Biopharmaceutics Modeling and Simulations (ePub)
Theory, Practice, Methods, and Applications
(Sprache: Englisch)
A comprehensive introduction to using modeling and simulation
programs in drug discovery and development
Biopharmaceutical modeling has become integral to the design and
development of new drugs. Influencing key aspects of the
development process,...
programs in drug discovery and development
Biopharmaceutical modeling has become integral to the design and
development of new drugs. Influencing key aspects of the
development process,...
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A comprehensive introduction to using modeling and simulation
programs in drug discovery and development
Biopharmaceutical modeling has become integral to the design and
development of new drugs. Influencing key aspects of the
development process, including drug substance design, formulation
design, and toxicological exposure assessment, biopharmaceutical
modeling is now seen as the linchpin to a drug's future success.
And while there are a number of commercially available software
programs for drug modeling, there has not been a single resource
guiding pharmaceutical professionals to the actual tools and
practices needed to design and test safe drugs.
A guide to the basics of modeling and simulation programs,
Biopharmaceutics Modeling and Simulations offers
pharmaceutical scientists the keys to understanding how they work
and are applied in creating drugs with desired medicinal
properties. Beginning with a focus on the oral absorption of drugs,
the book discusses:
* The central dogma of oral drug absorption (the interplay of
dissolution, solubility, and permeability of a drug), which forms
the basis of the biopharmaceutical classification system (BCS)
* The concept of drug concentration
* How to simulate key drug absorption processes
* The physiological and drug property data used for
biopharmaceutical modeling
* Reliable practices for reporting results
With over 200 figures and illustrations and a peerless
examination of all the key aspects of drug research--including
running and interpreting models, validation, and compound and
formulation selection--this reference seamlessly brings
together the proven practical approaches essential to developing
the safe and effective medicines of tomorrow.
programs in drug discovery and development
Biopharmaceutical modeling has become integral to the design and
development of new drugs. Influencing key aspects of the
development process, including drug substance design, formulation
design, and toxicological exposure assessment, biopharmaceutical
modeling is now seen as the linchpin to a drug's future success.
And while there are a number of commercially available software
programs for drug modeling, there has not been a single resource
guiding pharmaceutical professionals to the actual tools and
practices needed to design and test safe drugs.
A guide to the basics of modeling and simulation programs,
Biopharmaceutics Modeling and Simulations offers
pharmaceutical scientists the keys to understanding how they work
and are applied in creating drugs with desired medicinal
properties. Beginning with a focus on the oral absorption of drugs,
the book discusses:
* The central dogma of oral drug absorption (the interplay of
dissolution, solubility, and permeability of a drug), which forms
the basis of the biopharmaceutical classification system (BCS)
* The concept of drug concentration
* How to simulate key drug absorption processes
* The physiological and drug property data used for
biopharmaceutical modeling
* Reliable practices for reporting results
With over 200 figures and illustrations and a peerless
examination of all the key aspects of drug research--including
running and interpreting models, validation, and compound and
formulation selection--this reference seamlessly brings
together the proven practical approaches essential to developing
the safe and effective medicines of tomorrow.
Autoren-Porträt von Kiyohiko Sugano
KIYOHIKO SUGANO has over seventeen years of experience asa pharmaceutical industrial researcher with Chugai in Japan and
Pfizer in the United Kingdom. He has published extensively in
peer-reviewed journals and book chapters, focusing on
physicochemical profiling, drug permeability across biological
membranes, oral drug delivery, and predictive and computational
modeling.
Bibliographische Angaben
- Autor: Kiyohiko Sugano
- 2012, 1. Auflage, 528 Seiten, Englisch
- Verlag: John Wiley & Sons
- ISBN-10: 111835432X
- ISBN-13: 9781118354322
- Erscheinungsdatum: 31.07.2012
Abhängig von Bildschirmgröße und eingestellter Schriftgröße kann die Seitenzahl auf Ihrem Lesegerät variieren.
eBook Informationen
- Dateiformat: ePub
- Größe: 18 MB
- Mit Kopierschutz
Sprache:
Englisch
Kopierschutz
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