Chiral separation of glycyl- and diastereomeric dipeptides and tripeptides was performed by micro-HPLC using macrocyclic antibiotics as chiral selectors. Teicoplanin was compared with teicoplanin aglycone (TAG) regarding selectivity, efficiency and separation time. The stationary phases are based on teicoplanin and TAG chemically bonded to 3.5 mum silica gel. The material was packed into 10 cm x 1 mm stainless steel microcolumns. Different mobile phases were checked using the reversed phase mode. Both teicoplanin and TAG were found to show good chiral separation ability for dipeptides. Glycyl-dipeptides were baseline resolved and most of the diastereomeric dipeptides and tripeptides were separated into their four isomers. In this study, teicoplanin was found to be advantageous compared to TAG regarding separation time, although TAG showed the higher resolution power. Baseline resolution for some glycyl-dipeptides was obtained within 3 min, diastereomeric dipeptides were resolved in 7 film. This method was also shown to be applicable for enantiomer purity control. (C) 2004 Elsevier B.V. All rights reserved.
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Inst. of Pharmaceutical Chemistry, Karl-Franzens University Graz, Universitätsplatz 1, 8010 Graz, AustriaInst. of Pharmaceutical Chemistry, Karl-Franzens University Graz, Universitätsplatz 1, 8010 Graz, Austria
Grobuschek, Nina
Schmid, Martin G.
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Inst. of Pharmaceutical Chemistry, Karl-Franzens University Graz, Universitätsplatz 1, 8010 Graz, AustriaInst. of Pharmaceutical Chemistry, Karl-Franzens University Graz, Universitätsplatz 1, 8010 Graz, Austria
Schmid, Martin G.
Koidl, Julia
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Inst. of Pharmaceutical Chemistry, Karl-Franzens University Graz, Universitätsplatz 1, 8010 Graz, AustriaInst. of Pharmaceutical Chemistry, Karl-Franzens University Graz, Universitätsplatz 1, 8010 Graz, Austria
Koidl, Julia
Gübitz, Gerald
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Inst. of Pharmaceutical Chemistry, Karl-Franzens University Graz, Universitätsplatz 1, 8010 Graz, AustriaInst. of Pharmaceutical Chemistry, Karl-Franzens University Graz, Universitätsplatz 1, 8010 Graz, Austria
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Institute of Pharmaceutical Analysis, Interdisciplinary Excellence Centre, University of Szeged, Somogyi B. u. 4, H-6720, Szeged, HungaryInstitute of Pharmaceutical Analysis, Interdisciplinary Excellence Centre, University of Szeged, Somogyi B. u. 4, H-6720, Szeged, Hungary
Tanács, Dániel
Berkecz, Róbert
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Institute of Pharmaceutical Analysis, Interdisciplinary Excellence Centre, University of Szeged, Somogyi B. u. 4, H-6720, Szeged, HungaryInstitute of Pharmaceutical Analysis, Interdisciplinary Excellence Centre, University of Szeged, Somogyi B. u. 4, H-6720, Szeged, Hungary
Berkecz, Róbert
Misicka, Aleksandra
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Department of Chemistry, University of Warsaw, Pasteura str. 1, Warsaw,02-093, PolandInstitute of Pharmaceutical Analysis, Interdisciplinary Excellence Centre, University of Szeged, Somogyi B. u. 4, H-6720, Szeged, Hungary
Misicka, Aleksandra
Tymecka, Dagmara
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Department of Chemistry, University of Warsaw, Pasteura str. 1, Warsaw,02-093, PolandInstitute of Pharmaceutical Analysis, Interdisciplinary Excellence Centre, University of Szeged, Somogyi B. u. 4, H-6720, Szeged, Hungary
Tymecka, Dagmara
Fülöp, Ferenc
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Institute of Pharmaceutical Chemistry, University of Szeged, Eötvös utca 6, H-6720, Szeged, HungaryInstitute of Pharmaceutical Analysis, Interdisciplinary Excellence Centre, University of Szeged, Somogyi B. u. 4, H-6720, Szeged, Hungary
Fülöp, Ferenc
Armstrong, Daniel W.
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Department of Chemistry and Biochemistry, University of Texas at Arlington, Arlington,TX,76019-0065, United StatesInstitute of Pharmaceutical Analysis, Interdisciplinary Excellence Centre, University of Szeged, Somogyi B. u. 4, H-6720, Szeged, Hungary
Armstrong, Daniel W.
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Ilisz, István
Péter, Antal
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Institute of Pharmaceutical Analysis, Interdisciplinary Excellence Centre, University of Szeged, Somogyi B. u. 4, H-6720, Szeged, HungaryInstitute of Pharmaceutical Analysis, Interdisciplinary Excellence Centre, University of Szeged, Somogyi B. u. 4, H-6720, Szeged, Hungary