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Spectroscopic Analysis of Bosentan in Biological Samples After a Liquid-Liquid Microextraction Publisher



Sajediamin S1 ; Assadpourzeynali K1 ; Panahiazar V2 ; Kebriaeezadeh A3 ; Khoubnasabjafari M4 ; Ansarin K4 ; Jouybangharamaleki V5, 6 ; Jouyban A6, 7
Authors
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Authors Affiliations
  1. 1. Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, Iran
  2. 2. Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
  3. 3. Department of Pharmacoeconomics and Pharmaceutical Administration, Faculty of Pharmacy, Pharmacoeconomics and Pharmaceutical Administration Research Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Tuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
  5. 5. Department of Mechatronic Engineering, University of Tabriz, International Campus, Tabriz, Iran
  6. 6. Kimia Idea Pardaz Azarbayjan (KIPA) Science Based Company, Tabriz University of Medical Sciences, Tabriz, Iran
  7. 7. Pharmaceutical Analysis Research Center, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran

Source: BioImpacts Published:2015


Abstract

Introduction: Microextraction processes with UV-Vis measurement have been developed and validated for analysis of bosentan in biological samples. Methods: In this work, liquid-liquid microextraction procedures (DLLME & USAEME) were employed for cleanup, pre-concentration, and determination of bosentan in biological samples by UV-Vis spectroscopy at 270 nm. The method was validated and applied to the determination of bosentan in spiked serum, exhaled breath condensate and urine samples. Results: Various experimental factors including type of extraction and dispersive solvents and their volumes, pH, sonication time and centrifuging time were investigated. Under the optimum conditions, the method was linear in the range of 1.0-5.0 μg.mL-1, with coefficient of determination (R2) of < 0.998. The limit of detection (LOD) was 0.07 mg.L-1. Recovery of the target analyte in biological samples was 106.2%. The method could be easily applied for higher concentration of bosentan and needs more improvement for application in the pharmacokinetic investigations where more sensitive methods are required. Conclusion: A simple, low cost, precise and accurate spectrophotometric analysis of bosentan in biological samples after liquid-liquid microextraction were developed and validated for routine analyses. © 2015 The Author(s).
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