Bailey Hope P, Rutan Sarah C
Department of Chemistry, PO Box 842006, Virginia Commonwealth University, Richmond, VA 23284-2006, USA.
Chemometr Intell Lab Syst. 2011 Mar 15;106(1):131-141. doi: 10.1016/j.chemolab.2010.07.008.
Two-dimensional liquid chromatography (LC×LC) is quickly becoming an important technique for the analysis of complex samples, owing largely to the relatively high peak capacities attainable by this analytical technique. With the increase in the complexity of the sample comes a corresponding increase in the complexity of the collected data. Thus the need for chemometric methods capable of resolving and quantifying such data is ever more urgent in order to obtain the maximum information available from the data. To this end, we have developed a chemometric method that combines iterative key set factor analysis and multivariate curve resolution-alternating least squares analysis with a spectral selectivity constraint that is shown to be capable of resolving chromatographically rank deficient, non-multilinear data. (Spectrally rank deficient compounds can only be quantified if the peaks having the same spectra are chromatographically resolved.) Over 50 chromatographic peaks were found in a relatively small section of a LC×LC-diode array data set of replicate urine samples (a four-way data set) using the developed method. The relative concentrations for 34 of the 50 peaks were determined with % RSD values ranging from 0.09 % to 16 %.
二维液相色谱法(LC×LC)正迅速成为分析复杂样品的一项重要技术,这在很大程度上归功于该分析技术可实现的相对较高的峰容量。随着样品复杂性的增加,所采集数据的复杂性也相应增加。因此,为了从数据中获取最大可用信息,对能够解析和量化此类数据的化学计量学方法的需求变得更加迫切。为此,我们开发了一种化学计量学方法,该方法将迭代密钥集因子分析和多元曲线分辨交替最小二乘法分析与光谱选择性约束相结合,结果表明该方法能够解析色谱秩亏、非多线性数据。(只有当具有相同光谱的峰在色谱上得到分离时,光谱秩亏化合物才能被定量。)使用所开发的方法,在重复尿液样品的LC×LC - 二极管阵列数据集(一个四维数据集)的相对较小部分中发现了50多个色谱峰。测定了50个峰中34个峰的相对浓度,相对标准偏差(%RSD)值范围为0.09%至16%。