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Determination of vortioxetine in human serum and saliva samples by HPLC–DAD and HPLC–MS

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Vortioxetine is a new drug against major depressive disorder with high affinity for a range of different serotonergic targets in the central nervous system. Therapeutic drug monitoring is an important tool for the clinical management of patients receiving a pharmacotherapy, particularly in psychiatry. For this reason, determination of drug concentration in biological fluids is important for a rational dosage of drugs. Rapid and reliable analytical assays are also required to detect and identify drugs of toxicological importance. For analysis of vortioxetine by high-performance liquid chromatography (HPLC), no procedures for its determination in saliva have been reported and there are only a few ones for its determination in serum. A sensitive and selective highperformance liquid chromatography with diode array detector (HPLC-DAD) or mass spectrometer (HPLC-MS) method was developed for the fast quantification of vortioxetine in human saliva and serum. The determination was performed on a Synergi Polar RP column in isocratic mode under the optimal mobile phase containing 70% methanol, 20% acetate buffer at pH 3.5, 10% double distilled water, and 0.025 M L−1 diethylamine.
Słowa kluczowe
Rocznik
Strony
325--344
Opis fizyczny
Bibliogr. 14 poz.
Twórcy
  • Department of Inorganic Chemistry Medical University of Lublin, Chodźki 4a 20-093 Lublin, Poland
  • Department of Inorganic Chemistry Medical University of Lublin, Chodźki 4a 20-093 Lublin, Poland
autor
  • Department of Environmental Chemistry and Bioanalytics, Nicolaus Copernicus University, Faculty of Chemistry Gagarina 7, PL-87-100 Toruń, Poland
  • Centre for Modern Interdisciplinary Technologies, Nicolaus Copernicus University, Wileńska 4, Toruń, Poland
  • Department of Clinical Neuropsychiatry, Medical University of Lublin, Głuska 2, 20-439 Lublin, Poland
  • Department of Inorganic Chemistry Medical University of Lublin, Chodźki 4a 20-093 Lublin, Poland
Bibliografia
  • [1] L. Pehrson, S.C. Leiser, M. Gulinello, E. Dale, Y. Li, J.A. Waller, and C. Sanchez, Eur. J. Pharmacol., 753, 19 (2015)
  • [2] A. Mørk, L.P. Montezinho, S. Miller, C. Trippodi-Murphy, N. Plath, Y. Li, M. Gulinello, and C. Sanchez, Pharmacol. Biochem. Be., 105, 41 (2013)
  • [3] J.B. Jensen, K.G. Jardin, D. Song, D. Budac, G. Smagin, C. Sanchez, and A.L. Pehrsonn, Eur. Neuropsychopharma., 24, 148 (2014)
  • [4] K.A. Connors, T.W. Valenti, K. Lawless, J. Sackerman, E.S. Onaivi, B.W. Brooks, and G.G. Goulde, Aquat. Toxicol., 151, 105 (2014)
  • [5] G. Chen, R. Lee, A.-M. Højer, J.K. Buchbjerg, M. Serenko, and Z. Zhao, Clin. Drug Investig., 33, 727 (2013)
  • [6] A.L. Pehrson, T. Cremers, C. Betry, M.G.C. van der Hart, L. Jørgensena, M. Madsen, N. Haddjeri, and B. Ebert, Eur. Neuropsychopharm., 23, 133 (2013)
  • [7] C. Bétry, A. Etiévant, A. Pehrson, C. Sánchez, and N. Haddjeri, Prog. Neuro- Psychoph., 58, 38 (2015)
  • [8] H.J. Möller, Eur. Arch. Psychiatry Clin. Neurosci., 256, 476 (2006)
  • [9] P. Stenkrona, C. Halldin, and J. Lundberg, Eur. Neuropsychopharm., 23, 1190 (2013)
  • [10] G. Chen, R. Lee, A.-M. Højer, J.K. Buchbjerg, M. Serenko, and Z. Zhao, Clin. Drug Investig., 33, 727 (2013)
  • [11] E-m. Gu, C. Huang, B. Liang, L. Yuan, T. Lan, G. Hu, and H. Zhou, J. Chromatogr. B, 997, 70 (2015)
  • [12] C. Sanchez, K.E. Asin, and F. Artigas, Pharmacol. Ther., 145, 43 (2015)
  • [13] E-m. Gu, C. Huang, B. Liang, L. Yuan, T. Lan, G. Hu, and H. Zhou, J. Chromatogr. B, 997, 70–74 (2015)
  • [14] C. Sanchez, K.E. Asin, and F. Artigas, Pharmacol. Ther., 145, 43–57 (2015).
Uwagi
PL
Opracowanie ze środków MNiSW w ramach umowy 812/P-DUN/2016 na działalność upowszechniającą naukę (zadania 2017).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-ffa444c1-f922-4009-b09c-55e3fbcacb07
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