Estimating drug solubility in the gastrointestinal tract

被引:167
作者
Dressman, J. B.
Vertzoni, M.
Goumas, K.
Reppas, C. [1 ]
机构
[1] Univ Athens, Dept Pharmaceut Technol, Athens 15771, Greece
[2] Goethe Univ Frankfurt, Dept Pharmaceut Technol, D-6000 Frankfurt, Germany
[3] Red Cross Hosp Athens, Dept Gastroenterol, Athens, Greece
关键词
solubility; gastrointestinal tract; humans; dogs; simulated media; oral absorption;
D O I
10.1016/j.addr.2007.05.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Solubilities measured in water are not always indicative of solubilities in the gastrointestinal tract. The use of aqueous solubility to predict oral drug absorption can therefore lead to very pronounced underestimates of the oral bioavailability, particularly for drugs which are poorly soluble and lipophilic. Mechanisms responsible for enhancing the luminal solubility of such drugs are discussed. Various methods for estimating intra-lumenal solubilities are presented, with emphasis on the two most widely implemented methods: determining solubility in fluids aspirated from the human gastrointestinal tract, and determining solubility in so-called biorelevant media, composed to simulate these fluids. The ability of the biorelevant media to predict solubility in human aspirates and to predict plasma profiles is illustrated with case examples. (c) 2007 Published by Elsevier B.V.
引用
收藏
页码:591 / 602
页数:12
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