메뉴 건너뛰기




Volumn 54, Issue 1, 2011, Pages 154-159

Generic systems for the enantioseparation of basic drugs in NACE using single-isomer anionic CDs

Author keywords

Basic drugs; In vitro metabolites; Nonaqueous capillary electrophoresis; Optimization; Single isomer anionic cyclodextrin

Indexed keywords

BUPIVACAINE; CAMPHOR; CARVEDILOL; CYCLODEXTRIN; ECONAZOLE; HEPTAKIS(2,3 DI O ACETYL 6 O SULFO)BETA CYCLODEXTRIN; HEPTAKIS(2,3 DI O METHYL 6 O SULFO)BETA CYCLODEXTRIN; ISOCONAZOLE; KETAMINE; MEPIVACAINE; METHANOL; MICONAZOLE; PRILOCAINE; SALBUTAMOL; SULCONAZOLE; TERBUTALINE; UNCLASSIFIED DRUG;

EID: 77957020306     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2010.08.004     Document Type: Article
Times cited : (26)

References (29)
  • 1
    • 77957020946 scopus 로고    scopus 로고
    • E. Francotte, W. Lindner (Eds.), Chirality in Drug Research, Methods and Principles in Medicinal Chemistry,Wiley-VCH, Weinheim
    • E. Francotte, W. Lindner (Eds.), Chirality in Drug Research, Methods and Principles in Medicinal Chemistry, vol. 33, Wiley-VCH, Weinheim, 2006.
    • (2006) , vol.33
  • 2
    • 0037096668 scopus 로고    scopus 로고
    • Chiral separations
    • Ward T. Chiral separations. Anal. Chem. 2002, 74:2863-2872.
    • (2002) Anal. Chem. , vol.74 , pp. 2863-2872
    • Ward, T.1
  • 5
    • 0034646950 scopus 로고    scopus 로고
    • Enantiomeric separations by nonaqueous capillary electrophoresis
    • Wang F., Khaledi M.G. Enantiomeric separations by nonaqueous capillary electrophoresis. J. Chromatogr. A. 2000, 875:277-293.
    • (2000) J. Chromatogr. A. , vol.875 , pp. 277-293
    • Wang, F.1    Khaledi, M.G.2
  • 6
    • 0034525270 scopus 로고    scopus 로고
    • Nonaqueous capillary electrophoresis: a versatile completion of electrophoretic separation techniques
    • Steiner F., Hassel M. Nonaqueous capillary electrophoresis: a versatile completion of electrophoretic separation techniques. Electrophoresis 2000, 21:3994-4016.
    • (2000) Electrophoresis , vol.21 , pp. 3994-4016
    • Steiner, F.1    Hassel, M.2
  • 7
    • 0034646961 scopus 로고    scopus 로고
    • Enantioselective determination by capillary electrophoresis with cyclodextrins as chiral selectors
    • Fanali S. Enantioselective determination by capillary electrophoresis with cyclodextrins as chiral selectors. J. Chromatogr. A 2000, 875:89-122.
    • (2000) J. Chromatogr. A , vol.875 , pp. 89-122
    • Fanali, S.1
  • 8
    • 0034517615 scopus 로고    scopus 로고
    • Recent progress in chiral separation principles in capillary electrophoresis
    • Gübitz G., Schmid M.G. Recent progress in chiral separation principles in capillary electrophoresis. Electrophoresis 2000, 21:4112-4135.
    • (2000) Electrophoresis , vol.21 , pp. 4112-4135
    • Gübitz, G.1    Schmid, M.G.2
  • 9
    • 0031856537 scopus 로고    scopus 로고
    • Nonaqueous capillary electrophoretic separation of enantiomers using the single-isomer heptakis(2,3-diacetyl-6-sulfo)-β-cyclodextrin as chiral resolving agent
    • Vincent J.B., Vigh G. Nonaqueous capillary electrophoretic separation of enantiomers using the single-isomer heptakis(2,3-diacetyl-6-sulfo)-β-cyclodextrin as chiral resolving agent. J. Chromatogr. A 1998, 816:233-241.
    • (1998) J. Chromatogr. A , vol.816 , pp. 233-241
    • Vincent, J.B.1    Vigh, G.2
  • 10
    • 0032429943 scopus 로고    scopus 로고
    • Capillary electrophoretic separation of weak base enantiomers using the single-isomer heptakis-(2,3-dimethyl-6-sulfato)-β-cyclodextrin as resolving agent and methanol as background electrolyte solvent
    • Cai H., Vigh G. Capillary electrophoretic separation of weak base enantiomers using the single-isomer heptakis-(2,3-dimethyl-6-sulfato)-β-cyclodextrin as resolving agent and methanol as background electrolyte solvent. J. Pharm. Biomed. Anal. 1998, 18:615-621.
    • (1998) J. Pharm. Biomed. Anal. , vol.18 , pp. 615-621
    • Cai, H.1    Vigh, G.2
  • 11
    • 0034049567 scopus 로고    scopus 로고
    • Experimental verification of a predicted, hitherto unseen separation selectivity pattern in the nonaqueous capillary electrophoretic separation of weak base enantiomers by octakis(2,3-diacetyl-6-sulfato)-γ-cyclodextrin
    • Zhu W., Vigh G. Experimental verification of a predicted, hitherto unseen separation selectivity pattern in the nonaqueous capillary electrophoretic separation of weak base enantiomers by octakis(2,3-diacetyl-6-sulfato)-γ-cyclodextrin. Electrophoresis 2000, 21:2016-2024.
    • (2000) Electrophoresis , vol.21 , pp. 2016-2024
    • Zhu, W.1    Vigh, G.2
  • 12
    • 0032860699 scopus 로고    scopus 로고
    • Nonaqueous capillary electrophoresis separation of basic enantiomers using heptakis-(2,3-dimethyl-6-sulfato)-β-cyclodextrin
    • Tacker M, Glukhovskiy P., Cai H., Vigh G. Nonaqueous capillary electrophoresis separation of basic enantiomers using heptakis-(2,3-dimethyl-6-sulfato)-β-cyclodextrin. Electrophoresis 1999, 20:2794-2798.
    • (1999) Electrophoresis , vol.20 , pp. 2794-2798
    • Tacker, M.1    Glukhovskiy, P.2    Cai, H.3    Vigh, G.4
  • 13
    • 0034665142 scopus 로고    scopus 로고
    • Enantiomer separations by nonaqueous capillary electrophoresis using octakis(2,3-diacetyl-6-sulfato)-γ-cyclodextrin
    • Zhu W., Vigh G. Enantiomer separations by nonaqueous capillary electrophoresis using octakis(2,3-diacetyl-6-sulfato)-γ-cyclodextrin. J. Chromatogr. A 2000, 892:499-507.
    • (2000) J. Chromatogr. A , vol.892 , pp. 499-507
    • Zhu, W.1    Vigh, G.2
  • 14
    • 0036192448 scopus 로고    scopus 로고
    • Nonaqueous capillary electrophoretic separation of basic enantiomers using octakis(2,3-O-dimethyl-6-O-sulfo)-gamma-cyclodextrin, a new, single-isomer chiral resolving agent
    • Busby M.B., Maldonado O., Vigh G. Nonaqueous capillary electrophoretic separation of basic enantiomers using octakis(2,3-O-dimethyl-6-O-sulfo)-gamma-cyclodextrin, a new, single-isomer chiral resolving agent. Electrophoresis 2002, 23:456-461.
    • (2002) Electrophoresis , vol.23 , pp. 456-461
    • Busby, M.B.1    Maldonado, O.2    Vigh, G.3
  • 15
    • 0037287730 scopus 로고    scopus 로고
    • Synergistic effects of ion-pairing in the enantiomeric separation of basic compounds with cyclodextrin derivatives in nonaqueous capillary electrophoresis
    • Servais A.-C., Fillet M., Abushoffa A.M., Hubert Ph., Crommen J. Synergistic effects of ion-pairing in the enantiomeric separation of basic compounds with cyclodextrin derivatives in nonaqueous capillary electrophoresis. Electrophoresis 2003, 24:363-369.
    • (2003) Electrophoresis , vol.24 , pp. 363-369
    • Servais, A.-C.1    Fillet, M.2    Abushoffa, A.M.3    Hubert, P.4    Crommen, J.5
  • 16
    • 4544365716 scopus 로고    scopus 로고
    • Enantiomeric separation of basic compounds using heptakis(2,3-di-O-methyl-6-O-sulfo)-β-cyclodextrin in combination with potassium camphorsulfonate in nonaqueous capillary electrophoresis: optimization by means of an experimental design
    • Servais A.-C., Fillet M., Chiap P., Dewé W., Ph Hubert J., Crommen Enantiomeric separation of basic compounds using heptakis(2,3-di-O-methyl-6-O-sulfo)-β-cyclodextrin in combination with potassium camphorsulfonate in nonaqueous capillary electrophoresis: optimization by means of an experimental design. Electrophoresis 2004, 25:2701-2710.
    • (2004) Electrophoresis , vol.25 , pp. 2701-2710
    • Servais, A.-C.1    Fillet, M.2    Chiap, P.3    Dewé, W.4    Ph Hubert, J.5    Crommen6
  • 17
    • 17644402814 scopus 로고    scopus 로고
    • Influence of the nature of the electrolyte on the chiral separation of basic compounds in nonaqueous capillary electrophoresis using heptakis(2,3-di-O-methyl-6-O-sulfo)-β-cyclodextrin
    • Servais A.-C., Fillet M., Chiap P., Dewé W., Hubert Ph., Crommen J. Influence of the nature of the electrolyte on the chiral separation of basic compounds in nonaqueous capillary electrophoresis using heptakis(2,3-di-O-methyl-6-O-sulfo)-β-cyclodextrin. J. Chromatogr. A 2005, 1068:143-150.
    • (2005) J. Chromatogr. A , vol.1068 , pp. 143-150
    • Servais, A.-C.1    Fillet, M.2    Chiap, P.3    Dewé, W.4    Hubert, P.5    Crommen, J.6
  • 18
    • 70450211353 scopus 로고    scopus 로고
    • Effect of the nature of the single-isomer anionic CD and the BGE composition on the enantiomeric separation of β-blockers in NACE, Electrophoresis 30
    • A. Rousseau, P. Chiap, R. Oprean, J. Crommen, M. Fillet, A.-C. Servais, Effect of the nature of the single-isomer anionic CD and the BGE composition on the enantiomeric separation of β-blockers in NACE, Electrophoresis 30 (2009) 2862-2868.
    • (2009) , pp. 2862-2868
    • Rousseau, A.1    Chiap, P.2    Oprean, R.3    Crommen, J.4    Fillet, M.5    Servais, A.-C.6
  • 19
    • 20444376522 scopus 로고    scopus 로고
    • Synthesis of heptakis(2-O-methyl-3-O-acetyl-6-O-sulfo)-cyclomaltoheptose, a single-isomer, sulfated beta-cyclodextrin carrying nonidentical substitutents at all the C2, C3, and C6 positions and its use for the capillary electrophoretic separation of enantiomers in acidic aqueous and methanolic background electrolytes
    • Busby M.B., Vigh G. Synthesis of heptakis(2-O-methyl-3-O-acetyl-6-O-sulfo)-cyclomaltoheptose, a single-isomer, sulfated beta-cyclodextrin carrying nonidentical substitutents at all the C2, C3, and C6 positions and its use for the capillary electrophoretic separation of enantiomers in acidic aqueous and methanolic background electrolytes. Electrophoresis 2005, 26:1978-1987.
    • (2005) Electrophoresis , vol.26 , pp. 1978-1987
    • Busby, M.B.1    Vigh, G.2
  • 20
    • 0018898475 scopus 로고
    • Pharmacology of ketamine isomers in surgical patients
    • White P.F, Ham J., Way W.L., Trevor A.J. Pharmacology of ketamine isomers in surgical patients. Anesthesiology 1980, 52:231-239.
    • (1980) Anesthesiology , vol.52 , pp. 231-239
    • White, P.F.1    Ham, J.2    Way, W.L.3    Trevor, A.J.4
  • 21
    • 0026638368 scopus 로고
    • Effects of ketamine on sensory perception: evidence for a role of N-methyl-d-aspartate receptors
    • Oye I., Paulsen O., Maurset A. Effects of ketamine on sensory perception: evidence for a role of N-methyl-d-aspartate receptors. J. Pharmacol. Exp. Ther. 1992, 260:1209-1213.
    • (1992) J. Pharmacol. Exp. Ther. , vol.260 , pp. 1209-1213
    • Oye, I.1    Paulsen, O.2    Maurset, A.3
  • 22
    • 0025131237 scopus 로고
    • Evidence of a role for NMDA receptors in pain perception
    • Klepstad P., Maurset A., Moberg E.R., Oye I. Evidence of a role for NMDA receptors in pain perception. Eur. J. Pharmacol. 1990, 187:513-518.
    • (1990) Eur. J. Pharmacol. , vol.187 , pp. 513-518
    • Klepstad, P.1    Maurset, A.2    Moberg, E.R.3    Oye, I.4
  • 23
    • 0037245080 scopus 로고    scopus 로고
    • Plasma concentration profiles of ketamine and norketamine after administration of various ketamine preparations to healthy Japanese volunteers
    • Yanagihara Y., Ohtani M., Kariya S., Uchino K., Hiraishi T., Ashizawa N., et al. Plasma concentration profiles of ketamine and norketamine after administration of various ketamine preparations to healthy Japanese volunteers. Biopharm. Drug Disp. 2003, 24:37-43.
    • (2003) Biopharm. Drug Disp. , vol.24 , pp. 37-43
    • Yanagihara, Y.1    Ohtani, M.2    Kariya, S.3    Uchino, K.4    Hiraishi, T.5    Ashizawa, N.6
  • 25
    • 0026491038 scopus 로고
    • Ketamin-Razemat oder S-(+)-Ketamin und Midazolam - Die Einflüsse auf Vigilanz, Leistung und subjektives Befinden
    • Doenicke A., Kugler J., Mayer M., Angster R., Hoffmann P. Ketamin-Razemat oder S-(+)-Ketamin und Midazolam - Die Einflüsse auf Vigilanz, Leistung und subjektives Befinden. Der Anaesthesist 1993, 41:610-618.
    • (1993) Der Anaesthesist , vol.41 , pp. 610-618
    • Doenicke, A.1    Kugler, J.2    Mayer, M.3    Angster, R.4    Hoffmann, P.5
  • 26
    • 0035211843 scopus 로고    scopus 로고
    • Stereoselective pharmacokinetics of ketamine: R(-)-ketamine inhibits the elimination of S(+)-ketamine
    • Ihmsen H., Geisslinger G., Schuttler J. Stereoselective pharmacokinetics of ketamine: R(-)-ketamine inhibits the elimination of S(+)-ketamine. Clin. Pharmacol. Ther. 2001, 70:431-438.
    • (2001) Clin. Pharmacol. Ther. , vol.70 , pp. 431-438
    • Ihmsen, H.1    Geisslinger, G.2    Schuttler, J.3
  • 28
    • 0019969476 scopus 로고
    • Stereochemical studies of demethylated ketamine enantiomers
    • Hong S.C., Davisson J.N. Stereochemical studies of demethylated ketamine enantiomers. J. Pharm. Sci. 1982, 71:912-914.
    • (1982) J. Pharm. Sci. , vol.71 , pp. 912-914
    • Hong, S.C.1    Davisson, J.N.2
  • 29
    • 77957019861 scopus 로고    scopus 로고
    • The European Pharmacopoeia, 6th ed., Council of Europe, Strasbourg, France
    • The European Pharmacopoeia, 6th ed., Council of Europe, Strasbourg, France, 2008.
    • (2008)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.