Shayman J A, Barcelon F S
Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor.
J Chromatogr. 1990 Jun 8;528(1):143-54. doi: 10.1016/s0378-4347(00)82369-5.
A novel counter-ion, N-methylimipramine, was synthesized and utilized in the separation of inositol phosphates by ion-pair chromatography. The structural identity of the counter-ion was documented by nuclear magnetic resonance spectroscopy. This counter-ion was capable of resolving inositol phosphates isocratically by reversed-phase high-performance liquid chromatography. Solvent polarity and ionic strength markedly affected the retention of the polyphosphorylated inositides. pH, however, was less significant in its effects. Injection of inositol trisphosphate paired to N-methylimipramine into a mobile phase containing tetrabutylammonium ions demonstrated free exchange of the inositide between the counter-ions. This counter-ion may therefore prove useful in defining empirically the mechanisms of ion-pair chromatography.
合成了一种新型反离子N-甲基丙咪嗪,并将其用于离子对色谱法分离肌醇磷酸酯。通过核磁共振光谱确定了该反离子的结构特性。这种反离子能够通过反相高效液相色谱法等度分离肌醇磷酸酯。溶剂极性和离子强度对多磷酸化肌醇磷脂的保留有显著影响。然而,pH值的影响较小。将与N-甲基丙咪嗪配对的肌醇三磷酸注入含有四丁基铵离子的流动相中,结果表明肌醇磷脂在反离子之间可自由交换。因此,这种反离子可能有助于凭经验确定离子对色谱法的机制。