Schwarz M A, Neubert R H, Rüttinger H H
Institute of Pharmaceutics and Biopharmaceutics, Martin-Luther University, Halle/Saale, Germany.
J Chromatogr A. 1996 Sep 20;745(1-2):135-43. doi: 10.1016/0021-9673(96)00396-2.
Capillary electrophoresis offers a new way of characterizing interactions between different bile salts and drugs. The observed interactions were characterized with modified model functions known from affinity capillary electrophoresis (ACE) an micellar electrokinetic capillary electrophoresis (MECC). The methodical background of both methods is the change of the ionic mobility of the drug caused by partition between phases and aggregation with the bile salt molecules, respectively. This phenomenon is described by two different physicochemical models. A parameter estimation was carried out in order to obtain the partition coefficients KP as well as constants for the aggregate formation KA. Furthermore, an expression about the specific molar volume of the micelles and stoichiometric coefficients can be given.
毛细管电泳为表征不同胆汁盐与药物之间的相互作用提供了一种新方法。通过亲和毛细管电泳(ACE)和胶束电动毛细管电泳(MECC)中已知的改进模型函数对观察到的相互作用进行了表征。这两种方法的理论背景分别是药物在相之间分配以及与胆汁盐分子聚集导致的离子迁移率变化。这种现象由两种不同的物理化学模型描述。进行了参数估计以获得分配系数KP以及聚集体形成常数KA。此外,还可以给出关于胶束的比摩尔体积和化学计量系数的表达式。