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Journal ArticleDOI

Evaluation of hot-melt extrusion as a new technique for the production of polymer-based pellets for sustained release capsules containing high loadings of freely soluble drugs

TLDR
In this paper, hot-melt screw extrusion was presented as an alternative method for producing polymer-based sustained release (SFL) pellets, which were produced with diltiazem hydrochloride as model drug.
Abstract
Hot-melt screw extrusion was presented as an alternative method for producing polymer-based sustained release pellets. Special care was paid to the case of highly dosed freely soluble drugs which often pose technological problems with the usual manufacturing processes. In a preformulation study, polymers, plasticizers and drugs were selected according to various criteria including thermal stability. During these preliminary tests, the optimum extrusion conditions were defined. Four polymers were considered for extrusion trials, namely ethylcellulose, cellulose acetate butyrate, poly(ethylene-co-vinyl acetate) and a polymethacrylate derivative (Eudragit® RSPM). Pellets were produced with diltiazem hydrochloride as model drug. The surface appearance of various formulations was examined and the porosity assessed by means of mercury porosimetry. A distinct structure was found for the EVAC-based pellets. The overall porosity was less than 10%. Lastly, in vitro release of the drug showed a biphasic prof...

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Citations
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Journal ArticleDOI

Melt extrusion: from process to drug delivery technology

TL;DR: Improved bioavailability was achieved again demonstrating the value of the technology as a drug delivery tool, with particular advantages over solvent processes like co-precipitation.
Journal ArticleDOI

Pharmaceutical Applications of Hot-Melt Extrusion: Part I

TL;DR: The pharmaceutical applications of hot-melt extrusion, including equipment, principles of operation, and process technology, are reviewed and the physicochemical properties of the resultant dosage forms are described.
Journal ArticleDOI

Hot-Melt Extrusion: from Theory to Application in Pharmaceutical Formulation

TL;DR: This review discussed the importance of using the quality by design approach in drug development, evaluated the process analytical technology used in pharmaceutical HME monitoring and control, discussed techniques used in HME, and emphasized the potential for monitoring and controlling hot-melt technology.
Journal ArticleDOI

Eudragit®: a technology evaluation

TL;DR: In this review, the physicochemical characteristics and applications of different grades of Eudragit in colon-specific/enteric-coated/sustained release drug delivery and taste masking have been addressed.
Journal ArticleDOI

Use of surfactants as plasticizers in preparing solid dispersions of poorly soluble API: selection of polymer-surfactant combinations using solubility parameters and testing the processability.

TL;DR: Thermal analysis of the API-polymer-surfactant blends suggested that the surfactants caused solvation/plasticization, manifesting in reduction of the melting of API and T(m) of polymers and the combined T(g) of the solid dispersion formed from quench cooling.
References
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Journal ArticleDOI

Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matrices

TL;DR: The analyses suggest that for the latter system the time required to release 50% of the drug would normally be expected to be approximately 10 per cent of that required to dissolve the last trace of the solid drug phase in the center of the pellet.

Biopharmaceutical comparison of oral multiple-unit and single-unit sustained-release dosage forms

N. Follonier, +1 more
TL;DR: In this article, auteurs passent en revue les travaux portant sur la comparaison des formes a liberation prolongee divisees and monolithiques destinees a la voie orale.
Journal ArticleDOI

Physical and Chemical Factors Influencing the Release of Drugs from Acrylic Resin Films

TL;DR: The rate of drug release increased with increasing temperature and adsorption of salicylic acid by the polymers was believed to influence the drug release profiles observed for different drug loadings and ionic strengths.
Journal ArticleDOI

Regulation of Dissolution Rate by Pellet Geometry

TL;DR: The study was undertaken to determine the in vitro sustained release characteristics of pellets of a form such that their loss of effective surface area during dissolution is minimized.
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