van der Maeden F P, van Rens P T, Buytenhuys F A, Buurman E
J Chromatogr. 1977 Nov 11;142:715-23. doi: 10.1016/s0021-9673(01)92079-5.
An improved quantitative analysis of d-tubocurarine chloride in the plant extract curare is presented. Gradient high-performance liquid chromatography on a hydrophobic stationary phase was found to be very suitable for the analysis of quaternary ammonium bases such as the complex mixture of curare alkaloids. Owing to the residual free silanol groups on the modified silica surface, the curare alkaloids are eluted from a reversed-phase column only if an electrolyte is added to the mobile phase. In order to optimize the separation, the effects of pH, the nature of the cation in the buffer and the concentration of the buffer of the retention of the alkaloids were investigated. Using a tetramethylammonium phosphate buffer at pH 4 in a gradient of water-methanol, undesirable retardation effects on the reversed-phase column could be suppressed sufficiently. As a result, an accurate method for the determination of d-tubocurarine chloride in curare was obtained. The coefficient of variation of this analysis is only 1.3%.
本文提出了一种对植物提取物箭毒中氯化筒箭毒碱的改进定量分析方法。结果发现,在疏水固定相上进行梯度高效液相色谱分析非常适合分析季铵碱,例如箭毒生物碱的复杂混合物。由于改性硅胶表面存在残留的游离硅醇基团,只有在流动相中添加电解质时,箭毒生物碱才能从反相柱上洗脱下来。为了优化分离效果,研究了pH值、缓冲液中阳离子的性质以及缓冲液浓度对生物碱保留的影响。在水 - 甲醇梯度中使用pH为4的磷酸四甲基铵缓冲液,可以充分抑制反相柱上不必要的拖尾效应。结果,获得了一种准确测定箭毒中氯化筒箭毒碱的方法。该分析方法的变异系数仅为1.3%。