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Pharmaceutical drug analysis [[electronic resource] ] : methodology - theory - instrumentation - pharmaceutical assays - cognote assays
Pharmaceutical drug analysis [[electronic resource] ] : methodology - theory - instrumentation - pharmaceutical assays - cognote assays
Autore Kar Ashutosh
Edizione [2nd ed.]
Pubbl/distr/stampa New Delhi, : New Age International (P) Ltd., Publishers, 2005
Descrizione fisica 1 online resource (554 p.)
Disciplina 600
Soggetto topico Drugs - Analysis
Drugs - Testing
Soggetto genere / forma Electronic books.
ISBN 1-282-12901-5
9786612129018
81-224-2718-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. General aspects -- pt. 2. Chemical methods -- pt. 3. Electrochemical methods -- pt. 4. Optical methods -- pt. 5. Assay methods based on separation techniques -- pt. 6. Miscellaneous methods.
Record Nr. UNINA-9910454705003321
Kar Ashutosh  
New Delhi, : New Age International (P) Ltd., Publishers, 2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Pharmaceutical drug analysis : methodology - theory - instrumentation - pharmaceutical assays - cognote assays / / Ashutosh Kar
Pharmaceutical drug analysis : methodology - theory - instrumentation - pharmaceutical assays - cognote assays / / Ashutosh Kar
Autore Kar Ashutosh
Edizione [Second edition.]
Pubbl/distr/stampa New Delhi, : New Age International (P) Ltd., Publishers, 2005
Descrizione fisica 1 online resource (554 pages)
Disciplina 600
Soggetto topico Drugs - Analysis
Drugs - Testing
ISBN 1-282-12901-5
9786612129018
81-224-2718-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. General aspects -- pt. 2. Chemical methods -- pt. 3. Electrochemical methods -- pt. 4. Optical methods -- pt. 5. Assay methods based on separation techniques -- pt. 6. Miscellaneous methods.
Record Nr. UNINA-9910777978903321
Kar Ashutosh  
New Delhi, : New Age International (P) Ltd., Publishers, 2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Pharmaceutical drug analysis : methodology - theory - instrumentation - pharmaceutical assays - cognote assays
Pharmaceutical drug analysis : methodology - theory - instrumentation - pharmaceutical assays - cognote assays
Autore Kar Ashutosh
Edizione [2nd ed.]
Pubbl/distr/stampa New Delhi, : New Age International (P) Ltd., Publishers, 2005
Descrizione fisica 1 online resource (554 pages)
Disciplina 600
Soggetto topico Drugs - Analysis
Drugs - Testing
ISBN 1-282-12901-5
9786612129018
81-224-2718-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. General aspects -- pt. 2. Chemical methods -- pt. 3. Electrochemical methods -- pt. 4. Optical methods -- pt. 5. Assay methods based on separation techniques -- pt. 6. Miscellaneous methods.
Record Nr. UNINA-9910811948603321
Kar Ashutosh  
New Delhi, : New Age International (P) Ltd., Publishers, 2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Preparative chromatography of fine chemicals and pharmaceutical agents [[electronic resource] /] / edited by Henner Schmidt-Traub
Preparative chromatography of fine chemicals and pharmaceutical agents [[electronic resource] /] / edited by Henner Schmidt-Traub
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2005
Descrizione fisica 1 online resource (488 p.)
Disciplina 615.1901
Altri autori (Persone) Schmidt-TraubH
Soggetto topico Chromatographic analysis
Drugs - Analysis
Soggetto genere / forma Electronic books.
ISBN 1-280-52078-7
9786610520787
3-527-60348-4
3-527-60590-8
Classificazione 540
CHE 232f
CIT 060f
CIT 220f
VG 7200
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Preparative Chromatography; Contents; Preface; List of Contributors; Notation; List of Abbreviations; 1 Introduction; 2 Fundamentals and General Terminology; 3 Columns, Packings and Stationary Phases; 4 Selection of Chromatographic Systems; 5 Process Concepts; 6 Modeling and Determination of Model Parameters; 7 Model Based Design and Optimization; 8 Chromatographic Reactors; 9 Advanced Control of Simulated Moving Bed Processes; Outlook; References; Appendix A; Appendix B: Data of Test Systems; Index
Record Nr. UNINA-9910144007103321
Weinheim, : Wiley-VCH, c2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Preparative chromatography of fine chemicals and pharmaceutical agents [[electronic resource] /] / edited by Henner Schmidt-Traub
Preparative chromatography of fine chemicals and pharmaceutical agents [[electronic resource] /] / edited by Henner Schmidt-Traub
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2005
Descrizione fisica 1 online resource (488 p.)
Disciplina 615.1901
Altri autori (Persone) Schmidt-TraubH
Soggetto topico Chromatographic analysis
Drugs - Analysis
ISBN 1-280-52078-7
9786610520787
3-527-60348-4
3-527-60590-8
Classificazione 540
CHE 232f
CIT 060f
CIT 220f
VG 7200
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Preparative Chromatography; Contents; Preface; List of Contributors; Notation; List of Abbreviations; 1 Introduction; 2 Fundamentals and General Terminology; 3 Columns, Packings and Stationary Phases; 4 Selection of Chromatographic Systems; 5 Process Concepts; 6 Modeling and Determination of Model Parameters; 7 Model Based Design and Optimization; 8 Chromatographic Reactors; 9 Advanced Control of Simulated Moving Bed Processes; Outlook; References; Appendix A; Appendix B: Data of Test Systems; Index
Record Nr. UNINA-9910830821003321
Weinheim, : Wiley-VCH, c2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Preparative chromatography of fine chemicals and pharmaceutical agents / / edited by Henner Schmidt-Traub
Preparative chromatography of fine chemicals and pharmaceutical agents / / edited by Henner Schmidt-Traub
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2005
Descrizione fisica 1 online resource (488 p.)
Disciplina 615.1901
Altri autori (Persone) Schmidt-TraubH
Soggetto topico Chromatographic analysis
Drugs - Analysis
ISBN 1-280-52078-7
9786610520787
3-527-60348-4
3-527-60590-8
Classificazione 540
CHE 232f
CIT 060f
CIT 220f
VG 7200
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Preparative Chromatography; Contents; Preface; List of Contributors; Notation; List of Abbreviations; 1 Introduction; 2 Fundamentals and General Terminology; 3 Columns, Packings and Stationary Phases; 4 Selection of Chromatographic Systems; 5 Process Concepts; 6 Modeling and Determination of Model Parameters; 7 Model Based Design and Optimization; 8 Chromatographic Reactors; 9 Advanced Control of Simulated Moving Bed Processes; Outlook; References; Appendix A; Appendix B: Data of Test Systems; Index
Record Nr. UNINA-9910877845503321
Weinheim, : Wiley-VCH, c2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Process understanding [[electronic resource] ] : for scale-up and manufacture of active ingredients / / edited by Ian Houson
Process understanding [[electronic resource] ] : for scale-up and manufacture of active ingredients / / edited by Ian Houson
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (371 p.)
Disciplina 004.3
660.28
Altri autori (Persone) HousonI. N (Ian N.)
Soggetto topico Drugs - Design
Pharmaceutical microbiology
Drugs - Analysis
Soggetto genere / forma Electronic books.
ISBN 3-527-65036-9
1-283-28330-1
9786613283306
3-527-63715-X
3-527-63716-8
3-527-63714-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Process Understanding; Contents; Preface; List of Contributors; 1 Quality by Design; 1.1 History; 1.2 Defining Product Design Requirements and Critical Quality Attributes; 1.3 The Role of Quality Risk Management in QbD; 1.4 Design Space and Control Strategy; 1.5 Quality Systems; References; 2 Route and Process Selection; 2.1 Introduction; 2.2 Route Evaluation; 2.3 Factors to Consider; 2.3.1 Timing; 2.3.2 Costs; 2.3.2.1 Removal of a Chromatography Step; 2.3.3 Safety, Health, and Environment (SHE); 2.3.3.1 Safer Processes; 2.3.3.2 Green Chemistry; 2.3.4 Legal; 2.3.5 Other Considerations
2.3.5.1 Throughput2.3.5.2 Solvents; 2.3.5.3 Raw Materials; 2.3.5.4 Intermediates; 2.4 Route Selection; 2.4.1 Sildenafil; 2.5 Process Selection; 2.5.1 Pregabalin; 2.5.2 NK1 Receptor Antagonist; 2.5.3 Data; 2.6 Summary; References; 3 Critical Stages of Safety Assessment in Process Design and Scale-Up; 3.1 Reaction Safety Concepts; 3.1.1 What Is the Hazard?; 3.1.2 The Critical Effects of Scale-Up on Thermal Behavior; 3.1.3 Safety Features of a Reaction; 3.1.4 Stages of Safety Assessment; 3.2 Pre-Laboratory Safety Studies; 3.2.1 Predicting Reaction Safety Characteristics
3.2.2 Selecting Inherently Safer Processing Conditions3.3 The Synergies of Safety and Optimization - Together; 3.3.1 Testing of Potentially Explosive Compounds; 3.3.2 Thermal Stability Assessment; 3.3.3 Reaction Thermodynamic, Kinetic, and Gas-Generation Quantification; 3.3.4 Developing Fault-Tolerant Processes - by Design; 3.4 Establishing a Reliable Basis of Safety for Scale-Up; 3.4.1 Hazardous Scenario Identification; 3.4.2 Determining the Consequences of Hazardous Scenarios; 3.4.3 Experimental Simulation - Adiabatic Calorimetry; 3.4.4 Specify and Implement Safety Measures
3.4.5 Large-Scale Production3.5 Flammability Hazards; 3.5.1 Assessing Pilot-Scale Flammability Hazards; 3.6 Summary; References; 4 Understanding the Reaction; 4.1 Introduction; 4.2 Process Complexity; 4.2.1 Number of Phases; 4.2.2 Physical and Dynamic Complexity; 4.2.2.1 Length Scales; 4.2.2.2 Time; 4.2.2.3 Solubility; 4.2.2.4 Density; 4.2.2.5 Rheology; 4.2.2.6 Heat Transfer; 4.2.2.7 Mass Transfer/Interfacial Area; 4.2.2.8 Mixing Time; 4.2.3 Chemical Complexity; 4.3 Topics for Data Acquisition; 4.4 Reaction Profiles; 4.5 Reaction Pictures; 4.6 Ionic Equilibria and Reaction Selectivity
4.6.1 Nitration4.6.2 Acylation; 4.6.3 Association Equilibria - Lithium Diethylamide (LDA); 4.7 Kinetics; 4.7.1 Order of Reaction; 4.8 Catalyzed Processes; 4.9 The Rate-Determining Step; 4.10 Mixing in Chemical Reactors; 4.11 Mixing Theory; 4.11.1 Mixing Regimes; 4.11.2 Micromixing; 4.11.3 Macromixing; 4.11.4 Mesomixing; 4.11.5 Determining Mixing Sensitivity in the Laboratory; 4.11.6 Comments on Scalability of Mixing; 4.12 Multiphase Processes; 4.13 Mass Transfer Theory; 4.13.1 Effect of Mass Transfer on Chemical Reaction Rates; 4.13.1.1 Chemical Rate-Limited Reaction
4.13.1.2 Mass Transfer Rate-Limited Reaction
Record Nr. UNINA-9910131029403321
Weinheim, Germany, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Process understanding [[electronic resource] ] : for scale-up and manufacture of active ingredients / / edited by Ian Houson
Process understanding [[electronic resource] ] : for scale-up and manufacture of active ingredients / / edited by Ian Houson
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (371 p.)
Disciplina 004.3
660.28
Altri autori (Persone) HousonI. N (Ian N.)
Soggetto topico Drugs - Design
Pharmaceutical microbiology
Drugs - Analysis
ISBN 3-527-65036-9
1-283-28330-1
9786613283306
3-527-63715-X
3-527-63716-8
3-527-63714-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Process Understanding; Contents; Preface; List of Contributors; 1 Quality by Design; 1.1 History; 1.2 Defining Product Design Requirements and Critical Quality Attributes; 1.3 The Role of Quality Risk Management in QbD; 1.4 Design Space and Control Strategy; 1.5 Quality Systems; References; 2 Route and Process Selection; 2.1 Introduction; 2.2 Route Evaluation; 2.3 Factors to Consider; 2.3.1 Timing; 2.3.2 Costs; 2.3.2.1 Removal of a Chromatography Step; 2.3.3 Safety, Health, and Environment (SHE); 2.3.3.1 Safer Processes; 2.3.3.2 Green Chemistry; 2.3.4 Legal; 2.3.5 Other Considerations
2.3.5.1 Throughput2.3.5.2 Solvents; 2.3.5.3 Raw Materials; 2.3.5.4 Intermediates; 2.4 Route Selection; 2.4.1 Sildenafil; 2.5 Process Selection; 2.5.1 Pregabalin; 2.5.2 NK1 Receptor Antagonist; 2.5.3 Data; 2.6 Summary; References; 3 Critical Stages of Safety Assessment in Process Design and Scale-Up; 3.1 Reaction Safety Concepts; 3.1.1 What Is the Hazard?; 3.1.2 The Critical Effects of Scale-Up on Thermal Behavior; 3.1.3 Safety Features of a Reaction; 3.1.4 Stages of Safety Assessment; 3.2 Pre-Laboratory Safety Studies; 3.2.1 Predicting Reaction Safety Characteristics
3.2.2 Selecting Inherently Safer Processing Conditions3.3 The Synergies of Safety and Optimization - Together; 3.3.1 Testing of Potentially Explosive Compounds; 3.3.2 Thermal Stability Assessment; 3.3.3 Reaction Thermodynamic, Kinetic, and Gas-Generation Quantification; 3.3.4 Developing Fault-Tolerant Processes - by Design; 3.4 Establishing a Reliable Basis of Safety for Scale-Up; 3.4.1 Hazardous Scenario Identification; 3.4.2 Determining the Consequences of Hazardous Scenarios; 3.4.3 Experimental Simulation - Adiabatic Calorimetry; 3.4.4 Specify and Implement Safety Measures
3.4.5 Large-Scale Production3.5 Flammability Hazards; 3.5.1 Assessing Pilot-Scale Flammability Hazards; 3.6 Summary; References; 4 Understanding the Reaction; 4.1 Introduction; 4.2 Process Complexity; 4.2.1 Number of Phases; 4.2.2 Physical and Dynamic Complexity; 4.2.2.1 Length Scales; 4.2.2.2 Time; 4.2.2.3 Solubility; 4.2.2.4 Density; 4.2.2.5 Rheology; 4.2.2.6 Heat Transfer; 4.2.2.7 Mass Transfer/Interfacial Area; 4.2.2.8 Mixing Time; 4.2.3 Chemical Complexity; 4.3 Topics for Data Acquisition; 4.4 Reaction Profiles; 4.5 Reaction Pictures; 4.6 Ionic Equilibria and Reaction Selectivity
4.6.1 Nitration4.6.2 Acylation; 4.6.3 Association Equilibria - Lithium Diethylamide (LDA); 4.7 Kinetics; 4.7.1 Order of Reaction; 4.8 Catalyzed Processes; 4.9 The Rate-Determining Step; 4.10 Mixing in Chemical Reactors; 4.11 Mixing Theory; 4.11.1 Mixing Regimes; 4.11.2 Micromixing; 4.11.3 Macromixing; 4.11.4 Mesomixing; 4.11.5 Determining Mixing Sensitivity in the Laboratory; 4.11.6 Comments on Scalability of Mixing; 4.12 Multiphase Processes; 4.13 Mass Transfer Theory; 4.13.1 Effect of Mass Transfer on Chemical Reaction Rates; 4.13.1.1 Chemical Rate-Limited Reaction
4.13.1.2 Mass Transfer Rate-Limited Reaction
Record Nr. UNINA-9910830235403321
Weinheim, Germany, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Process understanding : for scale-up and manufacture of active ingredients / / edited by Ian Houson
Process understanding : for scale-up and manufacture of active ingredients / / edited by Ian Houson
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (371 p.)
Disciplina 004.3
660.28
Altri autori (Persone) HousonI. N (Ian N.)
Soggetto topico Drugs - Design
Pharmaceutical microbiology
Drugs - Analysis
ISBN 3-527-65036-9
1-283-28330-1
9786613283306
3-527-63715-X
3-527-63716-8
3-527-63714-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Process Understanding; Contents; Preface; List of Contributors; 1 Quality by Design; 1.1 History; 1.2 Defining Product Design Requirements and Critical Quality Attributes; 1.3 The Role of Quality Risk Management in QbD; 1.4 Design Space and Control Strategy; 1.5 Quality Systems; References; 2 Route and Process Selection; 2.1 Introduction; 2.2 Route Evaluation; 2.3 Factors to Consider; 2.3.1 Timing; 2.3.2 Costs; 2.3.2.1 Removal of a Chromatography Step; 2.3.3 Safety, Health, and Environment (SHE); 2.3.3.1 Safer Processes; 2.3.3.2 Green Chemistry; 2.3.4 Legal; 2.3.5 Other Considerations
2.3.5.1 Throughput2.3.5.2 Solvents; 2.3.5.3 Raw Materials; 2.3.5.4 Intermediates; 2.4 Route Selection; 2.4.1 Sildenafil; 2.5 Process Selection; 2.5.1 Pregabalin; 2.5.2 NK1 Receptor Antagonist; 2.5.3 Data; 2.6 Summary; References; 3 Critical Stages of Safety Assessment in Process Design and Scale-Up; 3.1 Reaction Safety Concepts; 3.1.1 What Is the Hazard?; 3.1.2 The Critical Effects of Scale-Up on Thermal Behavior; 3.1.3 Safety Features of a Reaction; 3.1.4 Stages of Safety Assessment; 3.2 Pre-Laboratory Safety Studies; 3.2.1 Predicting Reaction Safety Characteristics
3.2.2 Selecting Inherently Safer Processing Conditions3.3 The Synergies of Safety and Optimization - Together; 3.3.1 Testing of Potentially Explosive Compounds; 3.3.2 Thermal Stability Assessment; 3.3.3 Reaction Thermodynamic, Kinetic, and Gas-Generation Quantification; 3.3.4 Developing Fault-Tolerant Processes - by Design; 3.4 Establishing a Reliable Basis of Safety for Scale-Up; 3.4.1 Hazardous Scenario Identification; 3.4.2 Determining the Consequences of Hazardous Scenarios; 3.4.3 Experimental Simulation - Adiabatic Calorimetry; 3.4.4 Specify and Implement Safety Measures
3.4.5 Large-Scale Production3.5 Flammability Hazards; 3.5.1 Assessing Pilot-Scale Flammability Hazards; 3.6 Summary; References; 4 Understanding the Reaction; 4.1 Introduction; 4.2 Process Complexity; 4.2.1 Number of Phases; 4.2.2 Physical and Dynamic Complexity; 4.2.2.1 Length Scales; 4.2.2.2 Time; 4.2.2.3 Solubility; 4.2.2.4 Density; 4.2.2.5 Rheology; 4.2.2.6 Heat Transfer; 4.2.2.7 Mass Transfer/Interfacial Area; 4.2.2.8 Mixing Time; 4.2.3 Chemical Complexity; 4.3 Topics for Data Acquisition; 4.4 Reaction Profiles; 4.5 Reaction Pictures; 4.6 Ionic Equilibria and Reaction Selectivity
4.6.1 Nitration4.6.2 Acylation; 4.6.3 Association Equilibria - Lithium Diethylamide (LDA); 4.7 Kinetics; 4.7.1 Order of Reaction; 4.8 Catalyzed Processes; 4.9 The Rate-Determining Step; 4.10 Mixing in Chemical Reactors; 4.11 Mixing Theory; 4.11.1 Mixing Regimes; 4.11.2 Micromixing; 4.11.3 Macromixing; 4.11.4 Mesomixing; 4.11.5 Determining Mixing Sensitivity in the Laboratory; 4.11.6 Comments on Scalability of Mixing; 4.12 Multiphase Processes; 4.13 Mass Transfer Theory; 4.13.1 Effect of Mass Transfer on Chemical Reaction Rates; 4.13.1.1 Chemical Rate-Limited Reaction
4.13.1.2 Mass Transfer Rate-Limited Reaction
Record Nr. UNINA-9910877251303321
Weinheim, Germany, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Reviews in pharmaceutical and biomedical analysis [[electronic resource] /] / editors, Paraskevas D. Tzanavaras & Constantinos K. Zacharis
Reviews in pharmaceutical and biomedical analysis [[electronic resource] /] / editors, Paraskevas D. Tzanavaras & Constantinos K. Zacharis
Pubbl/distr/stampa [S.l.], : Bentham e Books, [2010]
Descrizione fisica 1 online resource (160 p.)
Disciplina 600
Altri autori (Persone) TzanavarasParaskevas D
ZacharisConstantinos K
Soggetto topico Drugs - Analysis
Drug monitoring
Soggetto genere / forma Electronic books.
ISBN 1-60805-190-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 01 Title.pdf; 02 Cover Page; 03 eBooks End User License Agreement-Website; 05 Forward; 06 Preface; 07 List of contributors; 08 Chapter 1 _Andrade_; 09 Chapter 2 _Loukas_ revised; 10 Chapter 3 _Mauri_ revised; 11 Chapter 4 _Xu_ revised; 12 Chapter 5 _O'Kennedy_; 13 Chapter 6 _Kauffmann_; 14 Chapter 7 _Samanidou_ revised; 15 Chapter 8 _Starek_ revised; 16 Chapter 9 _Tan_ revised; 17 Chapter 10 _Li_; 18 INDEX
Record Nr. UNINA-9910458887603321
[S.l.], : Bentham e Books, [2010]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui