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Abstrakty
Some new derivatives of thiosemicarbazide and the 1,2,4-triazole of sulphanylacetic acid have been chromatographed on RP-18 HPTLC plates with mobile phases containing water and an organic modifier (methanol, dioxane, acetone, 2-propanol, or tetrahydrofuran). Relationships between solute retention and modifier concentration were described by Snyder’s linear equation. The equation was used to determine R M 0 values, by extrapolation, and the S values denoting the slopes of the relationship between linear retention and mobile phase concentration; both values characterize the lipophilicity of the substances. Calculated values of R M 0 were correlated with log P values for the drugs investigated by use of the software HyperChem. Correlations between intercept ( R M 0 ) and slope ( S ) from the linear equations were also calculated. The effects of different mobile phase modifiers on experimentally obtained lipophilicity were also analysed and compared.
Czasopismo
Rocznik
Tom
Strony
37--55
Opis fizyczny
Bibliogr. 22 poz., rys., tab.
Twórcy
autor
- Medical University of Lublin Department of Inorganic Chemistry Staszica 6 20-081 Lublin Poland
autor
- Medical University of Lublin Department of Organic Chemistry Staszica 6 20-081 Lublin Poland
autor
- Medical University of Lublin Department of Organic Chemistry Staszica 6 20-081 Lublin Poland
autor
- Medical University of Lublin Department of Inorganic Chemistry Staszica 6 20-081 Lublin Poland
autor
- Medical University of Lublin Department of Inorganic Chemistry Staszica 6 20-081 Lublin Poland
Bibliografia
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- [2] F. Csizmadia, A. Tsantili-Kakoulidou, I. Panderi, and F. Darvas, J. Pharm. Sci., 86 , 865–871 (1997)
- [3] K. Jóźwiak, H. Szumiło, and E. Soczewiński, Wiad. Chem., 55 , 1047–1074 (2001) (in Polish)
- [4] E. Soczewiński and A. Wachtmeister, J. Chromatogr., 7 , 311–320 (1962)
- [5] L.R. Snyder, J.W. Dolan, and J.R. Gant, J. Chromatogr., 165 , 3 (1979)
- [6] T. DjakoviĆ-SekuliĆ, M. Ačanski, and N. Perišić-Janjić, J. Chromatogr. B, 766 , 67–75 (2001)
- [7] A. Pyka, J. Planar Chromatogr., 17 , 275–279 (2004)
- [8] J. Flieger, M. Tatarczak, M. Wujec, M. Pitucha, and H. Szumiło, J. Planar Chromatogr., 19 , 32–41 (2006)
- [9] N. Perišić-Janjić, T. Djaković-Sekulić, L. Jevrić, and B. Jovanović, J. Planar Chromatogr., 18 , 212–216 (2005)
- [10] T. Djaković-Sekulić, C. Sârbu, and N. Perišić-Janjić, J. Planar Chromatogr., 18 , 432–436 (2005)
- [11] P. Kastner, M. Kuchař, J. Klimeš, and D. Dosedlová, J. Chromatogr. A, 766 , 165–170 (1997)
- [12] J. Sochacka and A. Kowalska, J. Planar Chromatogr., 19 , 307–312 (2006)
- [13] P. Kastner, J. Klimeš, P. Velenovská, and V. Klimešová, J. Planar Chromatogr., 15 , 200–203 (2002)
- [14] J. Veličković, Ž. Tešić, and D. Milojković-Opsenica, J. Planar Chromatogr., 18 , 358–363 (2005)
- [15] HyperChem Release 8.0.6 for Windows Molecular Modeling System, V.N. Viswanadhan, A.K. Ghose, G.N. Revankar, R.K. Robins, J. Chem. Inf. Comput. Sci., 29 , 163 (1989)
- [16] N. Sadlej-Sosnowska and I. Śledzińska, J. Chromatogr., 595 , 53–61 (1992)
- [17] H.H. Jaffe, Chem. Rev., 53 , 191–196 (1953)
- [18] L.R. Snyder and J.J. Kirkland, Introduction to Modern Liquid Chromatography, Wiley, 1979, p. 286
- [19] G.L. Biagi, A.M. Barbaro, and A. Sapone, J. Chromatogr. A, 662 , 341–361 (1994)
- [20] J. Flieger, B. Modzelewska-Banachiewicz, H. Szumiło, and M. Tatarczak, Chromatographia, 60 , S291–S294 (2004)
- [21] T. Sławik and C. Kowalski, J. Chromatogr. A, 952 , 295–299 (2002)
- [22] Cs. Horváth, W. Melander, and I. Molnár, J. Chromatogr., 125 , 129 (1976)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-f5b17b1f-f754-4e82-aa2d-271c363a7a0c