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Study of retention of 31 polyoxygenated steroids by normal- and reversed-phase thin-layer chromatography

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The chromatographic behavior of 31 steroidal compounds on both silica gel and RP-18 silica thin layers using nonaqueous and aqueous-organic mobile phases was investigated. It was found that an application of more polar solvent systems such as acetonitrile-dichloromethane in comparison to acetone-n-hexane resulted in stronger elution of the investigated substances in all investigated cases. Under normal-phase conditions better selectivity was achieved in acetonitrile-dichloromethane and the best in binary mixture with component ratio 1:9 (υ/υ). The selectivity of the separation under reversed-phase conditions was increased with the increased fraction of water in mobile phases used. A conclusion on the influence of substance moiety on the retention behavior of the investigated substances under reversed-phase conditions could not be drawn due to complex retention mechanism. In order to find similarities and dissimilarities between normal- and reversed-phase systems used, retention parameters were investigated by principal component analysis and cluster analysis.
Rocznik
Strony
429--445
Opis fizyczny
Bibliogr. 19 poz., rys., tab.
Twórcy
autor
  • University of Belgrade Faculty of Chemistry P.O. Box 51 11158 Belgrade Serbia
autor
  • University of Belgrade Faculty of Chemistry P.O. Box 51 11158 Belgrade Serbia
  • Central Mining Institute Department of Energy Saving and Air Protection Plac Gwarków 1 40-166
  • Central Mining Institute Department of Energy Saving and Air Protection Plac Gwarków 1 40-166 Katowice Poland
autor
  • University of Belgrade Faculty of Chemistry P.O. Box 51 11158 Belgrade Serbia
  • University of Belgrade Faculty of Chemistry P.O. Box 51 11158 Belgrade Serbia
autor
  • University of Belgrade Faculty of Chemistry P.O. Box 51 11158 Belgrade Serbia
Bibliografia
  • [1] R. Kaliszan, Quantitative Structure-Chromatographic Retention Relationships, Wiley, New York, 1987
  • [2] A.C. Duarte and S. Capelo, J. Liq. Chromatogr. Relat. Technol., 29, 1143 (2006)
  • [3] T. Joliffe, Principal Components Analysis, Springer, New York, 1986
  • [4] S. Wold, Chemom. Intell. Lab. Syst., 2, 37 (1987)
  • [5] B.G.M. Vandeginste, D.L. Massart, L.M.C. Buydens, S. De Jong, P.J. Lewi, and J. Smeyers-Verbeke, Handbook of Chemometrics and Qualimetrics: Part B, Elsevier, Amsterdam, 1998, pp. 87–150
  • [6] D.L. Massart and L. Kaufman, The Interpretation of Analytical Data by the Use of Cluster Analysis, Wiley, New York, 1983
  • [7] W. Vogt, D. Nagel, and H. Sator, Cluster Analysis in Clinical Chemistry; A Model, Wiley, New York, 1987
  • [8] L. Kaufman and P.J. Rousseeuw, Finding Groups in Data; An Introduction to Cluster Analysis, Wiley, New York, 1990
  • [9] H.C. Romesburg, Cluster Analysis for Researchers, Lifetime Learning Publications, Belmont, CA, 1984
  • [10] D. Milić, M.J. Gašić, W. Muster, J.J. Csanadi, and B.A. Šolaja, Tetrahedron, 53(41), 14073 (1997)
  • [11] D.R. Milić, T. Kop, Z. Juranić, M.J. Gašić, and B.A. Šolaja, Bioorg. Med. Chem. Lett., 11(16), 2197 (2001)
  • [12] D. Milić, T. Kop, Z. Juranić, M.J. Gašić, B. Tinant, G. Pocsfalvi, and B.A. Šolaja, Steroids, 70(14), 922 (2005)
  • [13] D. Milić, T. Kop, J. Csanadi, Z. Juranić, Z. Zizak, M.J. Gasic, and B.A. Šolaja, Steroids, 74, 890 (2009)
  • [14] A. Pyka and M. Babuska, J. Liq. Chromatogr. Relat. Technol., 29(13), 1891 (2006)
  • [15] R.P.W. Scott and P.J. Kucera, J. Chromatogr., 175, 51 (1979)
  • [16] R.M. McCormick and B.L. Karger, Anal. Chem., 52, 2249 (1980)
  • [17] A. Smoliński, B. Walczak, and J.W. Einax, Chemom. Intel. Lab. Syst., 64, 45 (2002)
  • [18] E. Van Gyseghem, S. Hemelrijck, M. Daszykowski, F. Questier, D.L. Massart, and Y. Vander Heyden, J. Chromatogr. A, 988, 77 (2003)
  • [19] F. Gritti and G. Guiochon, Anal. Chem., 77, 4257 (2005)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-5d090f34-8a60-4f2b-bd16-db97bf792119
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