Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7381
Title: Ultrasound-assisted emulsification microextraction combined with ultra-high performance liquid chromatography-tandem mass spectrometry for the analysis of ibuprofen and its metabolites in human urine
Authors: Magiera, S.
Gülmez, Şefika
Keywords: Human urine
Ibuprofen
Metabolite
Ultra-high performance liquid chromatography
Ultrasound-assisted emulsification microextraction
1-Octanol
Chemical Fractionation
Chromatography, High Pressure Liquid
Humans
Limit of Detection
Tandem Mass Spectrometry
Ultrasonics
Abstract: In this study, a fast, simple and efficient method based on ultrasound-assisted emulsification-microextraction (USAEME) coupled with ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) was successfully developed for the determination of ibuprofen (IBU) and its four metabolites (1-hydroxyibuprofen (1-HIBU), 2-hydroxyibuprofen (2-HIBU), 3-hydroxyibuprofen (3-HIBU), carboxyibuprofen (CIBU)) in human urine. For this purpose, the influence of the different parameters affecting the USAEME procedure was evaluated in order to optimize the efficiency of the process. The optimum conditions were found to be: 100. µL of 1-octanol as extraction solvent, 2. mL of urine sample, 15% (w/v) NaCl to control the ionic strength, ultrasonication for 10. min; and centrifugation for 5. min at 6500. rpm. After sample preparation, chromatographic separation was achieved on a Zorbax Rapid Resolution High Definition (RRHD) SB-C18 column using the mobile phase consisting of 0.1% formic acid in water and acetonitrile in an elution gradient. Detection was performed in a triple quadrupole tandem mass spectrometer using the multiple reaction monitoring (MRM) mode and negative ionization.The proposed method showed satisfactory linearity over a wide concentration range (correlation coefficients over 0.9994). The lower limit of quantification (LLOQ) was 0.0005. ng/mL for IBU and its metabolites. The intra- and inter-day precisions were in the range of 2.19-10.8% and the accuracies were between -5.93% and 6.29%. The mean recovery of analytes ranged from 90.7 to 104%. As a result, this method has been successfully applied for the sensitive determination of IBU and its metabolites in human urine samples. © 2014 Elsevier B.V.
URI: https://hdl.handle.net/11499/7381
https://doi.org/10.1016/j.jpba.2014.01.012
ISSN: 0731-7085
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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