
Hot-Melt Extrusion Pharmaceutical Applications
by Douroumis, DennisBuy New
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Summary
Author Biography
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 Contributors | p. xv |
Preface | p. xvii |
Single-screw Extrusion: Principles | p. 1 |
Introduction | p. 1 |
Ideal Compounding | p. 2 |
Basics of the Single-screw Extruder | p. 3 |
Screw Feed Section | p. 5 |
Screw Compressor Section | p. 9 |
Screw Metering Section | p. 11 |
Mixers | p. 11 |
Limitations of Conventional Single-screw Mixers | p. 13 |
SSE Elongational Mixers | p. 13 |
Summary | p. 20 |
References | p. 21 |
Twin-screw Extruders for Pharmaceutical Hot-melt Extrusion: Technology, Techniques and Practices | p. 23 |
Introduction | p. 23 |
Extruder Types and Working Principle | p. 24 |
Individual Parts of a TSE | p. 25 |
Drive Unit | p. 25 |
Screws | p. 25 |
Screw Elements | p. 27 |
Distributive Flow Elements | p. 28 |
Discharge Feed Screw | p. 28 |
Barrel | p. 29 |
Downstreaming | p. 30 |
Individual Processing Sections of the TSE | p. 31 |
Feeding Section | p. 32 |
Conveying/Melting Section | p. 32 |
Mixing Section | p. 33 |
Venting Section | p. 33 |
Extrusion Section | p. 33 |
Feeding of Solids | p. 34 |
TSE Operating Parameters | p. 34 |
Filling Level | p. 36 |
Screw Speed | p. 36 |
Feed Rate | p. 37 |
Residence Time Distribution | p. 37 |
Effect of Screw Speed and Feed Rate on Melt Temperature | p. 39 |
Setting up an HME Process using QbD Principles | p. 40 |
Understanding Knowledge Space | p. 40 |
Denning Design Space | p. 40 |
Determining Control Space | p. 41 |
Summary | p. 42 |
References | p. 42 |
Hot-melt Extrusion Developments in the Pharmaceutical Industry | p. 43 |
Introduction | p. 43 |
Advantages of HME as Drug Delivery Technology | p. 44 |
Formulations used for HME Applications | p. 45 |
Active Pharmaceutical Ingredient | p. 46 |
Solid Dispersions | p. 48 |
Bioavailability Improvement | p. 49 |
Controlled Delivery Systems | p. 51 |
Plasticizers | p. 53 |
Characterization of Extrudates | p. 55 |
Thermal Analysis | p. 55 |
Atomic Force Microscopy | p. 56 |
Residence Time | p. 57 |
Spectroscopic Techniques | p. 57 |
X-ray Diffraction (XRD) | p. 58 |
Microscopy | p. 58 |
Drug Release | p. 58 |
Hot-melt Extruded Dosage Forms | p. 58 |
Oral Drag Delivery | p. 59 |
Films | p. 61 |
Vaginal Rings and Implants | p. 61 |
A View to the Future | p. 63 |
References | p. 64 |
Solubility Parameters for Prediction of Drug/Polymer Miscibility in Hot-melt Extruded Formulations | p. 71 |
Introduction | p. 71 |
Solid Dispersions | p. 72 |
Basic Assumptions for the Drug-polymer Miscibility Prediction | p. 77 |
Solubility and the Flory-Huggins Theory | p. 78 |
Miscibility Estimation of Drug and Monomers | p. 83 |
Summary | p. 89 |
References | p. 90 |
The Influence of Plasticizers in Hot-melt Extrusion | p. 93 |
Introduction | p. 93 |
Traditional Plasticizers | p. 94 |
Non-traditional Plasticizers | p. 95 |
Specialty Plasticizers | p. 104 |
Conclusions | p. 107 |
References | p. 108 |
Applications of Poly(meth)acrylate Polymers in Melt Extrusion | p. 113 |
Introduction | p. 113 |
Polymer Characteristics | p. 116 |
Chemical Structure and Molecular Weight | p. 116 |
Glass Transition Temperature | p. 119 |
Plasticizers | p. 120 |
Thermostability | p. 121 |
Viscosity | p. 122 |
Specific Heat Capacity | p. 124 |
Hygroscopicity | p. 126 |
Melt Extrusion of Poly(methacrylates) to Design Pharmaceutical Oral Dosage Forms | p. 128 |
Solubility Enhancement | p. 128 |
Bioavailability Enhancement of BCS Class IV Drugs | p. 132 |
Controlled Release | p. 135 |
Time-controlled-release Dosage Forms | p. 136 |
pH-dependent Release | p. 138 |
Taste Masking | p. 139 |
Summary | p. 140 |
References | p. 140 |
Hot-melt Extrusion of Ethylcellulose, Hypromellose and Polyethylene Oxide | p. 145 |
Introduction | p. 145 |
Background | p. 146 |
Thermal Properties | p. 147 |
Processing Aids/Additives | p. 147 |
Unconventional Processing Aids: Drags, Blends | p. 149 |
Case Studies | p. 151 |
Ethylcellulose | p. 151 |
Combinations of Excipients | p. 151 |
Solubilization | p. 155 |
Film | p. 159 |
Unique Dosage Forms | p. 163 |
Abuse Resistance | p. 163 |
Controlled Release | p. 164 |
Solubility Parameters | p. 166 |
Milling of EC, HPMC and PEO Extrudate | p. 168 |
References | p. 170 |
Bioadhesion Properties of Polymeric Films Produced by Hot-melt Extrusion | p. 177 |
Introduction | p. 177 |
Anatomy of the Oral Cavity and Modes of Drug Transport | p. 180 |
Structure | p. 180 |
Modes of Drug Transport and Kinetics | p. 180 |
Factors Affecting Drug Absorption | p. 181 |
Mucoadhesive Mechanisms | p. 182 |
Factors Affecting Mucoadhesion in the Oral Cavity | p. 183 |
Determination of Mucoadhesion and Mechanical Properties of Films | p. 183 |
Bioadhesive Films Prepared by HME | p. 184 |
Summary | p. 194 |
References | p. 194 |
Taste Masking Using Hot-melt Extrusion | p. 201 |
The Need and Challenges for Masking Bitter APIs | p. 201 |
Organization of the Taste System | p. 203 |
Taste Perception in Humans and Organization of Peripheral System | p. 203 |
Transduction of Taste Signals | p. 205 |
Taste Sensing Systems (Electronic Tongues) for Pharmaceutical Dosage Forms | p. 206 |
Alpha MOS Electronic Tongue: Instrumentation and Operational Principles | p. 206 |
Taste Analysis | p. 208 |
Taste Masking Efficiency Testing | p. 209 |
Advantages of E-tongue Taste Analysis | p. 211 |
Hot-melt Extrusion: An Effective Means of Taste Masking | p. 212 |
Taste Masking via Polymer Extrusion | p. 212 |
Taste Masking via Solid Lipid Extrusion | p. 216 |
Summary | p. 219 |
References | p. 219 |
Clinical and Preclinical Studies, Bioavailability and Pharmacokinetics of Hot-melt Extruded Products | p. 223 |
Introduction to Oral Absorption | p. 223 |
In Vivo Evaluation of Hot-melt Extruded Solid Dispersions | p. 225 |
Oral Immediate Release | p. 225 |
Oral Controlled Release | p. 232 |
Implants | p. 233 |
Conclusion | p. 234 |
References | p. 234 |
Injection Molding and Hot-melt Extrusion Processing for Pharmaceutical Materials | p. 239 |
Introduction | p. 239 |
Hot-melt Extrusion in Brief | p. 240 |
Injection Molding | p. 241 |
Critical Parameters | p. 242 |
Melt Temperature | p. 242 |
Barrel Temperature | p. 243 |
Cooling Temperature | p. 243 |
Holding Pressure | p. 243 |
Holding Time | p. 243 |
Back Pressure | p. 244 |
Injection Speed | p. 244 |
Cooling Time/Cycle Time | p. 244 |
Example: Comparison of Extruded and Injection-molded Material | p. 245 |
Development of Products for Injection Molding | p. 246 |
Excipients | p. 246 |
Stability | p. 248 |
Process Development | p. 248 |
Properties of Injection-molded Materials | p. 251 |
EgaletĀ® Technology | p. 251 |
Controlling Physical State by Means of Hot-melt Extrusion and Injection Molding | p. 253 |
Anti-tamper Properties of Injection-molded Tablets | p. 254 |
Concluding Remarks | p. 257 |
References | p. 257 |
Laminar Dispersive and Distributive Mixing with Dissolution and Applications to Hot-melt Extrusion | p. 261 |
Introduction | p. 261 |
Elementary Steps in HME | p. 263 |
Paniculate Solids Handling (PSH) | p. 263 |
Melting | p. 263 |
Devolatilization | p. 264 |
Pumping and Pressurization | p. 265 |
Dispersive and Distributive Mixing | p. 265 |
HME Processes: Cases I and II | p. 265 |
Case I | p. 266 |
Case II | p. 268 |
Dissolution of Drug Particulates in Polymeric Melt | p. 270 |
Process Variables | p. 270 |
Equipment Variables | p. 273 |
Material Variables | p. 275 |
Case Study: Acetaminophen and Poly(ethylene oxide) | p. 278 |
Determination of Solubility of APAP in PEO | p. 280 |
References | p. 282 |
Technological Considerations Related to Scale-up of Hot-melt Extrusion Processes | p. 285 |
Introduction | p. 285 |
Scale-up Terminology | p. 287 |
Scale-up: Batch Size | p. 287 |
Scale-up: Feed Rate | p. 288 |
Scale-up: Extruder Diameter | p. 290 |
Volumetric Scale-up | p. 290 |
Volumetric Scale-up: Length/Diameter (L/D) | p. 292 |
Volumetric Scale-up: Diameter Ratio | p. 292 |
Volumetric Scale-up: Screw Design | p. 294 |
Power Scale-up | p. 296 |
Heat Transfer Scale-up | p. 298 |
Die Scale-up | p. 299 |
Conclusion | p. 299 |
References | p. 300 |
Devices and Implant Systems by Hot-melt Extrusion | p. 301 |
Introduction | p. 301 |
HME in Device Development | p. 302 |
Hot-melt Extruder Types | p. 303 |
Comparison of HME Devices and Oral Dosage Forms | p. 305 |
HME Processes for Device Fabrication | p. 306 |
Issues with HME in preparing Drug-eluting Devices | p. 308 |
Devices and Implants | p. 310 |
Anatomical Device Locations | p. 310 |
Simple Devices | p. 310 |
Non-medicated Prolonged Tissue Contact Devices | p. 312 |
Medicated (Drug-eluting) Prolonged Tissue Contact Devices | p. 313 |
Release Kinetics | p. 318 |
Mechanisms of API Release | p. 318 |
Example In Vitro Drug Elution Profiles | p. 319 |
Conclusions | p. 321 |
References | p. 321 |
Hot-melt Extrusion: An FDA Perspective on Product and Process Understanding | p. 323 |
Introduction | p. 323 |
Quality by Design | p. 325 |
Utilizing QbD for HME Process Understanding | p. 328 |
References | p. 331 |
Improved Process Understanding and Control of a Hot-melt Extrusion Process with Near-Infrared Spectroscopy | p. 333 |
Vibrational Spectroscopy Introduction | p. 333 |
Near-infrared Method Development | p. 339 |
Near-infrared Probes and Fiber Optics | p. 344 |
NTR for Monitoring the Start-up of a HME Process | p. 347 |
NIR for Improved Process Understanding and Control | p. 350 |
References | p. 353 |
Index | p. 355 |
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