Hot-Melt Extrusion Pharmaceutical Applications

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Edition: 1st
Format: Hardcover
Pub. Date: 2012-06-25
Publisher(s): Wiley
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Summary

Hot-melt extrusion (HME) - melting a substance and forcing it through an orifice under controlled conditions to form a new material - is an emerging processing technology in the pharmaceutical industry for the preparation of various dosage forms and drug delivery systems, for example granules and sustained release tablets. Hot-Melt Extrusion: Pharmaceutical Applications covers the main instrumentation, operation principles and theoretical background of HME. It then focuses on HME drug delivery systems, dosage forms and clinical studies (including pharmacokinetics and bioavailability) of HME products. Finally, the book includes some recent and novel HME applications, scale -up considerations and regulatory issues. Topics covered include: principles and die design of single screw extrusion twin screw extrusion techniques and practices in the laboratory and on production scale HME developments for the pharmaceutical industry solubility parameters for prediction of drug/polymer miscibility in HME formulations the influence of plasticizers in HME applications of polymethacrylate polymers in HME HME of ethylcellulose, hypromellose, and polyethylene oxide bioadhesion properties of polymeric films produced by HME taste masking using HME clinical studies, bioavailability and pharmacokinetics of HME products injection moulding and HME processing for pharmaceutical materials laminar dispersive & distributive mixing with dissolution and applications to HME#60;br /> technological considerations related to scale-up of HME processes devices and implant systems by HME an FDA perspective on HME product and process understanding improved process understanding and control of an HME process with near-infrared spectroscopy Hot-Melt Extrusion: Pharmaceutical Applications is an essential multidisciplinary guide to the emerging pharmaceutical uses of this processing technology for researchers in academia and industry working in drug formulation and delivery, pharmaceutical engineering and processing, and polymers and materials science.

Author Biography

Dr. Dionysios Douroumis, Senior Lecturer, School of Science, University of Greenwich, UK
After completing his postgraduate studies Dr Douroumis worked as a postdoctoral fellow at the Friedrich – Schiller University of Jena in the Department of Pharmacy, and later as a Senior Scientist at Phoqus Pharmaceutical plc, tasked with the development of sustained/pulsatile release formulations, orally disintegrating tablets and taste masking of bitter drugs; some of these studies were in collaboration with Evonik GmbH in Darmstadt, Germany. He is currently Senior Lecture at the in the University of Greenwich School of Science where he coordinates the course for the MSc Pharmaceutical Science Programme (350 students per annum) and is also a tutor for undergraduate studies in Pharmaceutical Sciences.

Table of Contents

List of Contributorsp. xv
Prefacep. xvii
Single-screw Extrusion: Principlesp. 1
Introductionp. 1
Ideal Compoundingp. 2
Basics of the Single-screw Extruderp. 3
Screw Feed Sectionp. 5
Screw Compressor Sectionp. 9
Screw Metering Sectionp. 11
Mixersp. 11
Limitations of Conventional Single-screw Mixersp. 13
SSE Elongational Mixersp. 13
Summaryp. 20
Referencesp. 21
Twin-screw Extruders for Pharmaceutical Hot-melt Extrusion: Technology, Techniques and Practicesp. 23
Introductionp. 23
Extruder Types and Working Principlep. 24
Individual Parts of a TSEp. 25
Drive Unitp. 25
Screwsp. 25
Screw Elementsp. 27
Distributive Flow Elementsp. 28
Discharge Feed Screwp. 28
Barrelp. 29
Downstreamingp. 30
Individual Processing Sections of the TSEp. 31
Feeding Sectionp. 32
Conveying/Melting Sectionp. 32
Mixing Sectionp. 33
Venting Sectionp. 33
Extrusion Sectionp. 33
Feeding of Solidsp. 34
TSE Operating Parametersp. 34
Filling Levelp. 36
Screw Speedp. 36
Feed Ratep. 37
Residence Time Distributionp. 37
Effect of Screw Speed and Feed Rate on Melt Temperaturep. 39
Setting up an HME Process using QbD Principlesp. 40
Understanding Knowledge Spacep. 40
Denning Design Spacep. 40
Determining Control Spacep. 41
Summaryp. 42
Referencesp. 42
Hot-melt Extrusion Developments in the Pharmaceutical Industryp. 43
Introductionp. 43
Advantages of HME as Drug Delivery Technologyp. 44
Formulations used for HME Applicationsp. 45
Active Pharmaceutical Ingredientp. 46
Solid Dispersionsp. 48
Bioavailability Improvementp. 49
Controlled Delivery Systemsp. 51
Plasticizersp. 53
Characterization of Extrudatesp. 55
Thermal Analysisp. 55
Atomic Force Microscopyp. 56
Residence Timep. 57
Spectroscopic Techniquesp. 57
X-ray Diffraction (XRD)p. 58
Microscopyp. 58
Drug Releasep. 58
Hot-melt Extruded Dosage Formsp. 58
Oral Drag Deliveryp. 59
Filmsp. 61
Vaginal Rings and Implantsp. 61
A View to the Futurep. 63
Referencesp. 64
Solubility Parameters for Prediction of Drug/Polymer Miscibility in Hot-melt Extruded Formulationsp. 71
Introductionp. 71
Solid Dispersionsp. 72
Basic Assumptions for the Drug-polymer Miscibility Predictionp. 77
Solubility and the Flory-Huggins Theoryp. 78
Miscibility Estimation of Drug and Monomersp. 83
Summaryp. 89
Referencesp. 90
The Influence of Plasticizers in Hot-melt Extrusionp. 93
Introductionp. 93
Traditional Plasticizersp. 94
Non-traditional Plasticizersp. 95
Specialty Plasticizersp. 104
Conclusionsp. 107
Referencesp. 108
Applications of Poly(meth)acrylate Polymers in Melt Extrusionp. 113
Introductionp. 113
Polymer Characteristicsp. 116
Chemical Structure and Molecular Weightp. 116
Glass Transition Temperaturep. 119
Plasticizersp. 120
Thermostabilityp. 121
Viscosityp. 122
Specific Heat Capacityp. 124
Hygroscopicityp. 126
Melt Extrusion of Poly(methacrylates) to Design Pharmaceutical Oral Dosage Formsp. 128
Solubility Enhancementp. 128
Bioavailability Enhancement of BCS Class IV Drugsp. 132
Controlled Releasep. 135
Time-controlled-release Dosage Formsp. 136
pH-dependent Releasep. 138
Taste Maskingp. 139
Summaryp. 140
Referencesp. 140
Hot-melt Extrusion of Ethylcellulose, Hypromellose and Polyethylene Oxidep. 145
Introductionp. 145
Backgroundp. 146
Thermal Propertiesp. 147
Processing Aids/Additivesp. 147
Unconventional Processing Aids: Drags, Blendsp. 149
Case Studiesp. 151
Ethylcellulosep. 151
Combinations of Excipientsp. 151
Solubilizationp. 155
Filmp. 159
Unique Dosage Formsp. 163
Abuse Resistancep. 163
Controlled Releasep. 164
Solubility Parametersp. 166
Milling of EC, HPMC and PEO Extrudatep. 168
Referencesp. 170
Bioadhesion Properties of Polymeric Films Produced by Hot-melt Extrusionp. 177
Introductionp. 177
Anatomy of the Oral Cavity and Modes of Drug Transportp. 180
Structurep. 180
Modes of Drug Transport and Kineticsp. 180
Factors Affecting Drug Absorptionp. 181
Mucoadhesive Mechanismsp. 182
Factors Affecting Mucoadhesion in the Oral Cavityp. 183
Determination of Mucoadhesion and Mechanical Properties of Filmsp. 183
Bioadhesive Films Prepared by HMEp. 184
Summaryp. 194
Referencesp. 194
Taste Masking Using Hot-melt Extrusionp. 201
The Need and Challenges for Masking Bitter APIsp. 201
Organization of the Taste Systemp. 203
Taste Perception in Humans and Organization of Peripheral Systemp. 203
Transduction of Taste Signalsp. 205
Taste Sensing Systems (Electronic Tongues) for Pharmaceutical Dosage Formsp. 206
Alpha MOS Electronic Tongue: Instrumentation and Operational Principlesp. 206
Taste Analysisp. 208
Taste Masking Efficiency Testingp. 209
Advantages of E-tongue Taste Analysisp. 211
Hot-melt Extrusion: An Effective Means of Taste Maskingp. 212
Taste Masking via Polymer Extrusionp. 212
Taste Masking via Solid Lipid Extrusionp. 216
Summaryp. 219
Referencesp. 219
Clinical and Preclinical Studies, Bioavailability and Pharmacokinetics of Hot-melt Extruded Productsp. 223
Introduction to Oral Absorptionp. 223
In Vivo Evaluation of Hot-melt Extruded Solid Dispersionsp. 225
Oral Immediate Releasep. 225
Oral Controlled Releasep. 232
Implantsp. 233
Conclusionp. 234
Referencesp. 234
Injection Molding and Hot-melt Extrusion Processing for Pharmaceutical Materialsp. 239
Introductionp. 239
Hot-melt Extrusion in Briefp. 240
Injection Moldingp. 241
Critical Parametersp. 242
Melt Temperaturep. 242
Barrel Temperaturep. 243
Cooling Temperaturep. 243
Holding Pressurep. 243
Holding Timep. 243
Back Pressurep. 244
Injection Speedp. 244
Cooling Time/Cycle Timep. 244
Example: Comparison of Extruded and Injection-molded Materialp. 245
Development of Products for Injection Moldingp. 246
Excipientsp. 246
Stabilityp. 248
Process Developmentp. 248
Properties of Injection-molded Materialsp. 251
EgaletĀ® Technologyp. 251
Controlling Physical State by Means of Hot-melt Extrusion and Injection Moldingp. 253
Anti-tamper Properties of Injection-molded Tabletsp. 254
Concluding Remarksp. 257
Referencesp. 257
Laminar Dispersive and Distributive Mixing with Dissolution and Applications to Hot-melt Extrusionp. 261
Introductionp. 261
Elementary Steps in HMEp. 263
Paniculate Solids Handling (PSH)p. 263
Meltingp. 263
Devolatilizationp. 264
Pumping and Pressurizationp. 265
Dispersive and Distributive Mixingp. 265
HME Processes: Cases I and IIp. 265
Case Ip. 266
Case IIp. 268
Dissolution of Drug Particulates in Polymeric Meltp. 270
Process Variablesp. 270
Equipment Variablesp. 273
Material Variablesp. 275
Case Study: Acetaminophen and Poly(ethylene oxide)p. 278
Determination of Solubility of APAP in PEOp. 280
Referencesp. 282
Technological Considerations Related to Scale-up of Hot-melt Extrusion Processesp. 285
Introductionp. 285
Scale-up Terminologyp. 287
Scale-up: Batch Sizep. 287
Scale-up: Feed Ratep. 288
Scale-up: Extruder Diameterp. 290
Volumetric Scale-upp. 290
Volumetric Scale-up: Length/Diameter (L/D)p. 292
Volumetric Scale-up: Diameter Ratiop. 292
Volumetric Scale-up: Screw Designp. 294
Power Scale-upp. 296
Heat Transfer Scale-upp. 298
Die Scale-upp. 299
Conclusionp. 299
Referencesp. 300
Devices and Implant Systems by Hot-melt Extrusionp. 301
Introductionp. 301
HME in Device Developmentp. 302
Hot-melt Extruder Typesp. 303
Comparison of HME Devices and Oral Dosage Formsp. 305
HME Processes for Device Fabricationp. 306
Issues with HME in preparing Drug-eluting Devicesp. 308
Devices and Implantsp. 310
Anatomical Device Locationsp. 310
Simple Devicesp. 310
Non-medicated Prolonged Tissue Contact Devicesp. 312
Medicated (Drug-eluting) Prolonged Tissue Contact Devicesp. 313
Release Kineticsp. 318
Mechanisms of API Releasep. 318
Example In Vitro Drug Elution Profilesp. 319
Conclusionsp. 321
Referencesp. 321
Hot-melt Extrusion: An FDA Perspective on Product and Process Understandingp. 323
Introductionp. 323
Quality by Designp. 325
Utilizing QbD for HME Process Understandingp. 328
Referencesp. 331
Improved Process Understanding and Control of a Hot-melt Extrusion Process with Near-Infrared Spectroscopyp. 333
Vibrational Spectroscopy Introductionp. 333
Near-infrared Method Developmentp. 339
Near-infrared Probes and Fiber Opticsp. 344
NTR for Monitoring the Start-up of a HME Processp. 347
NIR for Improved Process Understanding and Controlp. 350
Referencesp. 353
Indexp. 355
Table of Contents provided by Ingram. All Rights Reserved.

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