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Quantitation of small intestinal permeability during normal human drug absorption

BACKGROUND: Understanding the quantitative relationship between a drug’s physical chemical properties and its rate of intestinal absorption (QSAR) is critical for selecting candidate drugs. Because of limited experimental human small intestinal permeability data, approximate surrogates such as the f...

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Detalhes bibliográficos
Autor principal: Levitt, David G
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3734790/
https://ncbi.nlm.nih.gov/pubmed/23800230
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2050-6511-14-34
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