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...

Descripción completa

Detalles Bibliográficos
Autor principal: Levitt, David G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734790/
https://www.ncbi.nlm.nih.gov/pubmed/23800230
http://dx.doi.org/10.1186/2050-6511-14-34

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734790/
https://www.ncbi.nlm.nih.gov/pubmed/23800230
http://dx.doi.org/10.1186/2050-6511-14-34

Ejemplares similares