Pruim Peter, Ohman Marcus, Huo Yuli, Schoenmakers Peter J, Kok Wim Th
Polymer-Analysis Group, Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Nieuwe Achtergracht 166, 1018 WV Amsterdam, The Netherlands.
J Chromatogr A. 2008 Oct 24;1208(1-2):109-15. doi: 10.1016/j.chroma.2008.08.069. Epub 2008 Aug 23.
For the separation of peptides with gradient-elution liquid chromatography a poly(butyl methacrylate-co-ethylene dimethacrylate) (BMA) monolithic capillary column was prepared and tested. The conditional peak capacity was used as a metric for the performance of this column, which was compared with a capillary column packed with C18-modified silica particles. The retention of the peptides was found to be smaller on the BMA column than on the particulate C18 column. To obtain the same retention in isocratic elution an approximately 15% (v/v) lower acetonitrile concentration had to be used in the mobile phase. The retention window in gradient elution was correspondingly smaller with the BMA column. The relation between peak width and retention under gradient conditions was studied in detail. It was found that in shallow gradients, with gradient times of 30min and more, the peak widths of the least retained compounds are strongly increased with the BMA column. This was attributed to the fact that these compounds migrate and elute with an unfavorable high retention factor. More retained compounds are eluted later in the gradient, but with a lower effective retention factor. With shallow gradients the peak capacity of the BMA column ( approximately 90) was clearly lower than that of a conventional packed column ( approximately 150). On the other hand, with steep gradients, when components elute with a low effective retention factor, the performance of the BMA column is relatively good. With a gradient time of 15min similar peak widths and thus similar peak capacities ( approximately 75) were found for the packed and the monolithic column. Two strategies were investigated to obtain higher peak capacities with methacrylate monolithic columns. The use of lauryl methacrylate (LMA) instead of butyl methacrylate (BMA) gave an increase in retention and narrower peaks for early eluting peptides. The peak capacity of the LMA column was approximately 125 in a 60min gradient. Another approach was to use a longer BMA column which resulted in a peak capacity of approximately 135 could be obtained in 60min.
为了用梯度洗脱液相色谱法分离肽段,制备并测试了聚(甲基丙烯酸丁酯 - 二甲基丙烯酸乙烯酯)(BMA)整体式毛细管柱。使用条件峰容量作为该柱性能的衡量指标,并与填充C18改性硅胶颗粒的毛细管柱进行比较。发现肽段在BMA柱上的保留比在颗粒状C18柱上小。为了在等度洗脱中获得相同的保留,流动相中乙腈浓度必须降低约15%(v/v)。BMA柱在梯度洗脱中的保留窗口相应较小。详细研究了梯度条件下峰宽与保留之间的关系。发现在梯度时间为30分钟及更长的浅梯度中,保留最少的化合物在BMA柱上的峰宽会大幅增加。这归因于这些化合物以不利的高保留因子迁移和洗脱。保留更多的化合物在梯度后期洗脱,但有效保留因子较低。在浅梯度下,BMA柱的峰容量(约90)明显低于传统填充柱(约150)。另一方面,在陡梯度下,当组分以低有效保留因子洗脱时,BMA柱的性能相对较好。在梯度时间为15分钟时,填充柱和整体柱的峰宽相似,因此峰容量也相似(约75)。研究了两种策略以提高甲基丙烯酸酯整体柱的峰容量。使用甲基丙烯酸月桂酯(LMA)代替甲基丙烯酸丁酯(BMA)可增加早期洗脱肽段的保留并使峰变窄。在60分钟梯度中,LMA柱的峰容量约为125。另一种方法是使用更长的BMA柱,在60分钟内可获得约135的峰容量。