Kramer Kirsten E, Small Gary W
Optical Science and Technology Center and Department of Chemistry, University of Iowa, Iowa City, IA 52242, USA.
Appl Spectrosc. 2007 May;61(5):497-506. doi: 10.1366/000370207780807777.
An updating procedure is described for improving the robustness of multivariate calibration models based on near-infrared spectroscopy. Employing a single blank sample containing no analyte, repeated spectra are acquired during the instrumental warm-up period. These spectra are used to capture the instrumental profile on the analysis day in a way that can be used to update a previously computed calibration model. By augmenting the original spectra of the calibration samples with a group of spectra collected from the blank sample, an updated model can be computed that incorporates any instrumental drift that has occurred. This protocol is evaluated in the context of an analysis of physiological levels of glucose in a simulated biological matrix designed to mimic blood plasma. Employing data of calibration and prediction samples acquired over approximately six months, procedures are studied for implementing the algorithm in conjunction with calibration models based on partial least squares (PLS) regression. Over the range of 1-20 mM glucose, the final algorithm achieves a standard error of prediction (SEP) of 0.79 mM when the augmented PLS model is applied to data collected 176 days after the collection of the calibration spectra. Without updating, the original PLS model produces a seriously degraded SEP of 13.4 mM.
本文描述了一种更新程序,用于提高基于近红外光谱的多元校准模型的稳健性。使用一个不含分析物的单一空白样品,在仪器预热期间采集重复光谱。这些光谱用于捕捉分析当天的仪器特征,其方式可用于更新先前计算的校准模型。通过用从空白样品收集的一组光谱增强校准样品的原始光谱,可以计算出一个更新的模型,该模型包含了已发生的任何仪器漂移。在一个模拟生物基质中分析葡萄糖的生理水平的背景下评估了该方案,该模拟生物基质旨在模拟血浆。利用大约六个月内采集的校准和预测样品数据,研究了结合基于偏最小二乘(PLS)回归的校准模型实施该算法的程序。在1-20 mM葡萄糖范围内,当将增强的PLS模型应用于在校准光谱采集176天后收集的数据时,最终算法实现了0.79 mM的预测标准误差(SEP)。不进行更新时,原始PLS模型产生的SEP严重下降,为13.4 mM。