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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

Characterization of Solid Dispersion Phase Transitions Using a New Optical Thermal Analyzer

TL;DR: In this paper, the phase transitions occurring during the heating of progesterone PEG6000, and the solid dispersions (3% and 20% w/w) were studied using differential scanning calorimetry and optical thermal analysis.
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In Vivo Performance of Wax Matrix Granules Prepared by a Twin-Screw Compounding Extruder

TL;DR: Good correlation between one in vitro dissolution parameter (mean dissolution time, MDT) and two in vivo parameters (AUC12 and MRT) suggested that it would be possible to design WMGs with a desired in vivo performance by controlling HPC content.
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A study of enteric-coated liquid-filled hard gelatin capsules with biphasic release characteristics

TL;DR: The present investigation demonstrates the importance of ensuring a sufficient enteric-coating level for oral dosage vehicles to maintain post gastric dissolution characteristics and illustrates the need for a reliable means of assessing enteric coat performance in vitro.
Journal ArticleDOI

Characterization of Hydrogen Bonding between Selected Barbiturates and Polyethylene Glycol 4000 by IR Spectral Analysis

TL;DR: Several barbiturates and primidone were equilibrated with polyethylene glycol 4000 in pyridine and IR spectral properties of these samples indicate that seven disubstituted bar Biturates complex withpolyethylene Glycol 4000 while five disubStitutedbarbiturate and two trisubst ituted bar biturates as well as primid one do not.
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Influence of a lipophilic thermal lubricant on the processing conditions and drug release properties of chlorpheniramine maleate tablets prepared by hot-melt extrusion

TL;DR: In this article, the influence of a lipophilic thermal lubricant on the processing conditions and properties of chlorpheniramine maleate (CPM) tablets prepared by hot-melt extrusion was investigated.
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