Erlandsson Bengt, Wittgren Bengt, Brinkmalm Gunnar
AstraZeneca R&D Södertälje, Analytical Development, SE-151 85 Södertälje, Sweden.
J Pharm Biomed Anal. 2003 Apr 1;31(5):845-58. doi: 10.1016/s0731-7085(02)00662-3.
An aqueous size exclusion chromatography (SEC) method for determination of the molar mass of poloxamers 188 and 407 has been developed as an alternative to the pharmacopoeia methods. During the development work two different columns and several different eluent compositions were investigated. With a PL-aquagel-OH column, non-exclusion behaviour was obtained. A TSKgel column gave good separation of both poloxamers. The best separation was obtained with an eluent consisting of sodium chloride (0.01 M)-methanol (90:10, v/v) on the TSKgel column. The method was shown to be linear within the elution time of the two poloxamers and to have acceptable precision. The results from the SEC method was compared to results obtained using SEC with online multi angle light scattering detection (MALS) and to results obtained with matrix-assisted laser desorption/ionisation mass spectrometry (MALDI-MS).
已开发出一种用于测定泊洛沙姆188和407摩尔质量的水性尺寸排阻色谱(SEC)方法,作为药典方法的替代方法。在开发过程中,研究了两种不同的色谱柱和几种不同的洗脱液组成。使用PL-aquagel-OH色谱柱时,出现了非排阻行为。TSKgel色谱柱对两种泊洛沙姆都有良好的分离效果。在TSKgel色谱柱上,使用由氯化钠(0.01 M)-甲醇(90:10,v/v)组成的洗脱液可获得最佳分离效果。该方法在两种泊洛沙姆的洗脱时间范围内呈线性,且具有可接受的精密度。将SEC方法的结果与使用在线多角度光散射检测(MALS)的SEC结果以及基质辅助激光解吸/电离质谱(MALDI-MS)的结果进行了比较。