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Design and manufacture of pharmaceutical tablets / / Reynir Eyjolfsson
Design and manufacture of pharmaceutical tablets / / Reynir Eyjolfsson
Autore Eyjolfsson Reynir
Pubbl/distr/stampa London, England : , : AP, , 2015
Descrizione fisica 1 online resource (68 p.)
Disciplina 615.1
Soggetto topico Drugs - Dosage forms
Pharmaceutical industry
Tablets (Medicine)
Soggetto genere / forma Electronic books.
ISBN 0-12-802187-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Title Page; Copyright Page; Dedication; Contents; Preface; Abbreviations; Chapter One - Introduction; 1.1 - General considerations; 1.2 - Particle sizes; 1.3 - Excipients; 1.3.1 - Ac-Di-Sol SD-711; 1.3.2 - Aerosil 200; 1.3.3 - Avicel PH-102; 1.3.4 - Compactrol; 1.3.5 - Corn starch; 1.3.6 - Di-Tab; 1.3.7 - Eudragit RS PO; 1.3.8 - Magnesium stearate 5712; 1.3.9 - Mannitol 60; 1.3.10 - Methocel K4M Premium; 1.3.11 - Methocel K100M Premium; 1.3.12 - Methocel K100LV Premium; 1.3.13 - Pharmatose 150M; 1.3.14 - Polyplasdone XL-10; 1.3.15 - Povidone; 1.3.16 - Primojel; 1.3.17 - Pruv
1.3.18 - Sodium bicarbonate1.3.19 - Starch 1500; 1.3.20 - Stearic acid 2236; 1.3.21 - Sterotex K; 1.3.22 - Tablettose 80; 1.3.23 - Talc; 1.4 - Equipment; 1.5 - Mixing of pharmaceutical powders; 1.6 - Design of experiments; 1.6.1 - Introduction to statistical design of experiments - the two-level factorial; 1.6.1.1 - Introduction; 1.6.1.2 - Designed experiments; 1.6.1.3 - Basic considerations; 1.6.1.4 - Two-level factorials; 1.6.1.5 - Two-level fractional factorials; 1.6.2 - Response surface methodology (RSM); 1.6.2.1 - Introduction; 1.6.2.2 - RSM and a sieving process variable study
1.6.2.3 - RSM investigation of the properties of a three-component tablet formulationReferences; Chapter two - Conventional-Release (CR) Tablets; 2.1 - Low-dose tablet by direct compression (DC); 2.1.1 - Properties of active pharmaceutical ingredient (API); 2.1.2 - Design; 2.1.3 - Manufacturing method; 2.1.4 - Remarks; 2.2 - High-dose tablet by direct compression; 2.2.1 - Properties of active pharmaceutical ingredient; 2.2.2 - Design; 2.2.3 - Manufacturing method; 2.2.4 - Remarks; 2.3 - Low-solubility API, low-dose tablet by wet granulation (WG)
2.3.1 - Properties of active pharmaceutical ingredient2.3.2 - Design; 2.3.3 - Manufacturing method; 2.3.4 - Remarks; 2.4 - Soluble API, low-dose tablet by wet granulation; 2.4.1 - Properties of active pharmaceutical ingredient; 2.4.2 - Design; 2.4.3 - Manufacturing method; 2.4.4 - Remarks; 2.5 - Low-solubility API, high-dose tablet by wet granulation; 2.5.1 - Properties of active pharmaceutical ingredient; 2.5.2 - Design; 2.5.3 - Manufacturing method; 2.5.4 - Remarks; 2.6 - Soluble API, high-dose tablet by wet granulation; 2.6.1 - Properties of active pharmaceutical ingredient; 2.6.2 - Design
2.6.3 - Manufacturing method2.6.4 - Remarks; References; Chapter three - Slow-Release (SR) Tablets; 3.1 - Slow-release tablet using a lipophilic release control agent; 3.1.1 - Properties of active pharmaceutical ingredient (API); 3.1.2 - Design; 3.1.3 - Manufacturing method; 3.1.4 - Remarks; 3.2 - Slow-release tablet using Eudragit and Methocel as release control agents; 3.2.1 - Properties of active pharmaceutical ingredient; 3.2.2 - Design; 3.2.3 - Manufacturing method; 3.2.4 - Remarks; 3.3 - Slow-release tablet using a mixture of Methocels as release control agent
3.3.1 - Properties of active pharmaceutical ingredient
Record Nr. UNINA-9910459964503321
Eyjolfsson Reynir  
London, England : , : AP, , 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Design and manufacture of pharmaceutical tablets / / Reynir Eyjolfsson
Design and manufacture of pharmaceutical tablets / / Reynir Eyjolfsson
Autore Eyjolfsson Reynir
Pubbl/distr/stampa London, England : , : AP, , 2015
Descrizione fisica 1 online resource (68 p.)
Disciplina 615.1
Soggetto topico Drugs - Dosage forms
Pharmaceutical industry
Tablets (Medicine)
ISBN 0-12-802187-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Title Page; Copyright Page; Dedication; Contents; Preface; Abbreviations; Chapter One - Introduction; 1.1 - General considerations; 1.2 - Particle sizes; 1.3 - Excipients; 1.3.1 - Ac-Di-Sol SD-711; 1.3.2 - Aerosil 200; 1.3.3 - Avicel PH-102; 1.3.4 - Compactrol; 1.3.5 - Corn starch; 1.3.6 - Di-Tab; 1.3.7 - Eudragit RS PO; 1.3.8 - Magnesium stearate 5712; 1.3.9 - Mannitol 60; 1.3.10 - Methocel K4M Premium; 1.3.11 - Methocel K100M Premium; 1.3.12 - Methocel K100LV Premium; 1.3.13 - Pharmatose 150M; 1.3.14 - Polyplasdone XL-10; 1.3.15 - Povidone; 1.3.16 - Primojel; 1.3.17 - Pruv
1.3.18 - Sodium bicarbonate1.3.19 - Starch 1500; 1.3.20 - Stearic acid 2236; 1.3.21 - Sterotex K; 1.3.22 - Tablettose 80; 1.3.23 - Talc; 1.4 - Equipment; 1.5 - Mixing of pharmaceutical powders; 1.6 - Design of experiments; 1.6.1 - Introduction to statistical design of experiments - the two-level factorial; 1.6.1.1 - Introduction; 1.6.1.2 - Designed experiments; 1.6.1.3 - Basic considerations; 1.6.1.4 - Two-level factorials; 1.6.1.5 - Two-level fractional factorials; 1.6.2 - Response surface methodology (RSM); 1.6.2.1 - Introduction; 1.6.2.2 - RSM and a sieving process variable study
1.6.2.3 - RSM investigation of the properties of a three-component tablet formulationReferences; Chapter two - Conventional-Release (CR) Tablets; 2.1 - Low-dose tablet by direct compression (DC); 2.1.1 - Properties of active pharmaceutical ingredient (API); 2.1.2 - Design; 2.1.3 - Manufacturing method; 2.1.4 - Remarks; 2.2 - High-dose tablet by direct compression; 2.2.1 - Properties of active pharmaceutical ingredient; 2.2.2 - Design; 2.2.3 - Manufacturing method; 2.2.4 - Remarks; 2.3 - Low-solubility API, low-dose tablet by wet granulation (WG)
2.3.1 - Properties of active pharmaceutical ingredient2.3.2 - Design; 2.3.3 - Manufacturing method; 2.3.4 - Remarks; 2.4 - Soluble API, low-dose tablet by wet granulation; 2.4.1 - Properties of active pharmaceutical ingredient; 2.4.2 - Design; 2.4.3 - Manufacturing method; 2.4.4 - Remarks; 2.5 - Low-solubility API, high-dose tablet by wet granulation; 2.5.1 - Properties of active pharmaceutical ingredient; 2.5.2 - Design; 2.5.3 - Manufacturing method; 2.5.4 - Remarks; 2.6 - Soluble API, high-dose tablet by wet granulation; 2.6.1 - Properties of active pharmaceutical ingredient; 2.6.2 - Design
2.6.3 - Manufacturing method2.6.4 - Remarks; References; Chapter three - Slow-Release (SR) Tablets; 3.1 - Slow-release tablet using a lipophilic release control agent; 3.1.1 - Properties of active pharmaceutical ingredient (API); 3.1.2 - Design; 3.1.3 - Manufacturing method; 3.1.4 - Remarks; 3.2 - Slow-release tablet using Eudragit and Methocel as release control agents; 3.2.1 - Properties of active pharmaceutical ingredient; 3.2.2 - Design; 3.2.3 - Manufacturing method; 3.2.4 - Remarks; 3.3 - Slow-release tablet using a mixture of Methocels as release control agent
3.3.1 - Properties of active pharmaceutical ingredient
Record Nr. UNINA-9910787164003321
Eyjolfsson Reynir  
London, England : , : AP, , 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Design and manufacture of pharmaceutical tablets / / Reynir Eyjolfsson
Design and manufacture of pharmaceutical tablets / / Reynir Eyjolfsson
Autore Eyjolfsson Reynir
Pubbl/distr/stampa London, England : , : AP, , 2015
Descrizione fisica 1 online resource (68 p.)
Disciplina 615.1
Soggetto topico Drugs - Dosage forms
Pharmaceutical industry
Tablets (Medicine)
ISBN 0-12-802187-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Title Page; Copyright Page; Dedication; Contents; Preface; Abbreviations; Chapter One - Introduction; 1.1 - General considerations; 1.2 - Particle sizes; 1.3 - Excipients; 1.3.1 - Ac-Di-Sol SD-711; 1.3.2 - Aerosil 200; 1.3.3 - Avicel PH-102; 1.3.4 - Compactrol; 1.3.5 - Corn starch; 1.3.6 - Di-Tab; 1.3.7 - Eudragit RS PO; 1.3.8 - Magnesium stearate 5712; 1.3.9 - Mannitol 60; 1.3.10 - Methocel K4M Premium; 1.3.11 - Methocel K100M Premium; 1.3.12 - Methocel K100LV Premium; 1.3.13 - Pharmatose 150M; 1.3.14 - Polyplasdone XL-10; 1.3.15 - Povidone; 1.3.16 - Primojel; 1.3.17 - Pruv
1.3.18 - Sodium bicarbonate1.3.19 - Starch 1500; 1.3.20 - Stearic acid 2236; 1.3.21 - Sterotex K; 1.3.22 - Tablettose 80; 1.3.23 - Talc; 1.4 - Equipment; 1.5 - Mixing of pharmaceutical powders; 1.6 - Design of experiments; 1.6.1 - Introduction to statistical design of experiments - the two-level factorial; 1.6.1.1 - Introduction; 1.6.1.2 - Designed experiments; 1.6.1.3 - Basic considerations; 1.6.1.4 - Two-level factorials; 1.6.1.5 - Two-level fractional factorials; 1.6.2 - Response surface methodology (RSM); 1.6.2.1 - Introduction; 1.6.2.2 - RSM and a sieving process variable study
1.6.2.3 - RSM investigation of the properties of a three-component tablet formulationReferences; Chapter two - Conventional-Release (CR) Tablets; 2.1 - Low-dose tablet by direct compression (DC); 2.1.1 - Properties of active pharmaceutical ingredient (API); 2.1.2 - Design; 2.1.3 - Manufacturing method; 2.1.4 - Remarks; 2.2 - High-dose tablet by direct compression; 2.2.1 - Properties of active pharmaceutical ingredient; 2.2.2 - Design; 2.2.3 - Manufacturing method; 2.2.4 - Remarks; 2.3 - Low-solubility API, low-dose tablet by wet granulation (WG)
2.3.1 - Properties of active pharmaceutical ingredient2.3.2 - Design; 2.3.3 - Manufacturing method; 2.3.4 - Remarks; 2.4 - Soluble API, low-dose tablet by wet granulation; 2.4.1 - Properties of active pharmaceutical ingredient; 2.4.2 - Design; 2.4.3 - Manufacturing method; 2.4.4 - Remarks; 2.5 - Low-solubility API, high-dose tablet by wet granulation; 2.5.1 - Properties of active pharmaceutical ingredient; 2.5.2 - Design; 2.5.3 - Manufacturing method; 2.5.4 - Remarks; 2.6 - Soluble API, high-dose tablet by wet granulation; 2.6.1 - Properties of active pharmaceutical ingredient; 2.6.2 - Design
2.6.3 - Manufacturing method2.6.4 - Remarks; References; Chapter three - Slow-Release (SR) Tablets; 3.1 - Slow-release tablet using a lipophilic release control agent; 3.1.1 - Properties of active pharmaceutical ingredient (API); 3.1.2 - Design; 3.1.3 - Manufacturing method; 3.1.4 - Remarks; 3.2 - Slow-release tablet using Eudragit and Methocel as release control agents; 3.2.1 - Properties of active pharmaceutical ingredient; 3.2.2 - Design; 3.2.3 - Manufacturing method; 3.2.4 - Remarks; 3.3 - Slow-release tablet using a mixture of Methocels as release control agent
3.3.1 - Properties of active pharmaceutical ingredient
Record Nr. UNINA-9910817344203321
Eyjolfsson Reynir  
London, England : , : AP, , 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Developing solid oral dosage forms : pharmaceutical theory & practice / / edited by Yihong Qiu [and four others]
Developing solid oral dosage forms : pharmaceutical theory & practice / / edited by Yihong Qiu [and four others]
Edizione [Second edition.]
Pubbl/distr/stampa London, [England] : , : Academic Press, , 2017
Descrizione fisica 1 online resource (1,176 pages) : illustrations
Disciplina 615.19
Soggetto topico Solid dosage forms
Solid dosage forms - Research
Tablets (Medicine)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910150253103321
London, [England] : , : Academic Press, , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Pharmaceutical dosage forms Tablets
Pharmaceutical dosage forms Tablets
Edizione [3rd ed. /]
Pubbl/distr/stampa New York : , : Informa Healthcare USA, , 2008
Descrizione fisica 1 online resource (550 p.)
Disciplina 615/.1901
Altri autori (Persone) AugsburgerLarry L
HoagStephen W
Soggetto topico Tablets (Medicine)
Drugs - Dosage forms
Soggetto genere / forma Electronic books.
ISBN 0-429-19115-4
1-4200-2029-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Foreword; Preface; Contents; Contributors; Chapter 1. Mass Transfer from Solid Oral Dosage Forms; Chapter 2. Approaches for Improving Bioavailability of Poorly Soluble Drugs; Chapter 3. Aims and Objectives and of Experimental Design and Optimization in Formulation and Process Development; Chapter 4. Knowledge-based Systems and Other AI Applications for Tableting; Chapter 5. Direct Compression and the Role of Filler-binders; Chapter 6. Disintegrants in Tableting; Chapter 7. Lubricants, Glidants, and Antiadherents; Chapter 8. Surfactants and Colors in Tablets
Chapter 9. Orally Disintegrating Tablets and Related Tablet FormulationsChapter 10. Formulation Challenges: Multiple Vitamin and Mineral Dosage Forms; Chapter 11. Botanicals and Their Formulation into Oral Solid Dosage Forms; Chapter 12. Formulation of Specialty Tablets for Slow Oral Dissolution; Chapter 13. Formulation and Design of Veterinary Tablets; Chapter 14. Swellable and Rigid Matrices: Controlled Release Matrices with Cellulose Ethers; Chapter 15. Carrageenans in Solid Dosage Form Design; Chapter 16. Osmotic Systems; Chapter 17. Tableting of Multiparticulate Modified Release Systems
Back Cover
Altri titoli varianti Tablets
Record Nr. UNINA-9910455930603321
New York : , : Informa Healthcare USA, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Pharmaceutical dosage forms Tablets
Pharmaceutical dosage forms Tablets
Edizione [3rd ed. /]
Pubbl/distr/stampa New York : , : Informa Healthcare USA, , 2008
Descrizione fisica 1 online resource (320 p.)
Disciplina 615.1901
Altri autori (Persone) AugsburgerLarry L
HoagStephen W
Soggetto topico Tablets (Medicine)
Drugs - Dosage forms
Soggetto genere / forma Electronic books.
ISBN 0-429-11633-0
1-4200-2030-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Foreword; Preface; Contents; Contributors; Chapter 1. Tooling for Pharmaceutical Processing; Chapter 2. Tablet Press Instrumentation in the Research and Development Environment; Chapter 3. Pharmaceutical Manufacturing: Changes in Paradigms; Chapter 4. A Forward-Looking Approach to Process Scale-Up for Solid Dose Manufacturing; Chapter 5. Dissolution and Drug Release Testing; Chapter 6. Setting Dissolution Specifications; Chapter 7. Mechanical Strength of Tablets; Chapter 8. cGMPs for the 21st Century and ICH Quality Initiatives
Chapter 9. Intellectual Property, Patent, and Patenting Process in the Pharmaceutical IndustryChapter 10. Near-infrared Chemical Imaging for Characterizing Pharmaceutical Dosage Forms; Chapter 11. Surface Area, Porosity, and Related Physical Characteristics; Back Cover
Altri titoli varianti Tablets
Record Nr. UNINA-9910455928703321
New York : , : Informa Healthcare USA, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Pharmaceutical dosage forms Tablets
Pharmaceutical dosage forms Tablets
Edizione [3rd ed.]
Pubbl/distr/stampa New York : , : Informa Healthcare USA, , 2008
Descrizione fisica 1 online resource (648 p.)
Disciplina 615.1901
615/.1901
Altri autori (Persone) AugsburgerLarry L
HoagStephen W
Soggetto topico Drugs -- Dosage forms
Tablets (Medicine)
Pharmacy, Therapeutics, & Pharmacology
Health & Biological Sciences
Soggetto genere / forma Electronic books.
ISBN 0-429-11949-6
1-4200-2028-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Foreword; Preface; Contents; Contributors; Chapter 1. Principles of Sampling for Particulate Solids; Chapter 2. Particle and Powder Bed Properties; Chapter 3. Flow: General Principles of Bulk Solids Handling; Chapter 4. Blending and Blend Uniformity; Chapter 5. Milling; Chapter 6. Drying; Chapter 7. Spray Drying: Theory and Pharmaceutical Applications; Chapter 8. Pharmaceutical Granulation Processes, Mechanism, and the Use of Binders; Chapter 9. Dry Granulation; Chapter 10. The Preparation of Pellets by Extrusion/Spheronization; Chapter 11. Coating Processes and Equipment
Chapter 12. Aqueous Polymeric Film CoatingChapter 13. The Application of Thermal Analysis to Pharmaceutical Dosage Forms; Chapter 14. Preformulation Studies for Tablet Formulation Development; Chapter 15. Stability Kinetics; Chapter 16. Compaction Simulation; Chapter 17. Compression and Compaction; Back Cover
Altri titoli varianti Tablets
Record Nr. UNINA-9910455904603321
New York : , : Informa Healthcare USA, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Pharmaceutical dosage forms Tablets
Pharmaceutical dosage forms Tablets
Edizione [3rd ed. /]
Pubbl/distr/stampa New York : , : Informa Healthcare USA, , 2008
Descrizione fisica 1 online resource (550 p.)
Disciplina 615/.1901
Altri autori (Persone) AugsburgerLarry L
HoagStephen W
Soggetto topico Tablets (Medicine)
Drugs - Dosage forms
ISBN 0-429-19115-4
1-4200-2029-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Foreword; Preface; Contents; Contributors; Chapter 1. Mass Transfer from Solid Oral Dosage Forms; Chapter 2. Approaches for Improving Bioavailability of Poorly Soluble Drugs; Chapter 3. Aims and Objectives and of Experimental Design and Optimization in Formulation and Process Development; Chapter 4. Knowledge-based Systems and Other AI Applications for Tableting; Chapter 5. Direct Compression and the Role of Filler-binders; Chapter 6. Disintegrants in Tableting; Chapter 7. Lubricants, Glidants, and Antiadherents; Chapter 8. Surfactants and Colors in Tablets
Chapter 9. Orally Disintegrating Tablets and Related Tablet FormulationsChapter 10. Formulation Challenges: Multiple Vitamin and Mineral Dosage Forms; Chapter 11. Botanicals and Their Formulation into Oral Solid Dosage Forms; Chapter 12. Formulation of Specialty Tablets for Slow Oral Dissolution; Chapter 13. Formulation and Design of Veterinary Tablets; Chapter 14. Swellable and Rigid Matrices: Controlled Release Matrices with Cellulose Ethers; Chapter 15. Carrageenans in Solid Dosage Form Design; Chapter 16. Osmotic Systems; Chapter 17. Tableting of Multiparticulate Modified Release Systems
Back Cover
Altri titoli varianti Tablets
Record Nr. UNINA-9910780603203321
New York : , : Informa Healthcare USA, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Pharmaceutical dosage forms Tablets
Pharmaceutical dosage forms Tablets
Edizione [3rd ed.]
Pubbl/distr/stampa New York : , : Informa Healthcare USA, , 2008
Descrizione fisica 1 online resource (648 p.)
Disciplina 615.1901
615/.1901
Altri autori (Persone) AugsburgerLarry L
HoagStephen W
Soggetto topico Drugs -- Dosage forms
Tablets (Medicine)
Pharmacy, Therapeutics, & Pharmacology
Health & Biological Sciences
ISBN 0-429-11949-6
1-4200-2028-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Foreword; Preface; Contents; Contributors; Chapter 1. Principles of Sampling for Particulate Solids; Chapter 2. Particle and Powder Bed Properties; Chapter 3. Flow: General Principles of Bulk Solids Handling; Chapter 4. Blending and Blend Uniformity; Chapter 5. Milling; Chapter 6. Drying; Chapter 7. Spray Drying: Theory and Pharmaceutical Applications; Chapter 8. Pharmaceutical Granulation Processes, Mechanism, and the Use of Binders; Chapter 9. Dry Granulation; Chapter 10. The Preparation of Pellets by Extrusion/Spheronization; Chapter 11. Coating Processes and Equipment
Chapter 12. Aqueous Polymeric Film CoatingChapter 13. The Application of Thermal Analysis to Pharmaceutical Dosage Forms; Chapter 14. Preformulation Studies for Tablet Formulation Development; Chapter 15. Stability Kinetics; Chapter 16. Compaction Simulation; Chapter 17. Compression and Compaction; Back Cover
Altri titoli varianti Tablets
Record Nr. UNINA-9910780603403321
New York : , : Informa Healthcare USA, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Pharmaceutical dosage forms Tablets
Pharmaceutical dosage forms Tablets
Edizione [3rd ed. /]
Pubbl/distr/stampa New York : , : Informa Healthcare USA, , 2008
Descrizione fisica 1 online resource (320 p.)
Disciplina 615.1901
Altri autori (Persone) AugsburgerLarry L
HoagStephen W
Soggetto topico Tablets (Medicine)
Drugs - Dosage forms
ISBN 0-429-11633-0
1-4200-2030-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Foreword; Preface; Contents; Contributors; Chapter 1. Tooling for Pharmaceutical Processing; Chapter 2. Tablet Press Instrumentation in the Research and Development Environment; Chapter 3. Pharmaceutical Manufacturing: Changes in Paradigms; Chapter 4. A Forward-Looking Approach to Process Scale-Up for Solid Dose Manufacturing; Chapter 5. Dissolution and Drug Release Testing; Chapter 6. Setting Dissolution Specifications; Chapter 7. Mechanical Strength of Tablets; Chapter 8. cGMPs for the 21st Century and ICH Quality Initiatives
Chapter 9. Intellectual Property, Patent, and Patenting Process in the Pharmaceutical IndustryChapter 10. Near-infrared Chemical Imaging for Characterizing Pharmaceutical Dosage Forms; Chapter 11. Surface Area, Porosity, and Related Physical Characteristics; Back Cover
Altri titoli varianti Tablets
Record Nr. UNINA-9910780603303321
New York : , : Informa Healthcare USA, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui