Can membrane permeability of zwitterionic compounds be predicted by the solubility-diffusion model?-Reference-Cited by-同舟云学术

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Can membrane permeability of zwitterionic compounds be predicted by the solubility-diffusion model?

Published:2024-08 Issue: Volume:199 Page:106819
ISSN:0928-0987
Container-title:European Journal of Pharmaceutical Sciences
language:en
Short-container-title:European Journal of Pharmaceutical Sciences

Author:

Ebert Andrea^ORCID,Dahley Carolin

Publisher

Elsevier BV

Reference68 articles.

1. Functional characterization of peptide transporters in MDCKII-MDR1 cell line as a model for oral absorption studies;Agarwal;Int. J. Pharm.,2007

2. Development of a 7-Day, 96-Well Caco-2 permeability assay with high-throughput direct UV compound analysis;Alsenz;Pharm. Res.,2003

3. Absorption and Drug development: Solubility, permeability, and Charge State;Avdeef,2012

4. Leakiness and size exclusion of paracellular channels in cultured epithelial cell monolayers–interlaboratory comparison;Avdeef;Pharm. Res.,2010

5. Caco-2 permeability of weakly basic drugs predicted with the double-sink PAMPA pK flux a method ଝ;Avdeef;Eur. J. Pharm. Sci.,2005

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1. Food and bile micelle binding of zwitterionic antihistamine drugs;ADMET and DMPK;2024-08-29

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