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Abstrakty
Simple and economical methods for chiral separations are always needed in synthesis and drug development and as biomarkers, besides many other useful applications. Cyclodextrins (CDs) are chiral host molecules and have been used to separate a number of chiral analytes. In this study, we have successfully prepared electrospun films of β-CD incorporated into polyvinyl alcohol (PVA) through glutaraldehyde (GA) crosslinking. These films of β-CD-PVA-GA electrospun fibers are characterized by Fourier transform infrared (FTIR) and scanning electron microscopy (SEM), which were subsequently used for thin-layer chromatography (TLC)-based enantiomeric separation of histidine and serine pairs. Amino acids were detected by spraying the chromatograms with the ninhydrin solution. Among various solvent systems employed, it was found that the separation of serine enantiomers with a resolution of 1.6 was possible with the mobile phase ethanol–butanol–ethyl acetate–water–acetone (4:5:5:0.5:1.5, v/v), and histidine enantiomers with a resolution of 1.4 were possible with the mobile phase ethanol–butanol–ethyl acetate–water–acetone (4:5:4.5:0.5:1.5, v/v). This proves that the prepared stationary phase is efficient in enatioresolution of selected amino acid pairs and can be further examined for physiological samples.
Czasopismo
Rocznik
Tom
Strony
210--213
Opis fizyczny
Bibliogr. 20 poz., rys.
Twórcy
autor
- University of Sindh, Jamshoro
autor
- University of Sindh, Jamshoro
autor
- Mehran University of Engineering and Technology, Jamshoro, Pakistan
autor
- Mehran University of Engineering and Technology, Jamshoro, Pakistan
Bibliografia
- [1] Ward, T. J.; Farris Iii, A. B. J. Chromatogr. A 2001, 906, 73.
- [2] Campbell, N.; Reece, J. Biology, San Francisco, USA, Pearson/Benjamin Cummings, 2005, p. 193.
- [3] Liu, Y.; Tian, A.; Wang, X.; Qi, J.; Wang, F.; Ma, Y.; Ito, Y.; Wei, Y. J. Chromatogr. A 2015, 1400, 40.
- [4] Miyoshi, Y.; Koga, R.; Hamase, K. D-Amino Acids, Springer, 2016, p. 3.
- [5] Paleček, E.; Ostatná, V. Electroanalysis 2007, 19, 2383.
- [6] Ilisz, I.; Berkecz, R.; Péter, A. J. Pharm. Biomed Anal. 2008, 47, 1.
- [7] Szökő, É.; Vincze, I.; Tábi, T. J. Pharm. Biomed. Anal. 2016, 130, 100.
- [8] Oyama, T.; Negishi, E.; Onigahara, H.; Kusano, N.; Miyoshi, Y.; Mita, M.; Nakazono, M.; Ohtsuki, S.; Ojida, A.; Lindner, W. J. Pharm. Biomed. Anal. 2015, 116, 71.
- [9] Nakano, Y.; Konya, Y.; Taniguchi, M.; Fukusaki, E. J. Biosci. Bioeng. 2017, 123, 134.
- [10] Fujii, N.; Takata, T.; Fujii, N.; Aki, K.; Sakaue, H. D-Amino Acids, Springer, 2016, pp. 241.
- [11] Ward, T. J.; Baker, B. A. Anal Chem. 2008, 80, 4363.
- [12] Sajewicz, M.; Piętka, R.; Pienak, A.; Kowalska, T. J Chromatogr. Sci. 2005, 43, 542.
- [13] Nagata, Y.; Iida, T.; Sakai, M. J. Mol. Catal. B. 2001, 12, 105.
- [14] Bhushan, R.; Brückner, H. Amino acids 2004, 27, 231.
- [15] Newsome, T. E.; Olesik, S. V. J. Chromatogr. A 2014, 1364, 261.
- [16] Lu, T.; Olesik, S. V. J. Chromatogr. B 2013, 912, 98.
- [17] Polak, B.; Garbacz, P. Cur. Anal. Chem. 2015, 11, 68.
- [18] Schneiderman, E.; Stalcup, A. M. J. Chromatogr. B 2000, 745, 83.
- [19] Reis, E. F. d.; Campos, F. S.; Lage, A. P.; Leite, R. C.; Heneine, L. G.; Vasconcelos, W. L.; Lobato, Z. I. P.; Mansur, H. S. Mater. Res. 2006, 9, 185.
- [20] Puguan, J. M. C.; Kim, H. Adv. Mater. Res., Trans Tech Publ, 2013, p. 1774.
Uwagi
PL
Opracowanie rekordu ze środków MNiSW, umowa Nr 461252 w ramach programu "Społeczna odpowiedzialność nauki" - moduł: Popularyzacja nauki i promocja sportu (2020).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-9b144c69-3fe4-4acf-9b0c-9b995aec028c