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Computational Pharmacokinetics

Autor Anders Kallen
en Limba Engleză Hardback – 19 iul 2007
Being that pharmacokinetics (PK) is the study of how the body handles various substances, it is not surprising that PK plays an important role in the early development of new drugs. However, the clinical research community widely believes that mathematics in some way blurs the true meaning of PK. Demonstrating that quite the opposite is true, Computational Pharmacokinetics outlines the fundamental concepts and models of PK from a mathematical perspective based on clinically relevant parameters.

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.
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Specificații

ISBN-13: 9781420060652
ISBN-10: 1420060651
Pagini: 186
Ilustrații: 43 b/w images, 10 tables and 1000 equations
Dimensiuni: 156 x 234 x 15 mm
Greutate: 0.51 kg
Ediția:1
Editura: CRC Press
Colecția Chapman and Hall/CRC

Public țintă

Professional Practice & Development

Cuprins

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.