Trapp Oliver
Max-Planck-Institut für Kohlenforschung, Mülheim an der Ruhr, Germany.
Electrophoresis. 2006 Feb;27(3):534-41. doi: 10.1002/elps.200500708.
The unified equation was validated for first order reactions in dynamic CE with a data set of 31 250 elution profiles. Comparison with the results from conventional iterative computer simulation revealed that the unified equation is superior in terms of success rate and precision. The unified equation was applied to determine the cis-trans isomerization rate constants of the angiotensin converting enzyme inhibitor captopril. The separation of the rotational cis-trans isomeric drug has been performed in an aqueous 66 mM citric acid/Tris buffer at pH 3.0 in a 50 cm polyacrylamide-coated fused-silica capillary. Interconversion profiles featuring pronounced plateau formation and peak broadening were observed. Activation parameters DeltaH not equal and DeltaS not equal were obtained from temperature-dependent measurements between 10 and 25 degrees C in 2.5 K steps. From the activation parameters the isomerization barriers of captopril at 37 degrees C under acidic conditions were calculated to be DeltaG not equal trans-->cis=90.6 kJ/mol and DeltaG not equal cis-->trans=84.6 kJ/mol. By comparison of the kinetic data with the results obtained under basic conditions (pH 9.3) a mechanism of isomerization could be proposed.
利用包含31250个洗脱图谱的数据集,对动态毛细管电泳中一级反应的统一方程进行了验证。与传统迭代计算机模拟结果相比,统一方程在成功率和精度方面更具优势。该统一方程被用于测定血管紧张素转换酶抑制剂卡托普利的顺反异构化速率常数。在一根50 cm长的聚丙烯酰胺涂层熔融石英毛细管中,于pH 3.0的66 mM柠檬酸/Tris缓冲水溶液中对该旋转顺反异构药物进行了分离。观察到了具有明显平台形成和峰展宽的相互转化图谱。在10至25℃之间,以2.5 K步长进行温度依赖性测量,得到了活化参数ΔH≠和ΔS≠。根据这些活化参数,计算出酸性条件下37℃时卡托普利的异构化能垒为ΔG≠反式→顺式 = 90.6 kJ/mol和ΔG≠顺式→反式 = 84.6 kJ/mol。通过将动力学数据与在碱性条件(pH 9.3)下获得的结果进行比较,提出了一种异构化机制。