Dissolution-Controlled Absorption is a pharmacokinetic absorption model in which the rate of drug entry into the systemic circulation is limited primarily by the compound's dissolution rate in the gastrointestinal fluid rather than by membrane permeability or transit kinetics.
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2017–2026
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31
Grzegorz Garbacz, Ralph‐Steven Wedemeyer, Stefan Nagel et al. · European Journal of Pharmaceutics and Biopharmaceutics · 2008 · 162 citations
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112
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4
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- MGMilo Gibaldi
University at Buffalo, State University of New York, United States
4 publications · 667 citations
4
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3
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3
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Columbia University
New York, United States
4 h-index
13 publications
2.1K citations
University of Michigan
Ann Arbor, United States
4 h-index
17 publications
919 citations
Johannes Gutenberg University Mainz
Mainz, Germany
4 h-index
12 publications
417 citations
University of Strathclyde
Glasgow, United Kingdom
2 h-index
4 publications
243 citations
Universitat de Miguel Hernández d'Elx
Elche, Spain
2 h-index
2 publications
59 citations
Setsunan University
Osaka, Japan
2 h-index
6 publications
488 citations
University of Kansas
Lawrence, United States
2 h-index
4 publications
50 citations
Universität Greifswald
Greifswald, Germany
1 h-index
5 publications
810 citations
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Venues
- Journal of Pharmaceutical Sciences
8 publications · 920 citations
8
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- European Journal of Pharmaceutics and Biopharmaceutics
EJPB · 3 publications · 221 citations
3
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- European Journal of Pharmaceutical Sciences
3 publications · 74 citations
3
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- Pharmaceutical Research
2 publications · 179 citations
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- International Journal of Pharmaceutics
2 publications · 43 citations
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