Powell W S
Endocrine Laboratory, Royal Victoria Hospital, Montreal, Quebec, Canada.
Anal Biochem. 1987 Jul;164(1):117-31. doi: 10.1016/0003-2697(87)90375-7.
Prostaglandins, leukotrienes, and other metabolites of arachidonic acid can be conveniently and efficiently extracted from biological media using a precolumn containing octadecylsilyl silica connected to a 6-port switching valve that is in line with an analytical HPLC column. This procedure makes it possible to extract complex mixtures of eicosanoids and to analyze them by reversed-phase HPLC in a single step. The requirement to evaporate solvents from extracts prior to HPLC is therefore eliminated, saving time and reducing the possibilities for loss and contamination. The effects on recoveries of various media for loading the sample onto the precolumn were investigated, and it was concluded that 15% methanol at neutral pH gives the best overall results. It is therefore not necessary to acidity the sample prior to extraction, which simplifies the procedure and improves the recoveries of acid-labile eicosanoids. Following extraction, eicosanoids can be introduced onto the HPLC column by changing the position of the 6-port switching valve. We have investigated several approaches to the analysis of complex mixtures of these products by reversed-phase HPLC. The best results were obtained using a ternary gradient with a non-end-capped column of octadecylsilyl silica. Metabolites of arachidonic acid other than peptido-leukotrienes were first eluted by increasing the concentrations of acetonitrile and methanol in the mobile phase, which contained a constant concentration of trifluoroacetic acid (0.001%). Peptido-leukotrienes were then eluted with a second gradient, in which the concentrations of acetonitrile and methanol were kept constant, but the concentration of trifluoroacetic acid was increased to 0.0091%. Leukotrienes C4, D4, and E4 appear as sharp peaks at the end of the chromatogram and are completely separated from other types of arachidonic acid metabolites.
前列腺素、白三烯以及花生四烯酸的其他代谢产物,可使用连接到六通切换阀的含有十八烷基硅烷硅胶的预柱,从生物介质中方便且高效地提取出来。该六通切换阀与一根分析型高效液相色谱(HPLC)柱串联。此方法能够提取类二十烷酸的复杂混合物,并通过反相HPLC一步完成分析。因此,无需在HPLC分析之前从提取物中蒸发溶剂,节省了时间,减少了损失和污染的可能性。研究了将各种介质的样品加载到预柱上对回收率的影响,得出结论:中性pH值的15%甲醇总体效果最佳。因此,在提取之前无需将样品酸化,这简化了操作程序,并提高了对酸不稳定的类二十烷酸的回收率。提取后,通过改变六通切换阀的位置,可将类二十烷酸引入HPLC柱。我们研究了几种通过反相HPLC分析这些产物复杂混合物的方法。使用含有未封尾的十八烷基硅烷硅胶柱的三元梯度洗脱,得到了最佳结果。除肽白三烯外的花生四烯酸代谢产物首先通过增加流动相中乙腈和甲醇的浓度进行洗脱,流动相中含有恒定浓度的三氟乙酸(0.001%)。然后用第二个梯度洗脱肽白三烯,其中乙腈和甲醇的浓度保持不变,但三氟乙酸的浓度增加到0.0091%。白三烯C4、D4和E4在色谱图末端呈现为尖锐峰,并且与其他类型的花生四烯酸代谢产物完全分离。