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A Chemometric Strategy for Simultaneous Determination of Cholesterol and Cholestanol in Human Serum Samples | OMICS International | Abstract
ISSN: 2155-9872

Journal of Analytical & Bioanalytical Techniques
Open Access

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Research Article

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

Ali R. Jalalvand*

Department of Chemical Engineering, Faculty of Energy, Kermanshah University of Technology, Kermanshah, Iran

*Corresponding Author:
Ali R. Jalalvand
Department of Chemical Engineering
Faculty of Energy, Kermanshah University of Technology
Kermanshah, Iran
Tel: +988337267520
Fax: +988337244201
E-mail: ali.jalalvand1984@gmail.com

Received date: July 27, 2016; Accepted date: September 29, 2016; Published date: October 05, 2016

Citation: Ali R. Jalalvand (2016) A Chemometric Strategy for Simultaneous Determination of Cholesterol and Cholestanol in Human Serum Samples. J Anal Bioanal Tech 7: 337. doi: 10.4172/2155-9872.1000337

Copyright: © 2016 Ali R. Jalalvand. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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.

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