Baczek Tomasz, Kaliszan Roman, Novotná Katerina, Jandera Pavel
Department of Biopharmaceutics and Pharmacodynamics, Faculty of Pharmacy, Medical University of Gdańsk, Gen. J. Hallera 107, 80 416 Gdańsk, Poland.
J Chromatogr A. 2005 May 20;1075(1-2):109-15. doi: 10.1016/j.chroma.2005.03.117.
The study was aimed at quantitative comparison of retention properties of modern stationary phases for reversed-phase HPLC. Three approaches, the calculated logarithm of octanol/water partition coefficient (clogP)-based model, the molecular modeling descriptors-based model and the hydrophobic-subtraction model, were compared and discussed. Gradient retention time, tR, of a series of test analytes was a dependent variable in the quantitative structure-retention relationship (QSRR) equations describing retention in terms of analytes' structure descriptors. The QSRRs derived were used to characterize in quantitative manner the specific retention properties of nine representative reversed-phase HPLC. Either the theoretically calculated logarithm of octanol/water partition coefficient, or the structural descriptors from molecular modeling were employed to quantitatively characterize the structure of the analytes. The three molecular modeling-derived structural descriptors considered were: the total dipole moment, the electron excess charge of the most negatively charged atom and the water-accessible molecular surface area. In addition to the above standard QSRR approaches, a recently developed parameterization of reversed-phase column selectivity based on the hydrophobic-subtraction model of Snyder et al. [L.R. Snyder, J.W. Dolan, J.W. Carr, The hydrophobic-subtraction model of reversed-phase column selectivity, J. Chromatogr. A 1060 (2004) 77] was considered. According to the hydrophobic-subtraction model, reversed-phase columns are characterized by five selectivity parameters derived from the linear solvation energy relationships (LSER) theory. Values of these parameters are available for more than 300 different columns. It has been demonstrated that the clogP-based model, the molecular modeling descriptors-based model and the hydrophobic-subtraction model provide generally similar classification of the HPLC columns studied. Some differences in column classification by the three approaches considered are discussed in terms of specific properties of individual stationary phases. All the approaches allow a quantitative, although multidimensional, characteristic of HPLC columns, however, the nonempirical QSRR-based approach is simpler and require less labor.
本研究旨在对反相高效液相色谱(HPLC)中现代固定相的保留特性进行定量比较。比较并讨论了三种方法,即基于辛醇/水分配系数计算对数(clogP)的模型、基于分子建模描述符的模型和疏水减法模型。一系列测试分析物的梯度保留时间tR是定量结构-保留关系(QSRR)方程中的因变量,该方程根据分析物的结构描述符来描述保留情况。所推导的QSRR用于以定量方式表征九种代表性反相HPLC的特定保留特性。采用理论计算的辛醇/水分配系数对数或分子建模得到的结构描述符来定量表征分析物的结构。所考虑的三个源自分子建模的结构描述符为:总偶极矩、最负电荷原子的电子过剩电荷和水可及分子表面积。除了上述标准QSRR方法外,还考虑了基于Snyder等人[L.R. Snyder, J.W. Dolan, J.W. Carr, The hydrophobic-subtraction model of reversed-phase column selectivity, J. Chromatogr. A 1060 (2004) 77]的疏水减法模型对反相柱选择性进行的最新参数化。根据疏水减法模型,反相柱由从线性溶剂化能关系(LSER)理论导出的五个选择性参数来表征。这些参数的值可用于300多种不同的色谱柱。结果表明,基于clogP的模型、基于分子建模描述符的模型和疏水减法模型对所研究的HPLC柱提供了大致相似的分类。根据各个固定相的特定性质,讨论了所考虑的三种方法在柱分类方面的一些差异。所有这些方法都能对HPLC柱进行定量(尽管是多维的)表征,然而,基于非经验QSRR的方法更简单且所需工作量更少。