Quantitation of small intestinal permeability during normal human drug absorption
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Pharmacology
Link
http://link.springer.com/article/10.1186/2050-6511-14-34/fulltext.html
Reference61 articles.
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2. Zhao YH, Le J, Abraham MH, Hersey A, Eddershaw PJ, Luscombe CN, Butina D, Beck G, Sherborne B, Cooper I: Evaluation of human intestinal absorption data and subsequent derivation of a quantitative structure-activity relationship (QSAR) with the Abraham descriptors. J Pharm Sci. 2001, 90 (6): 749-784. 10.1002/jps.1031.
3. Amidon KS, Langguth P, Lennernas H, Yu L, Amidon GL: Bioequivalence of oral products and the biopharmaceutics classification system: science, regulation, and public policy. Clin Pharmacol Ther. 2011, 90 (3): 467-470. 10.1038/clpt.2011.109.
4. Dahan A, Lennernas H, Amidon GL: The fraction dose absorbed, in humans, and high jejunal human permeability relationship. Molecular pharmaceutics. 2012, 9 (6): 1847-1851. 10.1021/mp300140h.
5. Soderholm JD, Olaison G, Kald A, Tagesson C, Sjodahl R: Absorption profiles for polyethylene glycols after regional jejunal perfusion and oral load in healthy humans. Dig Dis Sci. 1997, 42 (4): 853-857. 10.1023/A:1018836803254.
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