کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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202299 | 460597 | 2011 | 8 صفحه PDF | دانلود رایگان |
This study aims to measure the solubilities of poorly water-soluble drugs and to enhance their solubilities by adding co-solvents. The solubilities were measured using high-performance liquid chromatography (HPLC). We selected famotidine, a histamine H2-receptor antagonist, as the pharmaceutical compound. We measured the solubilities of famotidine at 298.15 K in five water/co-solvent mixed solvents, that is, two water + liquid co-solvent mixtures: water + ethanol, and water + polyethylene glycol (PEG) 400; and three water + solid co-solvent mixtures: water + β-cyclodextrin (β-CD), water + PEG 1000, and water + lauryl sulfate (SLS). In the two water + liquid co-solvent mixed solvents, the solubilities were measured over the entire co-solvent mole fraction range. In the three water + solid co-solvent mixtures, the solubility was determined up to the co-solvent saturation point. In addition, for the three solid co-solvents, i.e. β-CD, PEG 1000, and SLS, the solubilization power of each co-solvent–solute system was evaluated using a log-linear model. The experimental solubility data for the two water + liquid co-solvent mixtures were correlated using three local composition models: modified Wilson, NRTL 1, and UNIQUAC. For the three water + solid co-solvent mixtures, a modified Chrastil model was used to correlate the experimental solubility data.
Journal: Fluid Phase Equilibria - Volume 302, Issues 1–2, 15 March 2011, Pages 115–122