Quantitative Concepts in Drug Formulation and Absorption and their Relevance for Drug Delivery

Authors

  • Georgios Imanidis
  • Marc Sutter
  • Susanne Reitbauer
  • Susanne B. Kapitza
  • Peter van Hoogevest
  • Daniel Hummel
  • Beat Müller
  • Peter Lütolf

DOI:

https://doi.org/10.2533/000942906777675038

Keywords:

Absorption, Drug delivery, Formulation, Intestinal, Modeling, (trans)dermal

Abstract

A series of theoretical models is presented to describe the processes of drug release and absorption following non-invasive administration by the intestinal and the (trans)dermal route. These models are used to analyze experimental data and provide the means to test hypotheses about the involved mechanisms and influence factors. They thus strengthen the basic understanding of drug release and absorption and help establish quantitative relationships that are relevant for the prediction and control of drug delivery.

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Published

2006-02-23

How to Cite

[1]
G. Imanidis, M. Sutter, S. Reitbauer, S. B. Kapitza, P. van Hoogevest, D. Hummel, B. Müller, P. Lütolf, Chimia 2006, 60, 46, DOI: 10.2533/000942906777675038.