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Selective RP-HPLC method for determination of quetiapine in presence of coadministered drugs: Application for long-term stability study of quetiapine in whole blood

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Incidence of suicidal attempts presents an explanation for the high prevalence of quetiapine (QTI) in forensic cases. Thus, the interpretation of its concentrations in biological specimens is needed, but in forensic toxicology, potential postmortem changes such as instability of the target drugs should be taken in consideration. High-performance liquid chromatography (HPLC) method has been developed for determination of QTI. This method was based on reversed phase (RP)-HPLC separation of QTI on a C-18 column (150 mm × 4.6 mm, 5 μm) with elution system of acetonitrile—methanol—0.025 M phosphate buffer (pH 2.5), containing 1 mL TEA in each 250 mL, in a ratio of 40:30:30%, v/v, at the flow rate of 1.2 mL min−1 using mirtazapine as internal standard (IS). The proposed method was applied to the determination of QTI in plasma in presence of coadministered drugs. The application of the proposed method was extended for long-term stability study of two different concentration levels of QTI in the whole blood.
Rocznik
Strony
263--279
Opis fizyczny
Bibliogr. 24 poz., rys., tab.
Twórcy
  • Faculty of Pharmacy, Department of Pharmaceutical Analytical Chemistry, University of Alexandria, El-Messalah, Alexandria 21521, Egypt
autor
  • Faculty of Pharmacy, Department of Pharmaceutical Analytical Chemistry, University of Alexandria, El-Messalah, Alexandria 21521, Egypt
autor
  • Faculty of Pharmacy, Department of Pharmaceutical Analytical Chemistry, University of Alexandria, El-Messalah, Alexandria 21521, Egypt
autor
  • Faculty of Pharmacy, Department of Pharmaceutical Analytical Chemistry, University of Alexandria, El-Messalah, Alexandria 21521, Egypt
Bibliografia
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  • [7] J. H. Friedman, Psychoneuroendocrinology, 28 (suppl. 1), 39 (2003)
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  • [14] ICH, Q2 (R1) Validation of Analytical Procedures: Text and Methodology, International Conference on Harmonization, Geneva, 2005
  • [15] The United States Pharmacopeia and National Formulary, The Official Compendia of Standards, Asian Edition, USP 30-NF 25, Rockville, MD, 2007
  • [16] A. C. Moffat, M. D. Osselton, and B. Widdop, Clarke’s Analysis of Drugs and Poisons, 4th Ed., Pharmaceutical Press, London, UK, 2011
  • [17] R. Gieschke, Half-life. In: W. Cawello (Ed.), Parameters for Compartment-free Pharmacokinetics, Shaker, Aachen, 1999, p. 39
  • [18] P. Davis, J. Wong, and O. Gefvert, J. Pharm. Biomed. Anal., 20, 271 (1999)
  • [19] E. Saar, D. Gerostamoulos, O. Drummer, and J. Beyer, Forensic Sci. Int., 215, 152 (2011)
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Uwagi
PL
Opracowanie ze środków MNiSW w ramach umowy 812/P-DUN/2016 na działalność upowszechniającą naukę.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-45cc9491-af24-42ca-a1de-a578068fc03e
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