Avdeef A, Berger C M
pION Inc., 5 Constitution Way, Woburn, MA 01801, USA.
Eur J Pharm Sci. 2001 Dec;14(4):281-91. doi: 10.1016/s0928-0987(01)00190-7.
The main objective of this study was to develop an effective potentiometric saturation titration protocol for determining the aqueous intrinsic solubility and the solubility-pH profile of ionizable molecules, with the specific aim of overcoming incomplete dissolution conditions, while attempting to shorten the data collection time. A modern theory of dissolution kinetics (an extension of the Noyes-Whitney approach) was applied to acid-base titration experiments. A thermodynamic method was developed, based on a three-component model, to calculate interfacial, diffusion-layer, and bulk-water reactant concentrations in saturated solutions of ionizable compounds perturbed by additions of acid/base titrant, leading to partial dissolution of the solid material. Ten commercial drugs (cimetidine, diltiazem hydrochloride, enalapril maleate, metoprolol tartrate, nadolol, propoxyphene hydrochloride, quinine hydrochloride, terfenadine, trovafloxacin mesylate, and benzoic acid) were chosen to illustrate the new titration methodology. It was shown that the new method is about 10 times faster in determining equilibrium solubility constants, compared to the traditional saturation shake-flask methods.
本研究的主要目的是开发一种有效的电位饱和滴定方案,用于测定可电离分子的水相固有溶解度和溶解度-pH曲线,具体目标是克服不完全溶解条件,同时试图缩短数据收集时间。一种现代溶解动力学理论(诺伊斯-惠特尼方法的扩展)应用于酸碱滴定实验。基于三组分模型开发了一种热力学方法,用于计算在添加酸/碱滴定剂使固体物质部分溶解从而受到扰动的可电离化合物饱和溶液中的界面、扩散层和本体水反应物浓度。选择了十种商业药物(西咪替丁、盐酸地尔硫䓬、马来酸依那普利、酒石酸美托洛尔、纳多洛尔、盐酸丙氧芬、盐酸奎宁、特非那定、甲磺酸妥氟沙星和苯甲酸)来说明新的滴定方法。结果表明,与传统的饱和摇瓶法相比,新方法在测定平衡溶解度常数方面快约10倍。