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Journal ArticleDOI

Pharmaceutical Applications of Hot-Melt Extrusion: Part I

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TLDR
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.
Abstract
Interest in hot-melt extrusion techniques for pharmaceutical applications is growing rapidly with well over 100 papers published in the pharmaceutical scientific literature in the last 12 years. Hot-melt extrusion (HME) has been a widely applied technique in the plastics industry and has been demonstrated recently to be a viable method to prepare several types of dosage forms and drug delivery systems. Hot-melt extruded dosage forms are complex mixtures of active medicaments, functional excipients, and processing aids. HME also offers several advantages over traditional pharmaceutical processing techniques including the absence of solvents, few processing steps, continuous operation, and the possibility of the formation of solid dispersions and improved bioavailability. This article, Part I, reviews the pharmaceutical applications of hot-melt extrusion, including equipment, principles of operation, and process technology. The raw materials processed using this technique are also detailed and the physicochemical properties of the resultant dosage forms are described. Part II of this review will focus on various applications of HME in drug delivery such as granules, pellets, immediate and modified release tablets, transmucosal and transdermal systems, and implants.

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Citations
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Journal ArticleDOI

Strategies to Address Low Drug Solubility in Discovery and Development

TL;DR: The article provides an integrated and contemporary discussion of current approaches to solubility and dissolution enhancement but has been deliberately structured as a series of stand-alone sections to allow also directed access to a specific technology where required.
Journal ArticleDOI

Current trends and future perspectives of solid dispersions containing poorly water-soluble drugs.

TL;DR: Critical aspects and recent advances in formulation, preparation and characterization of solid dispersions as well as in-depth pharmaceutical solutions to overcome some problems and issues that limit the development and marketability of solid dispersion products are reviewed.
Journal ArticleDOI

Effect of geometry on drug release from 3D printed tablets.

TL;DR: This work has demonstrated the potential of 3DP to manufacture tablet shapes of different geometries, many of which would be challenging to manufacture by powder compaction.
Journal ArticleDOI

Manufacture and characterization of mucoadhesive buccal films.

TL;DR: This review will consider the literature that describes the manufacture and characterization of mucoadhesive buccal films and hot-melt extrusion has been explored as an alternative manufacturing process and has yielded promising results.
Journal ArticleDOI

3D Printing of Medicines: Engineering Novel Oral Devices with Unique Design and Drug Release Characteristics

TL;DR: The study confirms the potential of 3D printing to fabricate multiple-drug containing devices with specialized design configurations and unique drug release characteristics, which would not otherwise be possible using conventional manufacturing methods.
References
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Journal ArticleDOI

Matrix pellets based on the combination of waxes, starches and maltodextrins

TL;DR: In this paper, the authors used microcrystalline waxes, pregelatinized starches and hydrolysed starches to produce matrix pellets, which were used as model drugs.
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Properties of Tablets Containing Granulations of Ibuprofen and an Acrylic Copolymer Prepared by Thermal Processes

TL;DR: HME was shown to be a novel method to prepare matrix tablets and stable dissolution properties were obtained when tablets were stored at 40°C for 30 days.
Journal ArticleDOI

Effect of supersaturation and crystallization phenomena on the release properties of a controlled release device based on EVA copolymer

TL;DR: It was found that if the amount of etonogestrel is below a critical nucleation concentration at room temperature, the dissolved steroid remains in a supersaturated state, and if on the other hand theamount of dissolved steroid is just above the criticalucleation concentration, the supersaturated steroid recrystallizes very slowly.
Journal ArticleDOI

Production of enteric capsules by means of hot-melt extrusion.

TL;DR: It can be concluded that hot-melt extruded capsules seem suitable as an alternative for enteric coating because of their suitability for ileal or colonic drug targeting.
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