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Understanding Drug Release and Absorption Mechanisms: A Physical and Mathematical Approach
 
 
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Understanding Drug Release and Absorption Mechanisms: A Physical and Mathematical Approach [Hardcover]

Mario Grassi (Author), Gabriele Grassi (Author), Romano Lapasin (Author), Italo Colombo (Author)

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Book Description

December 26, 2006 0849330874 978-0849330872
Demand for better reliability from drug delivery systems has caused designers and researchers to move away from trial-and-error approaches and toward model-based methods of product development. Developing such models requires cross-disciplinary physical, mathematical, and physiological knowledge. Combining these areas under a single cover, Understanding Drug Release and Absorption Mechanisms builds a firm understanding ofall elements needed to conceive, build, and implement successful models of drug release.

Written by experts with broad industrial and academic experience, this book discusses the underlying physical principles, shows how to build mathematical models based on these principles, and finally compares the resulting models with experimental results. The authors begin by introducing the basics of modeling, physiological details of gastrointestinal and dermal absorption pathways, rheology, mass transport and thermodynamics, dissolution and partitioning, as well as size effects on the dissolution of crystallites. From this baseline, the authors explore applications in drug release from various delivery systems, specifically matrix systems, microemulsions, and permeability through membranes.

Working systematically from theory to working models, Understanding Drug Release and Absorption Mechanisms: A Physical and Mathematical Approach demonstrates the steps involved in designing, building, and implementing realistic and reliable models of drug release without unrealistically simplifying the theoretical parameters.


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Inside This Book (learn more)
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
initial drug distribution, drug mass balance, wormy micelles, dissolution medium bulk, drug diffusion coefficient, dissolution medium volume, ith component belonging, drug disk, tensional state, hydrophilic excipients, assuming sink conditions, solid wettability, polyphase mixtures, drug flux, initial drug concentration, uniform drug distribution, drug dissolution, cylindrical matrix, drug release kinetics, theophylline release, matrix volume element, sparingly soluble drugs, drug partition coefficient, drug concentration profile, wettability problems
Key Phrases - Capitalized Phrases (CAPs): (learn more)
New York, Colloid Interface Sci, Marcel Dekker, John Wiley, Springer Verlag, Cell Biol, International Symposium, Academic Press, Control Release, Drug Dev, Rheology of Industrial Polysaccharides, Cambridge University Press, Faraday Trans, Marcell Dekker, Plenum Press, Controlled Release of Bioactive Materials, Fluka Chemika, Physical Chemistry of Surfaces, Carlo Erba, Experimental Model, Boca Raton, Controlled Release Society, Fluid Phase Equilib, University of Trieste, Biomedical Research
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