Davis Joe M, Stoll Dwight R, Carr Peter W
Department of Chemistry and Biochemistry, Southern Illinois University Carbondale, Carbondale, Illinois 62901, USA.
Anal Chem. 2008 Nov 1;80(21):8122-34. doi: 10.1021/ac800933z. Epub 2008 Oct 8.
One of the basic tenets of comprehensive two-dimensional chromatography is that the total peak capacity is simply the product of the first- and second-dimension peak capacities. As formulated, the total peak capacity does not depend on the relative values of the individual dimensions but only on the product of the two. This concept is tested here for the experimentally realistic situation wherein the first-dimension separation is undersampled. We first propose that a relationship exists between the number of observed peaks in a two-dimensional separation and the effective peak capacity. We then show here for a range of reasonable total peak capacities (500-4000) and various contributions of peak capacity in each dimension (10-150) that the number of observed peaks is only slightly dependent on the relative contributions over a reasonable and realistic range in sampling times (equal to the first-dimension peak standard deviation, multiplied by 0.2-16). Most of this work was carried out under the assumption of totally uncorrelated retention times. For uncorrelated separations, the small deviations from the product rule are due to the "edge effect" of statistical overlap theory and a recently introduced factor that corrects for the broadening of first-dimension peaks by undersampling them. They predict that relatively more peaks will be observed when the ratio of the first- to the second-dimension peak capacity is much less than unity. Additional complications are observed when first- and second-dimension retention times show some correlation, but again the effects are small. In both cases, deviations from the product rule are measured by the relative standard deviations of the number of observed peaks, which are typically 10 or less. Thus, although the basic tenet of two-dimensional chromatography is not exact when the first dimension is undersampled, the deviations from the product rule are sufficiently small as to be unimportant in practical work. Our results show that practitioners have a high degree of flexibility in designing and optimizing experimental comprehensive two-dimensional separations.
全二维色谱的基本原理之一是,总峰容量仅仅是第一维和第二维峰容量的乘积。按照公式表述,总峰容量并不取决于各个维度的相对值,而仅取决于两者的乘积。在此,针对第一维分离采样不足这一实验现实情况,对该概念进行了验证。我们首先提出,二维分离中观察到的峰数与有效峰容量之间存在某种关系。然后在此表明,对于一系列合理的总峰容量(500 - 4000)以及每个维度中峰容量的各种贡献(10 - 150),在合理且现实的采样时间范围(等于第一维峰标准差乘以0.2 - 16)内,观察到的峰数仅略微依赖于相对贡献。这项工作大多是在保留时间完全不相关的假设下进行的。对于不相关的分离,与乘积规则的小偏差是由于统计重叠理论的“边缘效应”以及最近引入的一个用于校正因采样不足导致的第一维峰展宽的因子。它们预测,当第一维与第二维峰容量之比远小于1时,将观察到相对更多的峰。当第一维和第二维保留时间显示出一定相关性时,会观察到其他复杂情况,但同样影响较小。在这两种情况下,与乘积规则的偏差通过观察到的峰数的相对标准偏差来衡量,其通常为10或更小。因此,尽管当第一维采样不足时,二维色谱的基本原理并不精确,但与乘积规则的偏差足够小,在实际工作中并不重要。我们的结果表明,从业者在设计和优化实验性全二维分离方面具有高度灵活性。