A Chemometric Strategy for Simultaneous Determination of Cholesterol andCholestanol in Human Serum Samples

Ali R. Jalalv, Esmael Sanchooli
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Abstract

In this study, we have developed a novel and efficient method based on spectrophotometry in combination with first-order multivariate calibration for simultaneous quantification of cholesterol (CHL) and cholestanol (CHN) in human serum samples. Several multivariate calibration (MVC) models including partial least squares-1 (PLS- 1), principal component regression (PCR), classical least squares (CLS), orthogonal signal correction-PLS-1, net analyte preprocessing-PLS-1 (NAP/PLS-1), and OSC-CLS were constructed based on first-order spectrophotometric data for simultaneous quantification of CHL and CHN under simulated physiological conditions to select the best algorithm for analyzing real samples. The compositions of the calibration mixtures were selected according to a central composite design (CCD) and validated with an external validation set. The results confirmed the more superiority of PCR to other algorithms. The results of applying PCR for simultaneous quantification of CHL and CHN in human serum samples as real samples were also encouraging. It is expected that the suitable features of the developed method make it potentially advantageous for biosensing, and clinical applications.
同时测定人血清样品中胆固醇和胆固醇的化学计量学策略
在这项研究中,我们建立了一种基于分光光度法结合一阶多变量校准同时定量人血清样品中胆固醇(CHL)和胆固醇(CHN)的新方法。在模拟生理条件下,基于一阶分光光度法同时定量CHL和CHN,构建了偏最小二乘-1 (PLS- 1)、主成分回归(PCR)、经典最小二乘(CLS)、正交信号校正-PLS-1、净分析物预处理-PLS-1 (NAP/PLS-1)和OSC-CLS等多变量校正(MVC)模型,以选择最优算法分析真实样品。根据中心组合设计(CCD)选择校准混合物的组成,并通过外部验证集进行验证。结果证实了PCR比其他算法更具优越性。应用PCR同时定量人血清样品中CHL和CHN作为真实样品的结果也令人鼓舞。期望所开发方法的适当特征使其在生物传感和临床应用方面具有潜在的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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