t).

4,794 citations

Journal ArticleDOI
TL;DR: In this article, the role of dynamic swelling and the dissolution of the polymer matrix on the release mechanism was discussed, as well as the effect of the tracer/excipient ratio on the poly(vinyl alcohol) release profile.

4,397 citations

Journal ArticleDOI
TL;DR: In this paper, an exponential relation M t /M ∞ = kt n may be used to describe the Fickian and non-Fickian release behavior of release systems which are prepared by incorporation of a drug in a hydrophilic, initially glassy polymer.

3,522 citations

Journal ArticleDOI
TL;DR: The aim of this article is to present a concise review on the applications of hydrogels in the pharmaceutical field, hydrogel characterization and analysis of drug release from such devices.

3,484 citations

Journal ArticleDOI
TL;DR: The present article is a comprehensive review of the current state of the art of mathematical modeling drug release from HPMC-based delivery systems and discusses the crucial points of the most important theories.

2,354 citations