Wang Xiaoli, Carr Peter W
AstraZeneca, PAR&D, Analytical Development, 1800 Concord Pike, Wilmington, DE 19803, USA.
J Chromatogr A. 2007 Jun 22;1154(1-2):165-73. doi: 10.1016/j.chroma.2007.03.057. Epub 2007 Mar 21.
Anionic species with ion pair forming ability are commonly used to enhance the retention and efficiency of basic analytes in RPLC separations. However, little is known about the interactions between organic mobile phase modifiers and such ion pairing anions. In this work, we measured the magnitude of the retention increase of basic drugs and peptides upon addition of strong inorganic ion pairing anions (e.g. perchlorate) as a function of the volume fraction of modifier in acidic water-acetonitrile mobile phases on two different stationary phases. We found that the increase in retention upon addition of various salts depended strongly on the eluent strength. In general, larger retention increases upon addition of the anion were observed at higher organic fractions. Regression of retention against the volume fraction of organic modifier indicated that the ion pair forming anions substantially decreased S values while only slightly changing ln k'w values. The decrease in S is the major cause of the retention increase of basic drugs and peptides when such anions are added to the mobile phase.
具有离子对形成能力的阴离子物种通常用于增强反相液相色谱(RPLC)分离中碱性分析物的保留时间和分离效率。然而,关于有机流动相改性剂与这种离子对阴离子之间的相互作用,人们了解甚少。在这项工作中,我们在两种不同的固定相上,测量了在酸性水 - 乙腈流动相中添加强无机离子对阴离子(如高氯酸盐)时,碱性药物和肽的保留增加幅度与改性剂体积分数的函数关系。我们发现,添加各种盐后保留时间的增加强烈依赖于洗脱液强度。一般来说,在较高有机分数下,添加阴离子后观察到的保留增加更大。保留时间与有机改性剂体积分数的回归表明,形成离子对的阴离子显著降低了S值,而对ln k'w值的影响很小。当将这种阴离子添加到流动相中时,S值的降低是碱性药物和肽保留增加的主要原因。