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Use of Semiselective TOCSY and the Pearson Correlation for the Metabonomic Analysis of Biofluid Mixtures: Application to Urine

机译:半选择性TOCSY和Pearson相关用于生物流体混合物的代谢组学分析:在尿液中的应用

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摘要

The authors recently proposed an approach to the metabonomic analysis of biofluid mixtures based on the use of the selective TOCSY experiment (Sandusky, P.; Raftery, D. Anal. Chem. 2005, 77, 2455). This method has some significant advantages over standard metabonomic analysis. However, when analyzing overlapped components, the selective TOCSY method can suffer from the relatively high likelihood of simultaneous excitation of several spin systems at once. This multiple excitation can cause problems both with the purity of the individual TOCSY peaks observed and with their assignment into specific spin systems. To address this problem, the possibility of using a more selective excitation is initially explored. Unfortunately, in most cases, greater spin system selectivity can only be gained at the expense of sensitivity. This is obviously an unacceptable tradeoff when dealing with biofluid samples. However, the application of the Pearson product moment correlation to the TOCSY peak integral intensities provides a test for individual TOCSY peak purity and allows for the assignment of the peaks into spin systems. The specific application of this two-stage "semiselective" TOCSY method to rat and human urine is presented. Significantly, it is also demonstrated that the use of semiselective TOCSY spectra as data inputs for PCA calculations provides a more sensitive and reliable method of distinguishing small differences in biofluid composition than the standard metabonomic approach using complete 1D proton NMR spectra of urine samples.
机译:作者最近提出了一种基于选择性TOCSY实验的生物流体混合物代谢组学分析方法(Sandusky,P。; Raftery,D.Anal.Chem。2005,77,2455)。与标准的代谢组学分析相比,该方法具有一些明显的优势。但是,当分析重叠的分量时,选择性TOCSY方法可能会同时激发多个自旋系统的可能性相对较高。这种多重激发可能会导致观察到的各个TOCSY峰的纯度以及将其分配给特定的自旋系统方面的问题。为了解决这个问题,最初探讨了使用更具选择性的激励的可能性。不幸的是,在大多数情况下,只能以牺牲灵敏度为代价才能获得更大的自旋系统选择性。当处理生物流体样品时,这显然是不可接受的折衷。但是,将皮尔逊乘积矩相关性应用于TOCSY峰积分强度可为单个TOCSY峰纯度提供测试,并允许将峰分配到自旋系统中。介绍了这种两阶段“半选择性” TOCSY方法在大鼠和人尿中的具体应用。重要的是,还证明了使用半选择性TOCSY光谱作为PCA计算的数据输入,比使用完整的尿液样品的一维质子NMR光谱的标准代谢组学方法提供了一种更灵敏,更可靠的方法来区分生物流体成分的细微差异。

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