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Abstrakty
Mono- and bis-pyridinium quaternary aldoximes (K-oximes) have long been employed as cholinesterase reactivator components of antidotes against lethal cholinesterase-inhibiting organophosphorous chemicals. Their positive charge poses difficulties in their chromatographic analysis, resulting in the publication of different approaches for each K-oxime. A multiplexed method is presented for the rapid quantitation of 10 K-oximes in blood with its utility demonstrated in vivo. Liquid chromatography with absorbance detection was employed. Reversed-phase separation was achieved on a highly nonpolar stationary phase. Method validation was based on the respective guideline of the European Medicines Agency. Times to peak concentrations and 120-min areas under the time–concentration curves were determined in rats following intraperitoneal administration. Adequate retention and separation of K-oximes with acceptable peak shapes in short isocratic runs was achieved by adjusting ionic strength, organic content and the concentration of the ion-pairing agent of the mobile phase. Chromatographic properties were governed by optimizing the concentration of dissolved ions. Accurate adjustment of the organic content was indispensable for avoiding peak drifting and splitting. Dose-adjusted exposure to K-347 and K-868 was exceptionally low, while exposure to K-48 was the highest. The method is suitable for screening systemic exposure to various K-oximes and can be extended.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Strony
134--144
Opis fizyczny
Bibliogr. 28 poz., rys., tab.
Twórcy
autor
- Department of Laboratory Medicine, Semmelweis University, 4 Nagyvárad tér, Budapest, H-1089, Hungary
autor
- Department of Pharmacodynamics, Semmelweis University, 4 Nagyvárad tér, Budapest, H-1089, Hungary
autor
- Department of Pharmacology and Pharmacotherapy, Semmelweis University, 4 Nagyvárad tér, Budapest, H-1089, Hungary
autor
- Department of Laboratory Medicine, Semmelweis University, 4 Nagyvárad tér, Budapest, H-1089, Hungary
autor
- Department of Chemistry, Faculty of Science, University of Hradec Kralove, Rokitanského 62, Hradec Králové, 500 03, Czech Republic
autor
- Department of Pharmacology and Pharmacotherapy, Semmelweis University, 4 Nagyvárad tér, Budapest, H-1089, Hungary
Bibliografia
- 1. C-SS-4/DEC.3. Decision Addressing the Threat from Chemical Weapons Use; Organization for the Prohibition of Chemical Weapons: Rijswijk, 2018.
- 2. Soltaninejad, K.; Shadnia, S. In Basic and Clinical Toxicology of Organophosphorus Compounds; Balali-Mood, M.; Abdollahi, M., Eds.; Springer: Berlin, 2014; pp 25–44.
- 3. Schwartz, M. D.; Sutter, M. E.; Eisnor, D.; Kirk, M. A. Disaster Med. Public Health Prep. 2019, 13, 605.
- 4. Kassa, J.; Karasova, J.; Musilek, K.; Kuca, K. Toxicology 2008, 243, 311.
- 5. Kalász, H.; Karvaly, G.; Musilek, K.; Kuca, K.; Young-Sik, J.; Malawska, B.; Adeghate, A. A.; Nurulain, S. M.; Szepesy, J.; Zelles, T.; Tekes, K. Open Med. Chem. J. 2019, 13, 1.
- 6. Tekes, K.; Karvaly, G.; Nurulain, S.; Kuca, K.; Musilek, K.; Adeghate, E.; Jung, Y. S.; Kalász, H. Chem-Biol. Interact. 2019, 310, 108737.
- 7. National Research Council of the National Academies. Guide for the Care and Use of Laboratory Animals, 8th ed.; The National Academies Press: Washington, 2010.
- 8. R Core Team. R: A Language and Environment for Statstical Computing; R Foundation for Statistical Computing: Vienna, 2012. URL https://www.R-project.org/ (last time accessed: 15 January 2020).
- 9. Jawien, W. Pharmacokinet. Pharmacodyn. 2014, 41, 655.
- 10. Guideline on bioanalytical method validation (EMEA/CHMP/EWP/192217/2009 Rev. 1 Corr. 1**); European Medicine Agency, 2012. https://www.ema.europa.eu/documents/scientific-guideline/guideline-bioanalytical-method-validation_en.pdf. (last time accessed: 2 December 2019).
- 11. Kalász, H.; Hasan, M. Y.; Sheen, R.; Kuca, K.; Petroianu, G.; Ludányi, K.; Gergely, A.; Tekes, K. Anal. Bianal. Chem. 2006, 385, 1062.
- 12. Tekes, K.; Hasan, M. Y.; Sheen, R.; Kuca, K.; Petroianu, G.; Ludányi, K.; Kalász, H. J. Chromatogr. A 2006, 1122, 84.
- 13. Kalász, H.; Laufer, R.; Szegi, P.; Kuca, K.; Musilek, K.; Tekes, K. Acta Chromatogr. 2008, 20, 575.
- 14. Szegi, P.; Kalász, H.; Laufer, R.; Kuca, K.; Tekes, K. Anal. Bioanal. Chem. 2010, 397, 579.
- 15. Karasova, J. Z.; Hnídková, D.; Pohanka, M.; Musilek, K.; Chilcott, R. P.; Kuca, K. J. Appl. Biomed. 2012, 10, 71.
- 16. Karasova, J. Z.; Zemek, F.; Musilek, K.; Kuca, K. Neurotox. Res. 2013, 23, 63.
- 17. Zemek, F.; Karasova, J. Z.; Sepsova, V.; Kuca, K. Int. J. Mol. Sci. 2013, 14, 16076.
- 18. Lorke, D. E.; Hasan, M. Y.; Nurulain, S. M.; Sheen, R.; Kuca, K.; Petroianu, G. A. Entry of two new asymmetric bispyridinium oximes (K-27 and K-48) into the rat brain: comparison with obidoxime. J. Appl. Toxicol. 2007, 27, 482–90.
- 19. Nurulain, S. M.; Ojha, S. Dhanasekaran, S.; Kuca, K.; Nalin, N.; Sharma, C.; Adem, A.; Kalász, H. Acta Chromatogr. 2017, 29, 85..
- 20. Gyenge, M.; Kalász, H.; Petroianu, G. A.; Laufer, R.; Kuca, K.; Tekes, K. J. Chromatogr. A 2007, 1161, 146.
- 21. Kalász, H., Szegi, P., Jánoki, G., Balogh, L., Pöstényi, Z., Tekes, K. Curr. Med. Chem. 2013, 20, 2137.
- 22. Nurulain, S. M.; Kalász, H.; Kuca, K.; Adem, A.; Hasan, M. Y. B.; Hashemi, F.; Tekes, K. Acta Chromatogr. 2013, 25, 703.
- 23. Karasova, J. Z.; Kvetina, J.; Tacheci, I.; Radochova, V.; Musilek, K.; Kuca, K.; Bures, J. Toxicol. Lett. 2017, 273, 20.
- 24. Kalász, H.; Szökő, É.; Tábi, T.; Petroianu, G. A.; Lorke, D. E.; Alafifi, O. A.; Almerri, S. A.; Tekes, K. Med. Chem. 2009, 5, 237.
- 25. Lorke, D. E.; Petroianu G. A. Front. Neurosci. 2019, 13, 427.
- 26. Kassa, J.; Karasova, J.; Bajgar, J.; Kuca, K.; Musilek, K. J. Enzyme Inhib. Med. Chem. 2008, 23, 776.
- 27. Kassa, J.; Karasova, J. Z.; Kuca, K.; Musilek, K. Drug Chem. Toxicol. 2010, 33, 227.
- 28. Zorbaz, T.; Malinak, D.; Kuca, K.; Musilek, K.; Kovarik, Z. Chem-Biol. Interact. 2019, 307, 16.
Uwagi
Opracowanie rekordu ze środków MNiSW, umowa Nr 461252 w ramach programu "Społeczna odpowiedzialność nauki" - moduł: Popularyzacja nauki i promocja sportu (2021).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-353bc9ef-0f34-4518-9da6-d07198757a5f