Shalaeva Marina, Kenseth Jeremy, Lombardo Franco, Bastin Andrea
Pfizer Global Research and Development, Groton Laboratories, Groton, Connecticut 06340, USA.
J Pharm Sci. 2008 Jul;97(7):2581-606. doi: 10.1002/jps.21287.
Evaluation of a multiplexed capillary electrophoresis (CE) method for pK(a) measurements of organic compounds, including low solubility compounds, is presented. The method is validated on a set of 105 diverse compounds, mostly drugs, and results are compared to literature values obtained from multiple references. Two versions of the instrument in two different labs were used to collect data over a period of 3 years and inter-laboratory and inter-instrument variations are discussed. Twenty-four point aqueous and mixed cosolvent buffer systems were employed to improve the accuracy of pK(a) measurements. It has been demonstrated that the method allows direct pK(a) measurements in aqueous buffers for many compounds of low solubility, often unattainable by other methods. The pK(a) measurements of compounds with extremely low solubility using multiplexed CE with methanol/water cosolvent buffers are presented.
本文介绍了一种用于测量有机化合物(包括低溶解度化合物)pK(a)值的多重毛细管电泳(CE)方法的评估。该方法在一组105种不同化合物(主要是药物)上进行了验证,并将结果与从多个参考文献中获得的文献值进行了比较。在3年的时间里,使用两个不同实验室的两种版本的仪器收集数据,并讨论了实验室间和仪器间的差异。采用24点水性和混合共溶剂缓冲系统来提高pK(a)测量的准确性。结果表明,该方法能够在水性缓冲液中直接测量许多低溶解度化合物的pK(a)值,而这通常是其他方法无法实现的。本文还介绍了使用甲醇/水共溶剂缓冲液的多重CE对极低溶解度化合物的pK(a)测量。