Hollow Fiber-based Liquid-phase Microextraction and HPLC-UV Determination of Lovastatin in Biological Fluids

Author(s):
Fatemeh BayatFatemeh Bayat1, Atefeh BozorgiAtefeh Bozorgi2, 3,*
1Department of Medicinal Chemistry, Pharmaceutical Sciences Branch, Islamic Azad University, Tehran, Iran
2Department of Medicinal Chemistry, Faculty of Pharmacy, Alborz University of Medical Sciences, Karaj, Iran
3Evidence-based Phytotherapy and Complementary Medicine Research Center, Alborz University of Medical Sciences, Karaj, Iran
*Corresponding Author: Corresponding author: Department of Medicinal Chemistry, Faculty of Pharmacy, Alborz University of Medical Sciences, Shora Boulevard, Karaj, Alborz, Iran. Email:[email protected]

Journal of Reports in Pharmaceutical Sciences:Vol. 9, issue 2; 203-8
Published online:Oct 07, 2020
Article type:Research Article
Received:Jul 09, 2019
Accepted:May 19, 2020
How to Cite:Bayat F, Bozorgi A. Hollow Fiber-based Liquid-phase Microextraction and HPLC-UV Determination of Lovastatin in Biological Fluids. J Rep Pharm Sci. 2020;9(2):e147114. doi: https://doi.org/10.4103/jrptps.JRPTPS_71_19

Abstract

In this study, a hollow fiber liquid-phase microextraction (HF-LPME) method coupled with highperformance liquid chromatography (HPLC) was successfully developed for the determination of trace levels of lovastatin in urine and plasma samples. Lovastatin was extracted from 15 mL of the acidic sample solution with a pH of 2 into an organic extracting solvent (n-octanol) impregnated in the pores of a hollow fiber and then back extracted into an acidified aqueous solution in the lumen of the hollow fiber. After extraction, 10 μL of the acceptor phase was injected into HPLC system. To obtain high extraction efficiency, the parameters affecting the HF-LPME, including pH of the sample and extractant phases, type of organic phase, ionic strength, stirring rate, extraction time, and temperature, were studied and optimized. Under the optimized conditions (solvent 1-octanol, pH = 2, 45 min stirring at 45°C with 750 rpm), the relative recovery percentage was 85.2–97, which shows the capability of the method to analyze the analyte concentration. This technique provided preconcentration factor 199, 185, and 170 for water, urine, and plasma, respectively. Good precisions values (with relative standard division ≤ 10.5%) were obtained. The results indicated that the HF-LPME method has an excellent cleanup capacity and a high preconcentration factor and could serve as a simple and sensitive method for monitoring the drug in biological samples. Keywords: Biological sample, 

Copyright

© 2020, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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