Computational Pharmacokinetics
Autor Anders Kallenen Limba Engleză Paperback – 19 sep 2019
After an introductory chapter, the book presents a noncompartmental approach to PK and discusses the numerical analysis of PK data, including a description of an absorption process through numerical deconvolution. The author then builds a simple physiological model to better understand PK volumes and compares this model to other methods. The book also introduces compartmental models, discusses their limitations, and creates a general-purpose type of model. The final chapter looks at the relationship between drug concentration and effect, known as PK/pharmacodynamics (PD) modeling.
With both a solid discussion of theory and the use of practical examples, this book will enable readers to thoroughly grasp the computational factors of PK modeling.
| Toate formatele și edițiile | Preț | Express |
|---|---|---|
| Paperback (1) | 482.13 lei 6-8 săpt. | |
| CRC Press – 19 sep 2019 | 482.13 lei 6-8 săpt. | |
| Hardback (1) | 698.31 lei 6-8 săpt. | |
| CRC Press – 19 iul 2007 | 698.31 lei 6-8 săpt. |
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Specificații
ISBN-13: 9780367388843
ISBN-10: 0367388847
Pagini: 188
Dimensiuni: 156 x 234 x 15 mm
Greutate: 0.48 kg
Ediția:1
Editura: CRC Press
Colecția Chapman and Hall/CRC
ISBN-10: 0367388847
Pagini: 188
Dimensiuni: 156 x 234 x 15 mm
Greutate: 0.48 kg
Ediția:1
Editura: CRC Press
Colecția Chapman and Hall/CRC
Public țintă
Professional Practice & DevelopmentCuprins
Introduction. Empirical Pharmacokinetics. Numerical Methods for PK Parameter Estimation. Physiological Aspects on Pharmacokinetics. Modeling the Distribution Process. PK/PD Modeling. References. Appendices. Index.
Descriere
This book outlines the fundamental concepts and models of pharmacokinetics (PK) from a mathematical perspective based on clinically relevant parameters. It covers the analysis of PK data, discusses several physiological aspects to help understand the concepts, and explains processes using real-life data from pharmaceuticals. In addition, the author looks at the relationship between drug concentration and effect, known as PK/pharmacodynamics (PD) modeling. This book will enable readers to thoroughly grasp the computational factors of PK modeling.