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Quantitative systems pharmacology : models and model-based systems with applications /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Manca, Davide (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Amsterdam, The Netherlands : Elsevier, [2018]
Colección:Computer-aided chemical engineering ; v. 42.
Temas:
Acceso en línea:Texto completo
Texto completo

MARC

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245 0 0 |a Quantitative systems pharmacology :  |b models and model-based systems with applications /  |c edited by Davide Manca. 
264 1 |a Amsterdam, The Netherlands :  |b Elsevier,  |c [2018] 
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490 1 |a Computer aided chemical engineering ;  |v volume 42 
500 |a Includes index. 
505 0 |a Front Cover; Quantitative Systems Pharmacology: Models and Model-Based Systems with Applications; Copyright; Contents; Contributors; Preface; Acknowledgments; Section 1: Introduction to quantitative systems pharmacology; Chapter 1: Quantitative systems pharmacology: Extending the envelope through systems engineering; 1. Introduction; 2. The emergence of QSP modeling; 2.1. Multiscale modeling: Beyond the drug target; 2.2. Modeling the disease state; 3. Modeling drug exposure and drug response at the systemic level; 4. Modeling biological and drug interactions at the molecular level 
505 8 |a 4.1. Omics data4.2. Genomics; 4.3. Transcriptomics; 4.4. Proteomics; 4.5. Metabolomics; 4.6. Omics network using pathway enrichment; 4.7. Case study: Pathway enrichment for synthetic MPL; 5. Summary of the model development process; 6. QSP in context; 6.1. Case study: Cortisol regulation in the context of environmental clues: Next challenges; 7. How systems engineering can enable QSP; 8. Final comments; Acknowledgments; References; Section 2: Modeling and applications of systemic pharmacokinetics and pharmacodynamics 
505 8 |a Chapter 2: An engineering oriented approach to physiologically based pharmacokinetic and pharmacodynamic modeling1. Introduction; 2. Classic compartmental pharmacokinetic models; 3. Physiologically based pharmacokinetic models; 3.1. Individualization of the pharmacokinetic prediction; 3.2. Model identification; 3.2.1. The rationale of model-assisted experiments; 3.2.2. Linearization method; 3.2.3. Monte Carlo method; 3.2.4. Bootstrap method; 3.2.5. A posteriori identifiability; 4. Introduction to pharmacodynamics; 5. Mathematical formulation of a PBPK model; 5.1. The PBPK model 
505 8 |a 5.1.1. Model parameters5.1.2. PK simulation; 6. Mathematical formulation of PD models; 6.1. Direct effect model: Hill equation; 6.2. Indirect response models; 6.3. Irreversible effect models; 7. Conclusions; References; Chapter 3: Advanced Techniques for the Optimal Design of Experiments in Pharmacokinetics; 1. Introduction; 2. Identifying a physiological model: The need for experimental design; 3. Design of experiments under constraints for physiological models; 3.1. Design procedure; 3.2. Design of experimental protocols under uncertainty; 4. Case study I: Identification of a PK-PD model 
505 8 |a 5. Case study II: Design of more effective clinical tests for the study of VWD6. Conclusions; References; Chapter 4: On the Identifiability of Physiological Models: Optimal Design of Clinical Tests; 1. Introduction; 2. The concept of identifiability; 3. Identifiability tests; 3.1. A priori tests for parametric identifiability; 3.2. A posteriori tests for parametric identifiability; 3.3. Practical identifiability of parametric models; 4. Identifiability in the development of compartmental models; 5. Optimal design of clinical tests for guaranteed identifiability 
588 0 |a Online resource; title from digital title page (viewed on September 04, 2018). 
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650 0 |a Systems engineering. 
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700 1 |a Manca, Davide,  |e editor. 
776 0 8 |i Print version:  |t Quantitative systems pharmacology.  |d Amsterdam, The Netherlands : Elsevier, [2018]  |z 9780444639646  |z 0444639640  |w (OCoLC)1002834850 
830 0 |a Computer-aided chemical engineering ;  |v v. 42. 
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