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Effect of mobile phase pH on the retention of nucleotides on different stationary phases for high-performance liquid chromatography

机译:流动相pH值对高效液相色谱法不同固定相上核苷酸保留的影响

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摘要

The main aim of the present investigation was to study the retention and separation of eight nucleotides with the use of seven stationary phases in RP HPLC mode. Two octadecyl columns were used; however, aminopropyl, alkylamide, cholesterol, alkyl-phosphate, and phenyl were also studied. Special attention was paid to the mobile phase buffer pH, since it appears that this factor is very influential in the case of chromatographic separation of nucleotides. The retention of nucleotides was greater for mobile phase pH 4.0 in comparison with pH 7.0 (except for octadecyl and phenyl packing). This is a consequence of protonization of polar groups present on the stationary phase surface. It was proved that aminopropyl, alkyl phosphate, alkylamide packing materials are not suitable for the resolution of nucleotides. On the other hand, cholesterol and phenyl stationary phases are alternatives for conventional octadecyl phases. Application of cholesterol packing allows separation of small, polar nucleotides, which is impossible to achieve in the case of octadecyl phase. Moreover, a phenyl support allows separation of nucleotides in a shorter time in comparison with octadecyl packing.
机译:本研究的主要目的是在RP HPLC模式下使用七个固定相研究八个核苷酸的保留和分离。使用了两个十八烷基柱。但是,还研究了氨基丙基,烷基酰胺,胆固醇,磷酸烷基酯和苯基。要特别注意流动相缓冲液的pH值,因为看来这一因素在色谱分离核苷酸的情况下非常有影响。与pH 7.0相比,流动相pH 4.0中核苷酸的保留更大(十八烷基和苯基填料除外)。这是存在于固定相表面上的极性基团质子化的结果。事实证明,氨基丙基,磷酸烷基酯,烷基酰胺填充材料不适合用于拆分核苷酸。另一方面,胆固醇和苯基固定相是常规十八烷基相的替代物。胆固醇填充的应用可以分离小的极性核苷酸,这在十八烷基相的情况下是不可能实现的。此外,与十八烷基堆积相比,苯基支持物允许在更短的时间内分离核苷酸。

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