Cyclodextrins and the liquid-liquid phase distribution of progesterone, estrone and prednicarbate

被引:10
|
作者
Masson, Mar
Karlsson, Fridrik Jensen
Valdimarsdottir, Margret
Magnusdottir, Kristin
Loftsson, Thorsteinn
机构
[1] Univ Iceland, Fac Pharm, IS-107 Reykjavik, Iceland
[2] Univ Iceland, Dept Pharmacol & Toxicol, Fac Med, Reykjavik, Iceland
关键词
liquid-liquid partitioning; steroids; octanol-water; extraction; complexation;
D O I
10.1007/s10847-006-9238-3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The purpose of the present work was to investigate the interaction of drugs and octanol with hydroxypropyl beta- (HP beta CD) and gamma- (HP gamma CD) cyclodextrin, sulfobutyl ether beta-cyclodextrin (SBE beta CD) and randomly methylated-beta-cycoldextrin (RM beta CD) and to describe the interaction by theoretical models. The poorly soluble steroid drugs progesterone, estrone and prednicarbate were used as model compounds in this study. Hexane and chloroform were also investigated in combination with HP beta CD. Octanol formed a complex with all cyclodextrins and the saturation of the aqueous solution with this solvent therefore had a significant effect on the solubilization and extraction potential of cyclodextrins. Hexane had less affinity for cyclodextrins, but the drugs were poorly soluble in this solvent and it could therefore not be used in phase-distribution investigations. Previously we have derived equations that can be used to account for the competitive interaction between two guest compounds that compete for space in the cyclodextrin cavity. These equations were rearranged to calculate the complexation efficacy from phase-solubility data. An equation was derived that obtains intrinsic solubility (S (0)) and intrinsic partition coefficient (P) from the slopes of the phase-solubility and phase-distribution profiles. Investigation of the data showed that the results could not be sufficiently explained by the "classical" drug/cyclodextrin complex model that recognizes the possibility of competitive interactions but ignores any contribution from higher order complexes or aggregation of the cyclodextrin complexes. Relative difference in solubilization potential of different cyclodextrins cannot be translated to relative differences in extraction efficacy. Thus, for these three steroid compounds, RM beta CD and SBE beta CD gave the best solubilization potential whereas the best extraction efficacy was observed with HP gamma CD.
引用
收藏
页码:481 / 487
页数:7
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