Peng Liming, Farkas Tivadar
Phenomenex, 411 Madrid Avenue, Torrance, CA, USA.
J Chromatogr A. 2008 Feb 1;1179(2):131-44. doi: 10.1016/j.chroma.2007.11.048. Epub 2007 Nov 22.
The separation of basic compounds in high-pH mobile phases results in extended retention, excellent peak shapes and good chromatographic efficiency. A severe decrease in sensitivity with electrospray mass spectrometric detection in positive ion mode (ESI+-MS) is expected under conditions that suppress analyte ionization in solution. We compared the responses of a large number of various basic drugs covering a wide range of hydrophobic (log P 0.09 to 7.6) and basic character (pKa 6.8-10) in LC-ESI+-MS/MS in 0.1% formic acid in water and acetonitrile, to responses in 10mM ammonium hydrogencarbonate buffers of different pH (7.8-11), and acetonitrile. Contrary to common expectations, high-pH mobile phases do not affect negatively the responses of basic compounds in ESI+. Analyte responses and limits of detection are comparable, or most often better in high pH compared to acidic mobile phases.
在高pH值流动相中分离碱性化合物可实现保留时间延长、峰形优异且色谱效率良好。在抑制溶液中分析物电离的条件下,预计正离子模式(ESI+-MS)下的电喷雾质谱检测灵敏度会严重下降。我们比较了大量各种碱性药物在水和乙腈中含0.1%甲酸的LC-ESI+-MS/MS中的响应,以及在不同pH值(7.8 - 11)的10mM碳酸氢铵缓冲液和乙腈中的响应。这些碱性药物涵盖了广泛的疏水性(log P为0.09至7.6)和碱性特征(pKa为6.8 - 10)。与通常的预期相反,高pH值流动相不会对ESI+中碱性化合物的响应产生负面影响。与酸性流动相相比,分析物响应和检测限相当,或者在高pH值条件下大多时候更好。