The effects of food on the dissolution of poorly soluble drugs in human and in model small intestinal fluids

被引:215
作者
Persson, EM
Gustafsson, AS
Carlsson, AS
Nilsson, RG
Knutson, L
Forsell, P
Hanisch, G
Lennernäs, H
Abrahamsson, B [1 ]
机构
[1] AstraZeneca R&D, Dept Preformulat & Biopharmaceut, S-43183 Molndal, Sweden
[2] Uppsala Univ, Dept Pharm, S-75123 Uppsala, Sweden
[3] AstraZeneca R&D, Dept DMPK & Bioanal, S-43183 Molndal, Sweden
[4] Univ Hosp, Dept Surg, S-75185 Uppsala, Sweden
关键词
bile acids; dissolution rate; food effects; poorly soluble drugs; solubility;
D O I
10.1007/s11095-005-8192-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. This study was conducted to determine the effect of food on drug solubility and dissolution rate in simulated and real human intestinal fluids (HIF). Methods. Dissolution rate obtained via the rotating disk method and saturation solubility studies were carried out in fed and fasted state HIF, fed dog (DIF), and simulated (FeSSIF) intestinal fluid for six aprotic low solubility drugs. The intestinal fluids were characterized with respect to physical-chemical characteristics and contents. Results. Fed HIF provided a 3.5- to 30-times higher solubility compared to fasted HIF and FeSSIF, whereas fed DIF corresponded well (difference of less than 30%) to fed HIF. The increased solubility of food could mainly be attributed to dietary lipids and bile acids. The dissolution rate was also 2 to 7 times higher in fed HIF than fasted HIF. This was well predicted by both DIF and FeSSIF (difference of less than 30%). Conclusions. Intestinal solubility is higher in fed state compared to fasted state. However, the dissolution rate does not increase to the same extent. Dog seems to be a good model for man with respect to dissolution in the small intestine after intake of a meal, whereas FeSSIF is a poorer means of determining intestinal saturation solubility in the fed state.
引用
收藏
页码:2141 / 2151
页数:11
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