메뉴 건너뛰기




Volumn 54, Issue 1-3, 2002, Pages 197-220

Stereoselective chromatography of cardiovascular drugs: An update

Author keywords

Blockers; Adrenoceptor agonists; Antiarrhythmic drugs; Calcium channel blockers; Cardiovascular drugs; Enantiomer separation

Indexed keywords

ACEBUTOLOL; ALPRENOLOL; AMLODIPINE; AROTINOLOL; ATENOLOL; BETAXOLOL; BISOPROLOL; BUCUMOLOL; BUFURALOL; BUPRANOLOL; CARBUTEROL; CARTEOLOL; CARVEDILOL; CLENBUTEROL; CLEVIDIPINE; DIPRAFENONE; DISOPYRAMIDE; FELODIPINE; FLECAINIDE; MANIDIPINE; MEXILETINE; NICARDIPINE; NIMODIPINE; NISOLDIPINE; PROPAFENONE; SALBUTAMOL; SALMETEROL; TERBUTALINE; UNINDEXED DRUG; VERAPAMIL;

EID: 0037207264     PISSN: 0165022X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-022X(02)00143-4     Document Type: Article
Times cited : (34)

References (218)
  • 2
    • 0002770991 scopus 로고
    • Stereoselectivity in adrenergic agonists and adrenergic blocking agents
    • E.J. Ariëns, W. Soudijn, & P.B.M.W.M. Timmermans. Oxford: Blackwell
    • Ruffolo R.R. Jr. Stereoselectivity in adrenergic agonists and adrenergic blocking agents. Ariëns E.J., Soudijn W., Timmermans P.B.M.W.M. Stereochemistry and biological activity of drugs. 1983;103-125 Blackwell, Oxford.
    • (1983) Stereochemistry and biological activity of drugs , pp. 103-125
    • Ruffolo R.R., Jr.1
  • 3
    • 0003452450 scopus 로고
    • The enantiomeric resolution of biologically active molecules on commercially available liquid chromatographic chiral stationary phase
    • M. Zief, & L.J. Crane. New York: Marcel Dekker
    • Wainer I.W., Alembik M.C. The enantiomeric resolution of biologically active molecules on commercially available liquid chromatographic chiral stationary phase. Zief M., Crane L.J. Chromatographic chiral separations. 1988;355-384 Marcel Dekker, New York.
    • (1988) Chromatographic chiral separations , pp. 355-384
    • Wainer, I.W.1    Alembik, M.C.2
  • 4
    • 0027487821 scopus 로고
    • The role of enantioselective liquid chromatographic separations using chiral stationary phases in pharmaceutical analysis
    • P.R. Brown, & E. Grushka. New York: Marcel Dekker
    • Levin S., Abu-Lafi S. The role of enantioselective liquid chromatographic separations using chiral stationary phases in pharmaceutical analysis. Brown P.R., Grushka E. Advances in chromatography. vol. 33:1993;233-266 Marcel Dekker, New York.
    • (1993) Advances in chromatography , vol.33 , pp. 233-266
    • Levin, S.1    Abu-Lafi, S.2
  • 5
    • 0028157517 scopus 로고
    • Progress in the separation of enantiomers of chiral drugs by HPLC without prior derivatization
    • Šubert J. Progress in the separation of enantiomers of chiral drugs by HPLC without prior derivatization. Pharmazie. 49:1994;3-13.
    • (1994) Pharmazie , vol.49 , pp. 3-13
    • Šubert, J.1
  • 6
    • 0029830246 scopus 로고    scopus 로고
    • Recent applications of chromatographic resolution of enantiomers in pharmaceutical analysis
    • Bojarski J., Aboul-Enein H.Y. Recent applications of chromatographic resolution of enantiomers in pharmaceutical analysis. Biomed. Chromatogr. 10:1996;297-302.
    • (1996) Biomed. Chromatogr. , vol.10 , pp. 297-302
    • Bojarski, J.1    Aboul-Enein, H.Y.2
  • 7
    • 0035023019 scopus 로고    scopus 로고
    • Progress in the separation of enantiomers of chiral drugs by TLC without their prior derivatization
    • Šubert J., Šlais K. Progress in the separation of enantiomers of chiral drugs by TLC without their prior derivatization. Pharmazie. 56:2001;355-360.
    • (2001) Pharmazie , vol.56 , pp. 355-360
    • Šubert, J.1    Šlais, K.2
  • 8
    • 0033058335 scopus 로고    scopus 로고
    • Recent chromatographic and electrophoretic enantioseparations of cardiovascular drugs
    • Bojarski J., Aboul-Enein H.Y. Recent chromatographic and electrophoretic enantioseparations of cardiovascular drugs. Biomed. Chromatogr. 13:1999;197-208.
    • (1999) Biomed. Chromatogr. , vol.13 , pp. 197-208
    • Bojarski, J.1    Aboul-Enein, H.Y.2
  • 9
    • 0027732756 scopus 로고
    • Enantioselective bioanalysis of beta-blocking agents: Focus on atenolol, betaxolol, carvedilol, metoprolol, pindolol, propranolol and sotalol
    • Egginger G., Lindner W., Vandenbosch C., Massart D.L. Enantioselective bioanalysis of beta-blocking agents: focus on atenolol, betaxolol, carvedilol, metoprolol, pindolol, propranolol and sotalol. Biomed. Chromatogr. 7:1993;277-295.
    • (1993) Biomed. Chromatogr. , vol.7 , pp. 277-295
    • Egginger, G.1    Lindner, W.2    Vandenbosch, C.3    Massart, D.L.4
  • 10
    • 0027314329 scopus 로고
    • Liquid chromatographic methods for the chiral separation of β-adrenergic blocking agents
    • Vandenbosch C., Massart D.L., Egginger G., Lindner W. Liquid chromatographic methods for the chiral separation of β-adrenergic blocking agents. Trends Anal. Chem. 12:1993;168-177.
    • (1993) Trends Anal. Chem. , vol.12 , pp. 168-177
    • Vandenbosch, C.1    Massart, D.L.2    Egginger, G.3    Lindner, W.4
  • 11
    • 0030965171 scopus 로고    scopus 로고
    • Synthesis of new stable aliphatic isocyanate-based chiral derivatizing agent and application to indirect separation of chiral amino and thio compounds
    • Kleidernigg O.P., Lindner W. Synthesis of new stable aliphatic isocyanate-based chiral derivatizing agent and application to indirect separation of chiral amino and thio compounds. Chromatographia. 44:1997;465-472.
    • (1997) Chromatographia , vol.44 , pp. 465-472
    • Kleidernigg, O.P.1    Lindner, W.2
  • 12
    • 0031009085 scopus 로고    scopus 로고
    • Enantioseparation of β-blockers labelled with a chiral fluorescent reagent, R(-)-DBD-PyNCS by reversed-phase liquid chromatography
    • Toyo'oka T., Toriumi M., Ishii Y. Enantioseparation of β-blockers labelled with a chiral fluorescent reagent, R(-)-DBD-PyNCS by reversed-phase liquid chromatography. J. Pharm. Biomed. Anal. 15:1997;1467-1476.
    • (1997) J. Pharm. Biomed. Anal. , vol.15 , pp. 1467-1476
    • Toyo'oka, T.1    Toriumi, M.2    Ishii, Y.3
  • 13
    • 0035111018 scopus 로고    scopus 로고
    • (R)-(-)-4-(3-isothiocyanatopyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2, 1,3-benzoxadiazole, a fluorescent chiral tagging reagent: Sensitive resolution of chiral amines and amino acids by reversed-phase liquid chromatography
    • Toyo'oka T., Jin D., Tomoi N., Oe T., Hiranuma H. (R)-(-)-4-(3-isothiocyanatopyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2, 1,3-benzoxadiazole, a fluorescent chiral tagging reagent: sensitive resolution of chiral amines and amino acids by reversed-phase liquid chromatography. Biomed. Chromatogr. 15:2001;56-67.
    • (2001) Biomed. Chromatogr. , vol.15 , pp. 56-67
    • Toyo'oka, T.1    Jin, D.2    Tomoi, N.3    Oe, T.4    Hiranuma, H.5
  • 14
    • 0033252208 scopus 로고    scopus 로고
    • Chiral separation of β-blockers after derivatization with (-)-methyl chloroformate by reversed-phase high-performance liquid chromatography
    • Kim K.H., Choi P.W., Hong S.-P., Kim H.J. Chiral separation of β-blockers after derivatization with (-)-methyl chloroformate by reversed-phase high-performance liquid chromatography. Arch. Pharm. Res. 22:1999;608-613.
    • (1999) Arch. Pharm. Res. , vol.22 , pp. 608-613
    • Kim, K.H.1    Choi, P.W.2    Hong, S.-P.3    Kim, H.J.4
  • 15
    • 0033254606 scopus 로고    scopus 로고
    • Chiral purity test of metoprolol enantiomer after derivatization with (-)-methyl chloroformate by reversed-phase high-performance liquid chromatography
    • Kim K.H., Choi P.W., Hong S.-P., Kim H.J. Chiral purity test of metoprolol enantiomer after derivatization with (-)-methyl chloroformate by reversed-phase high-performance liquid chromatography. Arch. Pharm. Res. 22:1999;614-618.
    • (1999) Arch. Pharm. Res. , vol.22 , pp. 614-618
    • Kim, K.H.1    Choi, P.W.2    Hong, S.-P.3    Kim, H.J.4
  • 16
    • 0032544730 scopus 로고    scopus 로고
    • Determination of pindolol enantiomers in human plasma and urine by simple liquid-liquid extraction and high-performance liquid chromatography
    • Beal J.L., Tett S.E. Determination of pindolol enantiomers in human plasma and urine by simple liquid-liquid extraction and high-performance liquid chromatography. J. Chromatogr. B. 715:1998;409-415.
    • (1998) J. Chromatogr. B , vol.715 , pp. 409-415
    • Beal, J.L.1    Tett, S.E.2
  • 17
    • 0034625575 scopus 로고    scopus 로고
    • Reversed-phase high-performance liquid chromatographic analysis of atenolol enantiomers in rat hepatic microsome after chiral derivatization with 2,3,4,6-tetra-O-acetyl-β-D-glycopyranosyl isothiocyanate
    • Li X., Yao T.-W., Zeng S. Reversed-phase high-performance liquid chromatographic analysis of atenolol enantiomers in rat hepatic microsome after chiral derivatization with 2,3,4,6-tetra-O-acetyl-β-D-glycopyranosyl isothiocyanate. J. Chromatogr. B. 742:2000;433-439.
    • (2000) J. Chromatogr. B , vol.742 , pp. 433-439
    • Li, X.1    Yao, T.-W.2    Zeng, S.3
  • 18
    • 0035794055 scopus 로고    scopus 로고
    • Liquid chromatographic enantioseparation of β-blocking agents with (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl isothiocyanate as chiral derivatizing agent
    • Péter M., Gyéresi A., Fülöp F. Liquid chromatographic enantioseparation of β-blocking agents with (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl isothiocyanate as chiral derivatizing agent. J. Chromatogr. A. 910:2001;247-253.
    • (2001) J. Chromatogr. A , vol.910 , pp. 247-253
    • Péter, M.1    Gyéresi, A.2    Fülöp, F.3
  • 19
    • 0032577541 scopus 로고    scopus 로고
    • Selection of internal standard for quantitative analysis of enantiomers following precolumn chiral derivatization
    • Srinivas N.R. Selection of internal standard for quantitative analysis of enantiomers following precolumn chiral derivatization. J. Chromatogr. B. 709:1998;321-323.
    • (1998) J. Chromatogr. B , vol.709 , pp. 321-323
    • Srinivas, N.R.1
  • 20
    • 0032895072 scopus 로고    scopus 로고
    • Enantioselective high performance liquid chromatographic assay of acebutolol and its active metabolite diacetolol in human serum
    • Szymura-Oleksiak J., Walczak M., Bojarski J., Aboul-Enein H.Y. Enantioselective high performance liquid chromatographic assay of acebutolol and its active metabolite diacetolol in human serum. Chirality. 11:1999;267-271.
    • (1999) Chirality , vol.11 , pp. 267-271
    • Szymura-Oleksiak, J.1    Walczak, M.2    Bojarski, J.3    Aboul-Enein, H.Y.4
  • 21
    • 0030749670 scopus 로고    scopus 로고
    • Chiral assay of atenolol present in microdialysis and plasma samples of rats using chiral CBH as stationary phase
    • Fornstedt T., Hesselgren A.-M., Johansson M. Chiral assay of atenolol present in microdialysis and plasma samples of rats using chiral CBH as stationary phase. Chirality. 9:1997;329-334.
    • (1997) Chirality , vol.9 , pp. 329-334
    • Fornstedt, T.1    Hesselgren, A.-M.2    Johansson, M.3
  • 22
    • 0034646929 scopus 로고    scopus 로고
    • Enantioselective analysis of (R)- and (S)-atenolol in urine samples by a high-performance liquid chromatography column-switching setup
    • Lamprecht G., Kraushofer T., Stoschitzky K., Lindner W. Enantioselective analysis of (R)- and (S)-atenolol in urine samples by a high-performance liquid chromatography column-switching setup. J. Chromatogr. B. 740:2000;219-226.
    • (2000) J. Chromatogr. B , vol.740 , pp. 219-226
    • Lamprecht, G.1    Kraushofer, T.2    Stoschitzky, K.3    Lindner, W.4
  • 23
    • 0343920877 scopus 로고    scopus 로고
    • Direct high-performance liquid chromatographic determination of (R)- and (S)-propranolol in rat microdialysate using on-line column switching procedures
    • Mišlanowá C., Štefancová A., Oravcová J., Horecký J., Trnovec T., Lindner W. Direct high-performance liquid chromatographic determination of (R)- and (S)-propranolol in rat microdialysate using on-line column switching procedures. J. Chromatogr. B. 739:2000;151-161.
    • (2000) J. Chromatogr. B , vol.739 , pp. 151-161
    • Mišlanowá, C.1    Štefancová, A.2    Oravcová, J.3    Horecký, J.4    Trnovec, T.5    Lindner, W.6
  • 24
    • 0031803384 scopus 로고    scopus 로고
    • Enantiomeric resolution of propranolol and analogs on two cellulose (Chiralcel OF and OC) and one amylose (Chiralpak AD) chiral stationary phases
    • Aboul-Enein H.Y., Bakr S.A. Enantiomeric resolution of propranolol and analogs on two cellulose (Chiralcel OF and OC) and one amylose (Chiralpak AD) chiral stationary phases. J. Liq. Chromatogr. Relat. Technol. 21:1998;1137-1145.
    • (1998) J. Liq. Chromatogr. Relat. Technol. , vol.21 , pp. 1137-1145
    • Aboul-Enein, H.Y.1    Bakr, S.A.2
  • 25
    • 0034657717 scopus 로고    scopus 로고
    • Evaluation of matrices containing molecularly imprinted polymers in the enantioselective-controlled delivery of β-blockers
    • Suede R., Srichana T., Martin G.P. Evaluation of matrices containing molecularly imprinted polymers in the enantioselective-controlled delivery of β-blockers. J. Control. Release. 66:2000;135-147.
    • (2000) J. Control. Release , vol.66 , pp. 135-147
    • Suede, R.1    Srichana, T.2    Martin, G.P.3
  • 27
    • 0343852119 scopus 로고    scopus 로고
    • Determination of metoprolol enantiomers in human urine by coupled achiral-chiral chromatography
    • Kim K.H., Kim H.J., Kang J.-S., Mar W. Determination of metoprolol enantiomers in human urine by coupled achiral-chiral chromatography. J. Pharm. Biomed. Anal. 22:2000;377-384.
    • (2000) J. Pharm. Biomed. Anal. , vol.22 , pp. 377-384
    • Kim, K.H.1    Kim, H.J.2    Kang, J.-S.3    Mar, W.4
  • 28
    • 0034201094 scopus 로고    scopus 로고
    • Chiral separation of enantiomers of metoprolol and its metabolites by high performance liquid chromatography
    • Kim K.H., Shin S.D., Lee J.H., Lee S.C., Kang J.S., Mar W.et al. Chiral separation of enantiomers of metoprolol and its metabolites by high performance liquid chromatography. Arch. Pharm. Res. 23:2000;230-236.
    • (2000) Arch. Pharm. Res. , vol.23 , pp. 230-236
    • Kim, K.H.1    Shin, S.D.2    Lee, J.H.3    Lee, S.C.4    Kang, J.S.5    Mar, W.6
  • 30
    • 0033955206 scopus 로고    scopus 로고
    • Enantioselective analysis of metoprolol in plasma using high-performance liquid chromatographic and indirect separations: Applications in pharmacokinetics
    • Lanchote V.L., Bonato P.S., Cerqueira P.M., Pereira V.A., Cesarino E.J. Enantioselective analysis of metoprolol in plasma using high-performance liquid chromatographic and indirect separations: applications in pharmacokinetics. J. Chromatogr. B. 738:2000;27-37.
    • (2000) J. Chromatogr. B , vol.738 , pp. 27-37
    • Lanchote, V.L.1    Bonato, P.S.2    Cerqueira, P.M.3    Pereira, V.A.4    Cesarino, E.J.5
  • 31
    • 0035879912 scopus 로고    scopus 로고
    • Enantiomeric separation of metoprolol and α-hydroxymetoprolol by liquid chromatography and fluorescence detection using a chiral stationary phase
    • Mistry B., Leslie J.L., Eddington N.D. Enantiomeric separation of metoprolol and α-hydroxymetoprolol by liquid chromatography and fluorescence detection using a chiral stationary phase. J. Chromatogr. B. 758:2001;153-161.
    • (2001) J. Chromatogr. B , vol.758 , pp. 153-161
    • Mistry, B.1    Leslie, J.L.2    Eddington, N.D.3
  • 32
    • 0032080915 scopus 로고    scopus 로고
    • Enantioselective immunoaffinity extraction for simultaneous determination of optically active bufuralol and its metabolites in human plasma by HPLC
    • Ikegawa S., Matsuura K., Sato T., Isriyanthi N.M.R., Niwa T., Miyari S.et al. Enantioselective immunoaffinity extraction for simultaneous determination of optically active bufuralol and its metabolites in human plasma by HPLC. J. Pharm. Biomed. Anal. 17:1998;1-9.
    • (1998) J. Pharm. Biomed. Anal. , vol.17 , pp. 1-9
    • Ikegawa, S.1    Matsuura, K.2    Sato, T.3    Isriyanthi, N.M.R.4    Niwa, T.5    Miyari, S.6
  • 33
    • 0030729330 scopus 로고    scopus 로고
    • Enantiomeric separation and sensitive detection of propranolol, metoprolol and atenolol derivatized with a fluorogenic reagent, 4-(N-chloroformylmethyl-N-methyl)amino-7-N,N-dimethylaminosulfonyl-2,1,3- benzoxadiazole (DBD-COCl), on cellulose chiral columns in the reversed-phase mode
    • Yang X., Fukushima T., Santa T., Homma H., Imai K. Enantiomeric separation and sensitive detection of propranolol, metoprolol and atenolol derivatized with a fluorogenic reagent, 4-(N-chloroformylmethyl-N-methyl)amino-7-N,N-dimethylaminosulfonyl-2,1,3- benzoxadiazole (DBD-COCl), on cellulose chiral columns in the reversed-phase mode. Analyst. 122:1997;1365-1369.
    • (1997) Analyst , vol.122 , pp. 1365-1369
    • Yang, X.1    Fukushima, T.2    Santa, T.3    Homma, H.4    Imai, K.5
  • 34
    • 0031578908 scopus 로고    scopus 로고
    • Sensitive chiral high-performance liquid chromatographic assay for labetalol in biological fluids
    • Dakers J.M., Boulton D.W., Fawcett J.P. Sensitive chiral high-performance liquid chromatographic assay for labetalol in biological fluids. J. Chromatogr. B. 704:1997;215-220.
    • (1997) J. Chromatogr. B , vol.704 , pp. 215-220
    • Dakers, J.M.1    Boulton, D.W.2    Fawcett, J.P.3
  • 35
    • 0031855407 scopus 로고    scopus 로고
    • Isocratic HPLC separation of several racemic drugs with two stereogenic centers on a Pirkle urea-type chiral stationary phase
    • Aboul-Enein H.Y., Al-Durabi I.A. Isocratic HPLC separation of several racemic drugs with two stereogenic centers on a Pirkle urea-type chiral stationary phase. J. Liq. Chromatogr. Relat. Technol. 21:1998;1817-1831.
    • (1998) J. Liq. Chromatogr. Relat. Technol. , vol.21 , pp. 1817-1831
    • Aboul-Enein, H.Y.1    Al-Durabi, I.A.2
  • 36
    • 0032928996 scopus 로고    scopus 로고
    • Direct separation of labetalol stereoisomers in high performance liquid chromatography system using helically self-assembled chelate as chiral selector in the mobile phase
    • Bazylak G., Aboul-Enein H.Y. Direct separation of labetalol stereoisomers in high performance liquid chromatography system using helically self-assembled chelate as chiral selector in the mobile phase. J. Liq. Chromatogr. Relat. Technol. 22:1999;1171-1192.
    • (1999) J. Liq. Chromatogr. Relat. Technol. , vol.22 , pp. 1171-1192
    • Bazylak, G.1    Aboul-Enein, H.Y.2
  • 37
    • 0033022139 scopus 로고    scopus 로고
    • Direct resolution of isamoltane (CGP 361A) and enciprazine (WY 48624) enantiomers, using chiral high performance liquid chromatography
    • Ferretti R., Gallinella B., La Torre F., Zanitti L. Direct resolution of isamoltane (CGP 361A) and enciprazine (WY 48624) enantiomers, using chiral high performance liquid chromatography. J. Liq. Chromatogr. Relat. Technol. 22:1999;1877-1892.
    • (1999) J. Liq. Chromatogr. Relat. Technol. , vol.22 , pp. 1877-1892
    • Ferretti, R.1    Gallinella, B.2    La Torre, F.3    Zanitti, L.4
  • 38
    • 0037844272 scopus 로고    scopus 로고
    • Apparent and true enantioselectivity in enantioseparations
    • Götmar G., Fornstedt T., Guiochon G. Apparent and true enantioselectivity in enantioseparations. Chirality. 12:2000;558-564.
    • (2000) Chirality , vol.12 , pp. 558-564
    • Götmar, G.1    Fornstedt, T.2    Guiochon, G.3
  • 39
    • 0035808649 scopus 로고    scopus 로고
    • Influence of the solute hydrophobicity on the enantioselective adsorption of β-blockers on a cellulase protein used as the chiral selector
    • Götmar G., Fornstedt T., Andersson M., Guiochon G. Influence of the solute hydrophobicity on the enantioselective adsorption of β-blockers on a cellulase protein used as the chiral selector. J. Chromatogr. A. 905:2001;3-17.
    • (2001) J. Chromatogr. A , vol.905 , pp. 3-17
    • Götmar, G.1    Fornstedt, T.2    Andersson, M.3    Guiochon, G.4
  • 40
    • 0035808305 scopus 로고    scopus 로고
    • Structural basis for enantiomer binding and separation of a common β-blocker: Crystal structure of cellobiohydrolase Cel7A with bound (S)-propranolol at 1.9 A resolution
    • Stahlberg J., Henriksson H., Divne C., Isaksson R., Pettersson G., Johansson G.et al. Structural basis for enantiomer binding and separation of a common β-blocker: crystal structure of cellobiohydrolase Cel7A with bound (S)-propranolol at 1.9 A resolution. J. Mol. Biol. 305:2001;79-93.
    • (2001) J. Mol. Biol. , vol.305 , pp. 79-93
    • Stahlberg, J.1    Henriksson, H.2    Divne, C.3    Isaksson, R.4    Pettersson, G.5    Johansson, G.6
  • 41
    • 0030800176 scopus 로고    scopus 로고
    • Comparison of liquid and supercritical fluid chromatography for the separation of enantiomers on chiral stationary phases
    • Williams K.L., Sander L.C., Wise S.A. Comparison of liquid and supercritical fluid chromatography for the separation of enantiomers on chiral stationary phases. J. Pharm. Biomed. Anal. 15:1997;1789-1799.
    • (1997) J. Pharm. Biomed. Anal. , vol.15 , pp. 1789-1799
    • Williams, K.L.1    Sander, L.C.2    Wise, S.A.3
  • 42
    • 0032088771 scopus 로고    scopus 로고
    • Coupled achiral/chiral column techniques in subcritical fluid chromatography for the separation of chiral and nonchiral compounds
    • Phinney K.W., Sander L.C., Wise S.A. Coupled achiral/chiral column techniques in subcritical fluid chromatography for the separation of chiral and nonchiral compounds. Anal. Chem. 70:1998;2331-2335.
    • (1998) Anal. Chem. , vol.70 , pp. 2331-2335
    • Phinney, K.W.1    Sander, L.C.2    Wise, S.A.3
  • 43
    • 0030976457 scopus 로고    scopus 로고
    • Enantiomeric separation of aromatic amino alcohol drugs by chiral ion-pair chromatography on a silica gel plate
    • Huang M.-B., Li G.-L., Yang G.-S., Shi Y.-H., Gao J.J., Liu X.-D. Enantiomeric separation of aromatic amino alcohol drugs by chiral ion-pair chromatography on a silica gel plate. J. Liq. Chromatogr. Relat. Technol. 20:1997;1507-1514.
    • (1997) J. Liq. Chromatogr. Relat. Technol. , vol.20 , pp. 1507-1514
    • Huang, M.-B.1    Li, G.-L.2    Yang, G.-S.3    Shi, Y.-H.4    Gao, J.J.5    Liu, X.-D.6
  • 44
    • 0032562428 scopus 로고    scopus 로고
    • Direct enantioseparation of some β-adrenergic blocking agents using impregnated thin-layer chromatography
    • Bushan R., Thuku Thiongo G.J. Direct enantioseparation of some β-adrenergic blocking agents using impregnated thin-layer chromatography. J. Chromatogr. B. 708:1998;330-334.
    • (1998) J. Chromatogr. B , vol.708 , pp. 330-334
    • Bushan, R.1    Thuku Thiongo, G.J.2
  • 45
    • 0034714596 scopus 로고    scopus 로고
    • Determination of the enantiomers of 3-tert-butylamino-1,2-propanediol by high-performance liquid chromatography coupled to evaporative light scattering detection
    • Toussaint B., Duchateau A.L.L., van der Wal S., Albert A., Hubert Ph., Crommen J. Determination of the enantiomers of 3-tert-butylamino-1,2-propanediol by high-performance liquid chromatography coupled to evaporative light scattering detection. J. Chromatogr. A. 890:2000;239-249.
    • (2000) J. Chromatogr. A , vol.890 , pp. 239-249
    • Toussaint, B.1    Duchateau, A.L.L.2    Van der Wal, S.3    Albert, A.4    Hubert, Ph.5    Crommen, J.6
  • 46
    • 0034721970 scopus 로고    scopus 로고
    • Determination of the enantiomers of 3-tert-butylamino-1,2-propanediol by high-performance liquid chromatography using mass spectrometric detection
    • Toussaint B., Streel B., Ceccato A., Hubert Ph., Crommen J. Determination of the enantiomers of 3-tert-butylamino-1,2-propanediol by high-performance liquid chromatography using mass spectrometric detection. J. Chromatogr. A. 896:2000;201-207.
    • (2000) J. Chromatogr. A , vol.896 , pp. 201-207
    • Toussaint, B.1    Streel, B.2    Ceccato, A.3    Hubert, Ph.4    Crommen, J.5
  • 47
    • 0032035155 scopus 로고    scopus 로고
    • Coupled chiral chromatography in chiral separation of salmeterol
    • Kim K.H., Yun H.W., Kim H.J., Park H.J., Choi P.W. Coupled chiral chromatography in chiral separation of salmeterol. Arch. Pharm. Res. 21:1998;212-216.
    • (1998) Arch. Pharm. Res. , vol.21 , pp. 212-216
    • Kim, K.H.1    Yun, H.W.2    Kim, H.J.3    Park, H.J.4    Choi, P.W.5
  • 48
    • 0032035394 scopus 로고    scopus 로고
    • Resolution of salbutamol enantiomers in human urine by reversed-phase high-performance liquid chromatography after derivatization with 2,3,4,6-tetra-O-acetyl-β-D-glucopyranose isothiocyanate
    • Kim K.H., Kim T.K. Resolution of salbutamol enantiomers in human urine by reversed-phase high-performance liquid chromatography after derivatization with 2,3,4,6-tetra-O-acetyl-β-D-glucopyranose isothiocyanate. Arch. Pharm. Res. 21:1998;217-222.
    • (1998) Arch. Pharm. Res. , vol.21 , pp. 217-222
    • Kim, K.H.1    Kim, T.K.2
  • 49
    • 0032977029 scopus 로고    scopus 로고
    • Analytical methodology for enantiomers of salbutamol in human urine for application in doping control
    • Bergés R., Segura J., de la Torre X., Ventura R. Analytical methodology for enantiomers of salbutamol in human urine for application in doping control. J. Chromatogr. B. 723:1999;173-184.
    • (1999) J. Chromatogr. B , vol.723 , pp. 173-184
    • Bergés, R.1    Segura, J.2    De la Torre, X.3    Ventura, R.4
  • 50
    • 0031857156 scopus 로고    scopus 로고
    • Determination of the enantiomers of albuterol in human and canine plasma by enantioselective high-performance liquid chromatography on a teicoplanin-based chiral stationary phase
    • Fried K.M., Koch P., Wainer I.W. Determination of the enantiomers of albuterol in human and canine plasma by enantioselective high-performance liquid chromatography on a teicoplanin-based chiral stationary phase. Chirality. 10:1998;484-491.
    • (1998) Chirality , vol.10 , pp. 484-491
    • Fried, K.M.1    Koch, P.2    Wainer, I.W.3
  • 51
    • 0032903993 scopus 로고    scopus 로고
    • In situ arrangement of supramolecules throughout direct separation of carbuterol enantiomers in RP-HPLC system with helical additives in mobile phase
    • Bazylak G., Aboul-Enein H.Y. In situ arrangement of supramolecules throughout direct separation of carbuterol enantiomers in RP-HPLC system with helical additives in mobile phase. Anal. Lett. 32:1999;521-551.
    • (1999) Anal. Lett. , vol.32 , pp. 521-551
    • Bazylak, G.1    Aboul-Enein, H.Y.2
  • 52
    • 0033040003 scopus 로고    scopus 로고
    • Supramolecular effects in chiral discrimination of clenbuterol enantiomers in RP-HPLC system with helically self-assembled mobile-phase additive. Retention studies and molecular modeling approach
    • Bazylak G., Aboul-Enein H.Y. Supramolecular effects in chiral discrimination of clenbuterol enantiomers in RP-HPLC system with helically self-assembled mobile-phase additive. Retention studies and molecular modeling approach. Chirality. 11:1999;387-393.
    • (1999) Chirality , vol.11 , pp. 387-393
    • Bazylak, G.1    Aboul-Enein, H.Y.2
  • 53
    • 0034527183 scopus 로고    scopus 로고
    • Stereochemical composition of clenbuterol residues in edible tissues of swine
    • Smith D.J. Stereochemical composition of clenbuterol residues in edible tissues of swine. J. Agric. Food Chem. 48:2000;6036-6043.
    • (2000) J. Agric. Food Chem. , vol.48 , pp. 6036-6043
    • Smith, D.J.1
  • 54
    • 0032860855 scopus 로고    scopus 로고
    • Optimized enantioselective separation of clenbuterol on macrocyclic antibiotic teicoplanin chiral stationary phase
    • Aboul-Enein H.Y., Serignese V. Optimized enantioselective separation of clenbuterol on macrocyclic antibiotic teicoplanin chiral stationary phase. J. Liq. Chromatogr. Relat. Technol. 22:1999;2177-2185.
    • (1999) J. Liq. Chromatogr. Relat. Technol. , vol.22 , pp. 2177-2185
    • Aboul-Enein, H.Y.1    Serignese, V.2
  • 55
    • 0033371422 scopus 로고    scopus 로고
    • Quantitative determination of clenbuterol enantiomers in human plasma by high-performance liquid chromatography using the macrocyclic antibiotic chiral stationary phase teicoplanin
    • Aboul-Enein H.Y., Serignese V. Quantitative determination of clenbuterol enantiomers in human plasma by high-performance liquid chromatography using the macrocyclic antibiotic chiral stationary phase teicoplanin. Biomed. Chromatogr. 13:1999;520-524.
    • (1999) Biomed. Chromatogr. , vol.13 , pp. 520-524
    • Aboul-Enein, H.Y.1    Serignese, V.2
  • 56
    • 0034137706 scopus 로고    scopus 로고
    • Reversed-phase high performance liquid chromatographic separations of the enantiomers of terbutaline by derivatization with 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate
    • Kim K.H., Kim D.S., Hong S.-P., Keon O.S. Reversed-phase high performance liquid chromatographic separations of the enantiomers of terbutaline by derivatization with 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate. Arch. Pharm. Res. 23:2000;26-30.
    • (2000) Arch. Pharm. Res. , vol.23 , pp. 26-30
    • Kim, K.H.1    Kim, D.S.2    Hong, S.-P.3    Keon, O.S.4
  • 58
    • 0035085769 scopus 로고    scopus 로고
    • High-performance liquid chromatographic and capillary electrophoretic methods for the quantitation of the (S)-terbutaline in (R)-terbutaline
    • Kim K.H., Kim H.J., Kim J.H., Lee J.H., Lee S.C. High-performance liquid chromatographic and capillary electrophoretic methods for the quantitation of the (S)-terbutaline in (R)-terbutaline. Chromatographia. 53:2001;334-337.
    • (2001) Chromatographia , vol.53 , pp. 334-337
    • Kim, K.H.1    Kim, H.J.2    Kim, J.H.3    Lee, J.H.4    Lee, S.C.5
  • 59
    • 0035835410 scopus 로고    scopus 로고
    • Determination of terbutaline enantiomers in human urine by coupled achiral-chiral high-performance liquid chromatography with fluorescence detection
    • Kim K.H., Kim H.J., Kim J.-H., Shin S.D. Determination of terbutaline enantiomers in human urine by coupled achiral-chiral high-performance liquid chromatography with fluorescence detection. J. Chromatogr. B. 751:2001;69-77.
    • (2001) J. Chromatogr. B , vol.751 , pp. 69-77
    • Kim, K.H.1    Kim, H.J.2    Kim, J.-H.3    Shin, S.D.4
  • 60
    • 0031444026 scopus 로고    scopus 로고
    • Enantioselective determination of the hydroxylated metabolites of mexiletine in human plasma
    • Lanchote V.L., Bonato P.S., Cesarino E.J., Mere Y.A. Jr., Cavani S.R., Santos J.et al. Enantioselective determination of the hydroxylated metabolites of mexiletine in human plasma. Chirality. 9:1997;732-738.
    • (1997) Chirality , vol.9 , pp. 732-738
    • Lanchote, V.L.1    Bonato, P.S.2    Cesarino, E.J.3    Mere Y.A., Jr.4    Cavani, S.R.5    Santos, J.6
  • 61
    • 0031046823 scopus 로고    scopus 로고
    • Enantioselective determination of diprafenone in human plasma
    • Zhong D., Chen R., Fieger-Büschges H., Blume H. Enantioselective determination of diprafenone in human plasma. Pharmazie. 52:1997;106-109.
    • (1997) Pharmazie , vol.52 , pp. 106-109
    • Zhong, D.1    Chen, R.2    Fieger-Büschges, H.3    Blume, H.4
  • 62
    • 0033728594 scopus 로고    scopus 로고
    • Stereoselective determination of propafenone enantiomers in transgenic Chinese hamster CHL cells expressing human cytochrome P450
    • Yao T.W., Zhou Q., Zeng S. Stereoselective determination of propafenone enantiomers in transgenic Chinese hamster CHL cells expressing human cytochrome P450. Biomed. Chromatogr. 14:2000;498-501.
    • (2000) Biomed. Chromatogr. , vol.14 , pp. 498-501
    • Yao, T.W.1    Zhou, Q.2    Zeng, S.3
  • 63
    • 0032562408 scopus 로고    scopus 로고
    • Enantioselective analysis of propafenone in plasma using a polysaccharide-based chiral stationary phase under reversed-phase conditions
    • de Gaitani C.M., Lanchote V.L., Bonato P.S. Enantioselective analysis of propafenone in plasma using a polysaccharide-based chiral stationary phase under reversed-phase conditions. J. Chromatogr. B. 708:1998;177-183.
    • (1998) J. Chromatogr. B , vol.708 , pp. 177-183
    • De Gaitani, C.M.1    Lanchote, V.L.2    Bonato, P.S.3
  • 64
    • 0032907317 scopus 로고    scopus 로고
    • Enantioselective determination of propafenone and its metabolites in human plasma by liquid chromatography-mass spectrometry
    • Zhong D., Chen X. Enantioselective determination of propafenone and its metabolites in human plasma by liquid chromatography-mass spectrometry. J. Chromatogr. B. 721:1999;67-75.
    • (1999) J. Chromatogr. B , vol.721 , pp. 67-75
    • Zhong, D.1    Chen, X.2
  • 65
    • 0033005362 scopus 로고    scopus 로고
    • Simultaneous determination of propafenone and 5-hydroxypropafenone enantiomers in plasma by chromatography on an amylose derived stationary phase
    • de Abreu L.R.P., Lanchote V.L., Bertucci C., Cesarino E.J., Bonato P.S. Simultaneous determination of propafenone and 5-hydroxypropafenone enantiomers in plasma by chromatography on an amylose derived stationary phase. J. Pharm. Biomed. Anal. 20:1999;209-216.
    • (1999) J. Pharm. Biomed. Anal. , vol.20 , pp. 209-216
    • De Abreu, L.R.P.1    Lanchote, V.L.2    Bertucci, C.3    Cesarino, E.J.4    Bonato, P.S.5
  • 66
    • 0034090032 scopus 로고    scopus 로고
    • Enantioselective HPLC analysis of propafenone and of its main metabolites using polysaccharide and protein based chiral stationary phases
    • Bonato P.S., de Abreu L.R.P., de Gaitani C.M., Lanchote V.L., Bertucci C. Enantioselective HPLC analysis of propafenone and of its main metabolites using polysaccharide and protein based chiral stationary phases. Biomed. Chromatogr. 14:2000;227-233.
    • (2000) Biomed. Chromatogr. , vol.14 , pp. 227-233
    • Bonato, P.S.1    De Abreu, L.R.P.2    De Gaitani, C.M.3    Lanchote, V.L.4    Bertucci, C.5
  • 67
    • 0034698345 scopus 로고    scopus 로고
    • Enantioselective analysis of disopyramide and N-monodealkyldisopyramide in plasma and urine by high-performance liquid chromatography on an amylose-derived chiral stationary phase
    • Bortocan R., Lanchote V.L., Cesarino E.J., Bonato P.S. Enantioselective analysis of disopyramide and N-monodealkyldisopyramide in plasma and urine by high-performance liquid chromatography on an amylose-derived chiral stationary phase. J. Chromatogr. B. 744:2000;299-306.
    • (2000) J. Chromatogr. B , vol.744 , pp. 299-306
    • Bortocan, R.1    Lanchote, V.L.2    Cesarino, E.J.3    Bonato, P.S.4
  • 68
    • 0033023089 scopus 로고    scopus 로고
    • Chiral stationary phases based on cellulose and amylose tris-3,5-dimethylphenylcarbamate derivatives for the resolution of selected chiral drugs and metabolites
    • Bonato P.S., Lanchote V.L., Bortocan R., Jabor V.A.P., Paias F.O., Ricci-Júnior E.et al. Chiral stationary phases based on cellulose and amylose tris-3,5-dimethylphenylcarbamate derivatives for the resolution of selected chiral drugs and metabolites. J. Liq. Chromatogr. Relat. Technol. 22:1999;1813-1827.
    • (1999) J. Liq. Chromatogr. Relat. Technol. , vol.22 , pp. 1813-1827
    • Bonato, P.S.1    Lanchote, V.L.2    Bortocan, R.3    Jabor, V.A.P.4    Paias, F.O.5    Ricci-Júnior, E.6
  • 69
    • 0032511239 scopus 로고    scopus 로고
    • Quantitative determination of disopyramide, verapamil and flecainide enantiomers in rat plasma and tissues by high-performance liquid chromatography
    • Hanada K., Akimoto S., Mitsui K., Hashiguchi M., Ogata H. Quantitative determination of disopyramide, verapamil and flecainide enantiomers in rat plasma and tissues by high-performance liquid chromatography. J. Chromatogr. B. 710:1998;129-135.
    • (1998) J. Chromatogr. B , vol.710 , pp. 129-135
    • Hanada, K.1    Akimoto, S.2    Mitsui, K.3    Hashiguchi, M.4    Ogata, H.5
  • 70
    • 0031005937 scopus 로고    scopus 로고
    • Resolution of the enantiomers of verapamil and gallopamil by chiral liquid chromatography-mass spectrometry
    • Rustichelli C., Ferioli V., Gamberini G. Resolution of the enantiomers of verapamil and gallopamil by chiral liquid chromatography-mass spectrometry. Chromatographia. 44:1997;477-483.
    • (1997) Chromatographia , vol.44 , pp. 477-483
    • Rustichelli, C.1    Ferioli, V.2    Gamberini, G.3
  • 71
    • 0032585784 scopus 로고    scopus 로고
    • Enantiomeric separation of verapamil and norverapamil using Chiral-AGP® as the stationary phase
    • Sandström R., Lennernäs H., Öhlén K., Karlsson A. Enantiomeric separation of verapamil and norverapamil using Chiral-AGP® as the stationary phase. J. Pharm. Biomed. Anal. 21:1999;43-49.
    • (1999) J. Pharm. Biomed. Anal. , vol.21 , pp. 43-49
    • Sandström, R.1    Lennernäs, H.2    Öhlén, K.3    Karlsson, A.4
  • 72
    • 0032503055 scopus 로고    scopus 로고
    • Solid-phase extraction-high-performance liquid chromatography determination of verapamil and norverapamil enantiomers in urine
    • Asafu-Adjaye E.B., Shiu G.K. Solid-phase extraction-high-performance liquid chromatography determination of verapamil and norverapamil enantiomers in urine. J. Chromatogr. B. 707:1998;161-167.
    • (1998) J. Chromatogr. B , vol.707 , pp. 161-167
    • Asafu-Adjaye, E.B.1    Shiu, G.K.2
  • 73
    • 0345425617 scopus 로고    scopus 로고
    • Achiral and chiral high-performance liquid chromatography of verapamil and its metabolites in serum samples
    • Brandšteterova E., Wainer I.W. Achiral and chiral high-performance liquid chromatography of verapamil and its metabolites in serum samples. J. Chromatogr. B. 732:1999;395-404.
    • (1999) J. Chromatogr. B , vol.732 , pp. 395-404
    • Brandšteterova, E.1    Wainer, I.W.2
  • 74
    • 0034099682 scopus 로고    scopus 로고
    • Simultaneous HPLC analysis of S- and R-verapamil and metabolites, S- and R-norverapamil in human plasma
    • Ho P.C., Saville D.J., Wanwimolruk S. Simultaneous HPLC analysis of S- and R-verapamil and metabolites, S- and R-norverapamil in human plasma. J. Liq. Chromatogr. Relat. Technol. 23:2000;1711-1723.
    • (2000) J. Liq. Chromatogr. Relat. Technol. , vol.23 , pp. 1711-1723
    • Ho, P.C.1    Saville, D.J.2    Wanwimolruk, S.3
  • 75
    • 0344562905 scopus 로고    scopus 로고
    • Achiral and chiral HPLC analysis of norverapamil and its metabolites in microsomal samples
    • Brandšteterova E., Wainer I.W., Tracy T. Achiral and chiral HPLC analysis of norverapamil and its metabolites in microsomal samples. Neoplasma. 46:1999;207-211.
    • (1999) Neoplasma , vol.46 , pp. 207-211
    • Brandšteterova, E.1    Wainer, I.W.2    Tracy, T.3
  • 76
    • 0031557187 scopus 로고    scopus 로고
    • Column-switching techniques in the biomedical analysis of stereoisomeric drugs: Why, how and when
    • Fried K., Wainer I.W. Column-switching techniques in the biomedical analysis of stereoisomeric drugs: why, how and when. J. Chromatogr. B. 689:1997;91-104.
    • (1997) J. Chromatogr. B , vol.689 , pp. 91-104
    • Fried, K.1    Wainer, I.W.2
  • 77
    • 0028918956 scopus 로고
    • Stereoselective pharmacokinetics of dihydropyridine calcium antagonists
    • Tokuma Y., Noguchi H. Stereoselective pharmacokinetics of dihydropyridine calcium antagonists. J. Chromatogr. A. 694:1995;181-193.
    • (1995) J. Chromatogr. A , vol.694 , pp. 181-193
    • Tokuma, Y.1    Noguchi, H.2
  • 78
    • 0030765857 scopus 로고    scopus 로고
    • Enantioselective high-performance liquid chromatographic determination of nicardipine in human plasma
    • Uno T., Ohkubo T., Sugawara K. Enantioselective high-performance liquid chromatographic determination of nicardipine in human plasma. J. Chromatogr. B. 698:1997;181-186.
    • (1997) J. Chromatogr. B , vol.698 , pp. 181-186
    • Uno, T.1    Ohkubo, T.2    Sugawara, K.3
  • 79
    • 0032928995 scopus 로고    scopus 로고
    • Enantioselective high-performance liquid chromatographic determination of manidipine in human plasma
    • Uno T., Ohkubo T., Sugawara K. Enantioselective high-performance liquid chromatographic determination of manidipine in human plasma. J. Liq. Chromatogr. Relat. Technol. 22:1999;1117-1128.
    • (1999) J. Liq. Chromatogr. Relat. Technol. , vol.22 , pp. 1117-1128
    • Uno, T.1    Ohkubo, T.2    Sugawara, K.3
  • 80
    • 0032570919 scopus 로고    scopus 로고
    • Effect of charged and uncharged chiral additives on the resolution of amlodipine enantiomers in liquid chromatography and capillary electrophoresis
    • Owens P.K., Fell A.F., Coleman M.W., Berridge J.C. Effect of charged and uncharged chiral additives on the resolution of amlodipine enantiomers in liquid chromatography and capillary electrophoresis. J. Chromatogr. A. 797:1998;187-195.
    • (1998) J. Chromatogr. A , vol.797 , pp. 187-195
    • Owens, P.K.1    Fell, A.F.2    Coleman, M.W.3    Berridge, J.C.4
  • 81
    • 0030957177 scopus 로고    scopus 로고
    • Semi-preparative chromatographic purification of the enantiomers of S-(-) amlodipine and R-(+) amlodipine
    • Lukša J., Josic D., Podobnik B., Furlan M., Kremser J. Semi-preparative chromatographic purification of the enantiomers of S-(-) amlodipine and R-(+) amlodipine. J. Chromatogr. B. 639:1997;367-375.
    • (1997) J. Chromatogr. B , vol.639 , pp. 367-375
    • Lukša, J.1    Josic, D.2    Podobnik, B.3    Furlan, M.4    Kremser, J.5
  • 82
    • 0031450345 scopus 로고    scopus 로고
    • Pharmacokinetic behaviour of R-(+)- and S-(-)-amlodipine after single enantiomer administration
    • Lukša J., Josic D., Kremser J., Kopitar Z., Milutinovic S. Pharmacokinetic behaviour of R-(+)- and S-(-)-amlodipine after single enantiomer administration. J. Chromatogr. B. 703:1997;185-193.
    • (1997) J. Chromatogr. B , vol.703 , pp. 185-193
    • Lukša, J.1    Josic, D.2    Kremser, J.3    Kopitar, Z.4    Milutinovic, S.5
  • 83
    • 0035111455 scopus 로고    scopus 로고
    • Enantioselective pharmacokinetics of the enantiomers of clevidipine following intravenous infusion of the racemate in essential hypertensive patients
    • Ericsson H., Schwieler J., Lindmark B., Löfdahl P., Thulin T., Regardh C.G. Enantioselective pharmacokinetics of the enantiomers of clevidipine following intravenous infusion of the racemate in essential hypertensive patients. Chirality. 13:2001;130-134.
    • (2001) Chirality , vol.13 , pp. 130-134
    • Ericsson, H.1    Schwieler, J.2    Lindmark, B.3    Löfdahl, P.4    Thulin, T.5    Regardh, C.G.6
  • 84
    • 0033830771 scopus 로고    scopus 로고
    • Enantioresolution of dihydropyridine substituted acid by supercritical fluid chromatography on Hypercarb® with Z-(L)-arginine as chiral counter ion
    • Gyllenhaal O., Karlsson A. Enantioresolution of dihydropyridine substituted acid by supercritical fluid chromatography on Hypercarb® with Z-(L)-arginine as chiral counter ion. Chromatographia. 52:2000;351-355.
    • (2000) Chromatographia , vol.52 , pp. 351-355
    • Gyllenhaal, O.1    Karlsson, A.2
  • 85
    • 0035114655 scopus 로고    scopus 로고
    • Addition of organic modifiers to control retention order of enantiomers of dihydropyridines on chiral-AGP
    • Karlsson A., Nyström A. Addition of organic modifiers to control retention order of enantiomers of dihydropyridines on chiral-AGP. Chromatographia. 53:2001;135-139.
    • (2001) Chromatographia , vol.53 , pp. 135-139
    • Karlsson, A.1    Nyström, A.2
  • 86
    • 0035812962 scopus 로고    scopus 로고
    • Enantioselective assay of nisoldipine in human plasma by chiral high-performance liquid chromatography combined with gas-chromatographic-mass spectrometry: Applications to pharmacokinetics
    • Marques M.P., Santos N.A.G., Coelho E.B., Bonato P.S., Lanchote V.L. Enantioselective assay of nisoldipine in human plasma by chiral high-performance liquid chromatography combined with gas-chromatographic-mass spectrometry: applications to pharmacokinetics. J. Chromatogr. B. 762:2001;87-95.
    • (2001) J. Chromatogr. B , vol.762 , pp. 87-95
    • Marques, M.P.1    Santos, N.A.G.2    Coelho, E.B.3    Bonato, P.S.4    Lanchote, V.L.5
  • 87
    • 0031790886 scopus 로고    scopus 로고
    • Enantioselective determination of isradipine in human serum using chiral stationary phase liquid chromatography and gas chromatography with nitrogen selective detection
    • Rask H., Angelo H.R., Christensen H.R. Enantioselective determination of isradipine in human serum using chiral stationary phase liquid chromatography and gas chromatography with nitrogen selective detection. Chirality. 10:1998;808-812.
    • (1998) Chirality , vol.10 , pp. 808-812
    • Rask, H.1    Angelo, H.R.2    Christensen, H.R.3
  • 88
    • 0035097470 scopus 로고    scopus 로고
    • Normal-phase TLC separation of enantiomers of 1,4-dihydropyrimidine derivatives
    • Mielcarek J. Normal-phase TLC separation of enantiomers of 1,4-dihydropyrimidine derivatives. Drug Dev. Ind. Pharm. 27:2001;175-179.
    • (2001) Drug Dev. Ind. Pharm. , vol.27 , pp. 175-179
    • Mielcarek, J.1
  • 89
    • 0030780507 scopus 로고    scopus 로고
    • Chiral resolution of four optical isomers of diltiazem hydrochloride on Chiralcel columns by packed-column supercritical fluid chromatography
    • Yaku K., Aoe K., Nishimura N., Sato T., Morishita F. Chiral resolution of four optical isomers of diltiazem hydrochloride on Chiralcel columns by packed-column supercritical fluid chromatography. J. Chromatogr. A. 785:1997;185-193.
    • (1997) J. Chromatogr. A , vol.785 , pp. 185-193
    • Yaku, K.1    Aoe, K.2    Nishimura, N.3    Sato, T.4    Morishita, F.5
  • 90
    • 77954738458 scopus 로고    scopus 로고
    • Direct chiral resolution of optical isomers of diltiazem hydrochloride by packed column supercritical fluid chromatography
    • J.R. Williams, & A.A. Clifford. Totowa, NJ: Humana Press
    • Yaku K., Aoe K., Nishimura N., Sato T., Morishita F. Direct chiral resolution of optical isomers of diltiazem hydrochloride by packed column supercritical fluid chromatography. Williams J.R., Clifford A.A. Supercritical fluid methods and protocols. 2000;149-156 Humana Press, Totowa, NJ.
    • (2000) Supercritical fluid methods and protocols , pp. 149-156
    • Yaku, K.1    Aoe, K.2    Nishimura, N.3    Sato, T.4    Morishita, F.5
  • 91
    • 0030923143 scopus 로고    scopus 로고
    • Enantioselective protein binding of semotiadil and levosemotiadil determined by high-performance frontal analysis
    • Rodriguez Rosas M.E., Shibukawa A., Ueda K., Nakagawa T. Enantioselective protein binding of semotiadil and levosemotiadil determined by high-performance frontal analysis. J. Pharm. Biomed. Anal. 15:1997;1595-1601.
    • (1997) J. Pharm. Biomed. Anal. , vol.15 , pp. 1595-1601
    • Rodriguez Rosas, M.E.1    Shibukawa, A.2    Ueda, K.3    Nakagawa, T.4
  • 93
    • 0033005140 scopus 로고    scopus 로고
    • Analytical resolution of 4-aryl-1,2,3,4,5,6,7,8-octahydroquinazoline-2-thiones using a cellulose chiral stationary phase
    • Saraç S., Yarym M., Ertan M. Analytical resolution of 4-aryl-1,2,3,4,5,6,7,8-octahydroquinazoline-2-thiones using a cellulose chiral stationary phase. Anal. Lett. 32:1999;1245-1254.
    • (1999) Anal. Lett. , vol.32 , pp. 1245-1254
    • Saraç, S.1    Yarym, M.2    Ertan, M.3
  • 94
    • 0030826062 scopus 로고    scopus 로고
    • Determination of unbound warfarin enantiomers in human plasma and 7-hydroxywarfarin in human urine by chiral stationary-phase liquid chromatography with ultraviolet detection or fluorescence and on-line circular dichroism detection
    • Takahashi H., Kashima T., Kimura S., Muramoto N., Nakahata H., Kubo S.et al. Determination of unbound warfarin enantiomers in human plasma and 7-hydroxywarfarin in human urine by chiral stationary-phase liquid chromatography with ultraviolet detection or fluorescence and on-line circular dichroism detection. J. Chromatogr. B. 701:1997;71-80.
    • (1997) J. Chromatogr. B , vol.701 , pp. 71-80
    • Takahashi, H.1    Kashima, T.2    Kimura, S.3    Muramoto, N.4    Nakahata, H.5    Kubo, S.6
  • 95
    • 0032511212 scopus 로고    scopus 로고
    • Chiral phase analysis of warfarin enantiomers in patient plasma in relation to CYP2C9 genotype
    • Henne K.R., Gaedigk A., Gupta G., Leeder J.S., Rettie A.E. Chiral phase analysis of warfarin enantiomers in patient plasma in relation to CYP2C9 genotype. J. Chromatogr. B. 710:1998;143-148.
    • (1998) J. Chromatogr. B , vol.710 , pp. 143-148
    • Henne, K.R.1    Gaedigk, A.2    Gupta, G.3    Leeder, J.S.4    Rettie, A.E.5
  • 96
    • 0032032321 scopus 로고    scopus 로고
    • Chiral bioanalysis of warfarin using microbore LC with peak compression
    • Prangle A.S., Noctor T.A.G., Lough W.J. Chiral bioanalysis of warfarin using microbore LC with peak compression. J. Pharm. Biomed. Anal. 16:1998;1205-1212.
    • (1998) J. Pharm. Biomed. Anal. , vol.16 , pp. 1205-1212
    • Prangle, A.S.1    Noctor, T.A.G.2    Lough, W.J.3
  • 97
    • 0034112062 scopus 로고    scopus 로고
    • Validation of a method for the determination of (R)-warfarin and (S)-warfarin in human plasma using LC with UV detection
    • Ring P.R., Bostick J.M. Validation of a method for the determination of (R)-warfarin and (S)-warfarin in human plasma using LC with UV detection. J. Pharm. Biomed. Anal. 22:2000;573-581.
    • (2000) J. Pharm. Biomed. Anal. , vol.22 , pp. 573-581
    • Ring, P.R.1    Bostick, J.M.2
  • 98
    • 0035078166 scopus 로고    scopus 로고
    • Development and validation of a sensitive and robust LC-tandem MS method for the analysis of warfarin enantiomers in human plasma
    • Naidong W., Ring P.R., Midtlien C., Jiang X. Development and validation of a sensitive and robust LC-tandem MS method for the analysis of warfarin enantiomers in human plasma. J. Pharm. Biomed. Anal. 25:2001;219-226.
    • (2001) J. Pharm. Biomed. Anal. , vol.25 , pp. 219-226
    • Naidong, W.1    Ring, P.R.2    Midtlien, C.3    Jiang, X.4
  • 99
    • 0033959516 scopus 로고    scopus 로고
    • Reliable assay of extreme enantiomeric purity values by a new circular dichroism based HPLC detection system
    • Bertucci C., Andrisano V., Cavrini V., Castiglioni E. Reliable assay of extreme enantiomeric purity values by a new circular dichroism based HPLC detection system. Chirality. 12:2000;84-92.
    • (2000) Chirality , vol.12 , pp. 84-92
    • Bertucci, C.1    Andrisano, V.2    Cavrini, V.3    Castiglioni, E.4
  • 100
    • 0034717103 scopus 로고    scopus 로고
    • Sensitive stereospecific determination of acenocoumarol and phenprocoumon in plasma by high-performance liquid chromatography
    • Rentsch K.M., Gutteck-Amsler U., Bührer R., Fattinger K.E., Vonderschmitt D.J. Sensitive stereospecific determination of acenocoumarol and phenprocoumon in plasma by high-performance liquid chromatography. J. Chromatogr. B. 742:2000;131-142.
    • (2000) J. Chromatogr. B , vol.742 , pp. 131-142
    • Rentsch, K.M.1    Gutteck-Amsler, U.2    Bührer, R.3    Fattinger, K.E.4    Vonderschmitt, D.J.5
  • 101
    • 0031667560 scopus 로고    scopus 로고
    • Stereoselective analysis of benazepril and its stereoisomers by reversed-phase high-performance liquid chromatography on a chiral AGP column
    • Cirilli R., La Torre F. Stereoselective analysis of benazepril and its stereoisomers by reversed-phase high-performance liquid chromatography on a chiral AGP column. J. Chromatogr. A. 818:1998;53-60.
    • (1998) J. Chromatogr. A , vol.818 , pp. 53-60
    • Cirilli, R.1    La Torre, F.2
  • 102
    • 0032811186 scopus 로고    scopus 로고
    • Stereoselective analysis of idrapril and its stereoisomers by reversed-phase high-performance liquid chromatography on a chiral AGP column
    • Cirilli R., Di Bugno C., La Torre F. Stereoselective analysis of idrapril and its stereoisomers by reversed-phase high-performance liquid chromatography on a chiral AGP column. Chromatographia. 49:1999;628-634.
    • (1999) Chromatographia , vol.49 , pp. 628-634
    • Cirilli, R.1    Di Bugno, C.2    La Torre, F.3
  • 103
    • 0035002392 scopus 로고    scopus 로고
    • Direct separation of captopril diastereoisomers including their rotational isomers by RP-LC using a teicoplanin column
    • Owens P.K., Svensson L.A., Vessman J. Direct separation of captopril diastereoisomers including their rotational isomers by RP-LC using a teicoplanin column. J. Pharm. Biomed. Anal. 25:2001;453-464.
    • (2001) J. Pharm. Biomed. Anal. , vol.25 , pp. 453-464
    • Owens, P.K.1    Svensson, L.A.2    Vessman, J.3
  • 104
    • 0343618773 scopus 로고    scopus 로고
    • Chromatographic separation of chlorthalidone enantiomers using β-cyclodextrins as chiral additives
    • Herráez-Hernández R., Campíns-Falcó P. Chromatographic separation of chlorthalidone enantiomers using β-cyclodextrins as chiral additives. J. Chromatogr. B. 740:2000;169-177.
    • (2000) J. Chromatogr. B , vol.740 , pp. 169-177
    • Herráez-Hernández, R.1    Campíns-Falcó, P.2
  • 105
    • 0035929477 scopus 로고    scopus 로고
    • Chiral supercritical fluid chromatography on porous graphitic carbon using commercial dimethyl β-cyclodextrins as mobile phase additive
    • Salvador A., Herbreteau B., Dreux M., Karlsson A., Gyllenhaal O. Chiral supercritical fluid chromatography on porous graphitic carbon using commercial dimethyl β-cyclodextrins as mobile phase additive. J. Chromatogr. A. 929:2001;101-112.
    • (2001) J. Chromatogr. A , vol.929 , pp. 101-112
    • Salvador, A.1    Herbreteau, B.2    Dreux, M.3    Karlsson, A.4    Gyllenhaal, O.5
  • 106
    • 0030908479 scopus 로고    scopus 로고
    • Determination of p-hydroxymandelic acid enantiomers in urine by high-performance liquid chromatography with electrochemical detection
    • Arai K., Jin D., Kusu F., Takamura K. Determination of p-hydroxymandelic acid enantiomers in urine by high-performance liquid chromatography with electrochemical detection. J. Pharm. Biomed. Anal. 15:1997;1509-1514.
    • (1997) J. Pharm. Biomed. Anal. , vol.15 , pp. 1509-1514
    • Arai, K.1    Jin, D.2    Kusu, F.3    Takamura, K.4
  • 107
    • 0031941404 scopus 로고    scopus 로고
    • HPLC separation of metyrosine enantiomers as methyl esters derivatized with 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate
    • Hefnawy M.M., Stewart J.T. HPLC separation of metyrosine enantiomers as methyl esters derivatized with 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate. J. Liq. Chromatogr. Relat. Technol. 21:1998;381-389.
    • (1998) J. Liq. Chromatogr. Relat. Technol. , vol.21 , pp. 381-389
    • Hefnawy, M.M.1    Stewart, J.T.2
  • 108
    • 0032729013 scopus 로고    scopus 로고
    • Direct chromatographic resolution and isolation of the four stereoisomers of meta-hydroxyphenylpropanolamine
    • Van Dort M.E. Direct chromatographic resolution and isolation of the four stereoisomers of meta-hydroxyphenylpropanolamine. Chirality. 11:1999;684-688.
    • (1999) Chirality , vol.11 , pp. 684-688
    • Van Dort, M.E.1
  • 109
    • 0346686877 scopus 로고    scopus 로고
    • Enantioselectivity of debrisoquine 4-hydroxylation in Brazilian Caucasian hypertensive patients phenotyped as extensive metabolizers
    • Cerqueira P.M., Mateus F.H., Cesarino E.J., Bonato P.S., Lanchote V.L. Enantioselectivity of debrisoquine 4-hydroxylation in Brazilian Caucasian hypertensive patients phenotyped as extensive metabolizers. J. Chromatogr. B. 749:2000;153-161.
    • (2000) J. Chromatogr. B , vol.749 , pp. 153-161
    • Cerqueira, P.M.1    Mateus, F.H.2    Cesarino, E.J.3    Bonato, P.S.4    Lanchote, V.L.5
  • 110
    • 0030888416 scopus 로고    scopus 로고
    • Steady-state clearance rates of warfarin and its enantiomers in therapeutically dosed patients
    • McAleer S.D., Foondun A.S., Feely M., Chrystyn H. Steady-state clearance rates of warfarin and its enantiomers in therapeutically dosed patients. Chirality. 9:1997;13-16.
    • (1997) Chirality , vol.9 , pp. 13-16
    • McAleer, S.D.1    Foondun, A.S.2    Feely, M.3    Chrystyn, H.4
  • 111
    • 0030694223 scopus 로고    scopus 로고
    • Species differences for stereoselective hydrolysis of propranolol prodrugs in plasma and liver
    • Yoshigae Y., Imai T., Horita A., Otagiri M. Species differences for stereoselective hydrolysis of propranolol prodrugs in plasma and liver. Chirality. 9:1997;661-666.
    • (1997) Chirality , vol.9 , pp. 661-666
    • Yoshigae, Y.1    Imai, T.2    Horita, A.3    Otagiri, M.4
  • 112
    • 0030960018 scopus 로고    scopus 로고
    • Stereoselective metabolism of rac-mexiletine by the fungus cunninghamella echinulata yields the major human metabolites hydroxymethylmexiletine and p-hydroxymexiletine
    • Freitag D.G., Foster R.T., Coutts R.T., Pickard M.A., Pasutto F.M. Stereoselective metabolism of rac-mexiletine by the fungus cunninghamella echinulata yields the major human metabolites hydroxymethylmexiletine and p-hydroxymexiletine. Drug Metab. Dispos. 25:1997;685-692.
    • (1997) Drug Metab. Dispos. , vol.25 , pp. 685-692
    • Freitag, D.G.1    Foster, R.T.2    Coutts, R.T.3    Pickard, M.A.4    Pasutto, F.M.5
  • 113
    • 0030907494 scopus 로고    scopus 로고
    • Pharmacokinetics and pharmacodynamics of pirmentol enantiomers in coronary artery ligated dogs
    • Janiczek N., Smith D.E., Chang T., Ventura A., Mertz T.E. Pharmacokinetics and pharmacodynamics of pirmentol enantiomers in coronary artery ligated dogs. J. Pharm. Sci. 86:1997;443-449.
    • (1997) J. Pharm. Sci. , vol.86 , pp. 443-449
    • Janiczek, N.1    Smith, D.E.2    Chang, T.3    Ventura, A.4    Mertz, T.E.5
  • 114
    • 0030995437 scopus 로고    scopus 로고
    • Stereoselective pharmacokinetics of bisoprolol after intravenous and oral administration in beagle dogs
    • Horikiri Y., Suzuki T., Mizobe M. Stereoselective pharmacokinetics of bisoprolol after intravenous and oral administration in beagle dogs. J. Pharm. Sci. 86:1997;560-564.
    • (1997) J. Pharm. Sci. , vol.86 , pp. 560-564
    • Horikiri, Y.1    Suzuki, T.2    Mizobe, M.3
  • 115
    • 0031924807 scopus 로고    scopus 로고
    • Pharmacokinetics and metabolism of bisoprolol enantiomers in humans
    • Horikiri Y., Suzuki T., Mizobe M. Pharmacokinetics and metabolism of bisoprolol enantiomers in humans. J. Pharm. Sci. 87:1998;289-294.
    • (1998) J. Pharm. Sci. , vol.87 , pp. 289-294
    • Horikiri, Y.1    Suzuki, T.2    Mizobe, M.3
  • 116
    • 0032555318 scopus 로고    scopus 로고
    • Stereoselective metabolism of bisoprolol enantiomers in dogs and humans
    • Horikiri Y., Suzuki T., Mizobe M. Stereoselective metabolism of bisoprolol enantiomers in dogs and humans. Life Sci. 63:1998;1097-1108.
    • (1998) Life Sci. , vol.63 , pp. 1097-1108
    • Horikiri, Y.1    Suzuki, T.2    Mizobe, M.3
  • 117
    • 0031902427 scopus 로고    scopus 로고
    • Steady-state pharmacokinetics of propranolol enantiomers in healthy male volunteers
    • Paradiso-Hardy F.L., Walker S.E., Bowles S.K. Steady-state pharmacokinetics of propranolol enantiomers in healthy male volunteers. Int. J. Clin. Pharmacol. Ther. 36:1998;370-375.
    • (1998) Int. J. Clin. Pharmacol. Ther. , vol.36 , pp. 370-375
    • Paradiso-Hardy, F.L.1    Walker, S.E.2    Bowles, S.K.3
  • 118
    • 6844255207 scopus 로고    scopus 로고
    • The enantiomer-specific kinetics and dynamics of verapamil after rapid intravenous administration to sheep: Physiological analysis and modeling
    • Huang Y.F., Upton R.N., Zheng D., McLean C., Gray E.C., Grant C. The enantiomer-specific kinetics and dynamics of verapamil after rapid intravenous administration to sheep: physiological analysis and modeling. J. Pharmacol. Exp. Ther. 284:1998;1048-1057.
    • (1998) J. Pharmacol. Exp. Ther. , vol.284 , pp. 1048-1057
    • Huang, Y.F.1    Upton, R.N.2    Zheng, D.3    McLean, C.4    Gray, E.C.5    Grant, C.6
  • 119
    • 0031687711 scopus 로고    scopus 로고
    • Pharmacokinetics of single oral and multiple intravenous and oral administration of acebutolol enantiomers in a rat model
    • Mostafavi S.A., Foster R.T. Pharmacokinetics of single oral and multiple intravenous and oral administration of acebutolol enantiomers in a rat model. Biopharm. Drug Dispos. 19:1998;425-431.
    • (1998) Biopharm. Drug Dispos. , vol.19 , pp. 425-431
    • Mostafavi, S.A.1    Foster, R.T.2
  • 120
    • 0032954533 scopus 로고    scopus 로고
    • Stereoselective disposition of the antiarrhythmic agent mexiletine during the concomitant administration of caffeine
    • Labbé L., Abolfathi Z., Robitaille N.M., St-Maurice F., Gilbert M., Turgeon J. Stereoselective disposition of the antiarrhythmic agent mexiletine during the concomitant administration of caffeine. Ther. Drug Monit. 21:1999;191-199.
    • (1999) Ther. Drug Monit. , vol.21 , pp. 191-199
    • Labbé, L.1    Abolfathi, Z.2    Robitaille, N.M.3    St-Maurice, F.4    Gilbert, M.5    Turgeon, J.6
  • 121
    • 0032928458 scopus 로고    scopus 로고
    • Enantioselectivity in the metabolism of mexiletine by conjugation in female patients with the arrhythmic form of chronic Chagas' heart disease
    • Lanchote L.V., Cesarino E.J., Santos V.J., Mere Y. Jr., Santos S.R.C.J. Enantioselectivity in the metabolism of mexiletine by conjugation in female patients with the arrhythmic form of chronic Chagas' heart disease. Chirality. 11:1999;29-32.
    • (1999) Chirality , vol.11 , pp. 29-32
    • Lanchote, L.V.1    Cesarino, E.J.2    Santos, V.J.3    Mere Y., Jr.4    Santos, S.R.C.J.5
  • 122
    • 0032894348 scopus 로고    scopus 로고
    • Enantioselective analysis of N-hydroxymexiletine glucuronide in human plasma for pharmacokinetic studies
    • Lanchote L.V., Santos V.J., Cesarino E.J., Dreossi S.A.C., Mere Y. Jr., Santos S.R.C.J. Enantioselective analysis of N-hydroxymexiletine glucuronide in human plasma for pharmacokinetic studies. Chirality. 11:1999;85-90.
    • (1999) Chirality , vol.11 , pp. 85-90
    • Lanchote, L.V.1    Santos, V.J.2    Cesarino, E.J.3    Dreossi, S.A.C.4    Mere Y., Jr.5    Santos, S.R.C.J.6
  • 125
    • 0034040010 scopus 로고    scopus 로고
    • Gender differences in labetalol kinetics: Importance of determining stereoisomer kinetics for racemic drugs
    • Johnson J.A., Akers W.S., Herring V.L., Wolfe M.S., Sullivan J.M. Gender differences in labetalol kinetics: importance of determining stereoisomer kinetics for racemic drugs. Pharmacotherapy. 20:2000;622-628.
    • (2000) Pharmacotherapy , vol.20 , pp. 622-628
    • Johnson, J.A.1    Akers, W.S.2    Herring, V.L.3    Wolfe, M.S.4    Sullivan, J.M.5
  • 126
    • 0034049593 scopus 로고    scopus 로고
    • Stereoselective pharmacokinetics of propafenone and its major metabolites in healthy Chinese volunteers
    • Chen X., Zhong D., Blume H. Stereoselective pharmacokinetics of propafenone and its major metabolites in healthy Chinese volunteers. Eur. J. Pharm. Sci. 10:2000;11-16.
    • (2000) Eur. J. Pharm. Sci. , vol.10 , pp. 11-16
    • Chen, X.1    Zhong, D.2    Blume, H.3
  • 127
    • 0033928135 scopus 로고    scopus 로고
    • β-Agonist-induced alterations in organ weights and protein content: Comparison of racemic clenbuterol and its enantiomers
    • Von Deutsch D.A., Abukhalaf I.K., Wineski L.E., Aboul-Enein H.Y., Pitts S.A., Parks B.A.et al. β-Agonist-induced alterations in organ weights and protein content: comparison of racemic clenbuterol and its enantiomers. Chirality. 12:2000;637-648.
    • (2000) Chirality , vol.12 , pp. 637-648
    • Von Deutsch, D.A.1    Abukhalaf, I.K.2    Wineski, L.E.3    Aboul-Enein, H.Y.4    Pitts, S.A.5    Parks, B.A.6
  • 128
    • 0034424762 scopus 로고    scopus 로고
    • Studies on concentration-time profiles of nimodipine enantiomers following intravenous and oral administration of nimodipine in patients with subarachnoid hemorrhage
    • Wanner-Olsen H., Gaarskaer F.B., Mikkelsen E.O., Jacobsen P., Voldby B. Studies on concentration-time profiles of nimodipine enantiomers following intravenous and oral administration of nimodipine in patients with subarachnoid hemorrhage. Chirality. 12:2000;660-664.
    • (2000) Chirality , vol.12 , pp. 660-664
    • Wanner-Olsen, H.1    Gaarskaer, F.B.2    Mikkelsen, E.O.3    Jacobsen, P.4    Voldby, B.5
  • 129
    • 0034939639 scopus 로고    scopus 로고
    • Stereoselective pharmacokinetics and pharmacodynamics of verapamil and norverapamil in rabbits
    • Mori Y., Hanada K., Mori T., Tsukahara Y., Hashiguchi M., Ogata H. Stereoselective pharmacokinetics and pharmacodynamics of verapamil and norverapamil in rabbits. Biol. Pharm. Bull. 24:2001;806-810.
    • (2001) Biol. Pharm. Bull. , vol.24 , pp. 806-810
    • Mori, Y.1    Hanada, K.2    Mori, T.3    Tsukahara, Y.4    Hashiguchi, M.5    Ogata, H.6
  • 130
    • 0035114228 scopus 로고    scopus 로고
    • High performance liquid chromatographic analysis of the sulfation of 4-hydroxypropranolol enantiomers by monkey liver cytosol
    • Narimatsu S., Kobayashi N., Asaoka K., Masubuchi Y., Horie T., Hosokawa M.et al. High performance liquid chromatographic analysis of the sulfation of 4-hydroxypropranolol enantiomers by monkey liver cytosol. Chirality. 13:2001;140-147.
    • (2001) Chirality , vol.13 , pp. 140-147
    • Narimatsu, S.1    Kobayashi, N.2    Asaoka, K.3    Masubuchi, Y.4    Horie, T.5    Hosokawa, M.6
  • 131
    • 0031006490 scopus 로고    scopus 로고
    • Enantioselective retardation of rac-propranolol from matrices containing cellulose derivatives
    • Suedee R., Brain K.R., Heard C.M. Enantioselective retardation of rac-propranolol from matrices containing cellulose derivatives. Chirality. 9:1997;307-312.
    • (1997) Chirality , vol.9 , pp. 307-312
    • Suedee, R.1    Brain, K.R.2    Heard, C.M.3
  • 132
    • 0032723185 scopus 로고    scopus 로고
    • Differential permeation of propranolol across human skin in vitro from formulations containing an enantioselective excipient
    • Suedee R., Brain K.R., Heard C.M. Differential permeation of propranolol across human skin in vitro from formulations containing an enantioselective excipient. Chirality. 11:1999;680-683.
    • (1999) Chirality , vol.11 , pp. 680-683
    • Suedee, R.1    Brain, K.R.2    Heard, C.M.3
  • 134
    • 0032920847 scopus 로고    scopus 로고
    • Synthesis, stereoselective enzymatic hydrolysis, and skin permeation of diastereomeric propranolol ester prodrugs
    • Udata C., Tirucherai G., Mitra A.K. Synthesis, stereoselective enzymatic hydrolysis, and skin permeation of diastereomeric propranolol ester prodrugs. J. Pharm. Sci. 88:1999;544-550.
    • (1999) J. Pharm. Sci. , vol.88 , pp. 544-550
    • Udata, C.1    Tirucherai, G.2    Mitra, A.K.3
  • 136
    • 0034923970 scopus 로고    scopus 로고
    • Methodologies for the stereoselective synthesis of adrenergic β-blockers: An overview
    • Campo C., Llama E.F., Bermúdez J.L., Sinisterra J.V. Methodologies for the stereoselective synthesis of adrenergic β-blockers: an overview. Biocatal. Biotransform. 19:2001;163-180.
    • (2001) Biocatal. Biotransform. , vol.19 , pp. 163-180
    • Campo, C.1    Llama, E.F.2    Bermúdez, J.L.3    Sinisterra, J.V.4
  • 137
    • 0029971807 scopus 로고    scopus 로고
    • Flash chiral chromatography with cellulose tris(3,5-dimethylplenylcarbamate)-coated phases. Improved resolution of basic analytes
    • Grieb S.J., Matlin S.A., Belenguer A.M. Flash chiral chromatography with cellulose tris(3,5-dimethylplenylcarbamate)-coated phases. Improved resolution of basic analytes. J. Chromatogr. A. 728:1996;195-199.
    • (1996) J. Chromatogr. A , vol.728 , pp. 195-199
    • Grieb, S.J.1    Matlin, S.A.2    Belenguer, A.M.3
  • 138
    • 0030902531 scopus 로고    scopus 로고
    • Applications of simulated moving-bed chromatography to the separation of the enantiomers of chiral drugs
    • Francotte E.R., Richert P. Applications of simulated moving-bed chromatography to the separation of the enantiomers of chiral drugs. J. Chromatogr. A. 769:1997;101-107.
    • (1997) J. Chromatogr. A , vol.769 , pp. 101-107
    • Francotte, E.R.1    Richert, P.2
  • 139
    • 0032728523 scopus 로고    scopus 로고
    • Direct, preparative enantioselective chromatography of propranolol hydrochloride and thioridazine hydrochloride using carbon dioxide-based mobile phases
    • Geiser F., Schultz M., Betz L., Shaimi M., Lee J., Champion W. Jr. Direct, preparative enantioselective chromatography of propranolol hydrochloride and thioridazine hydrochloride using carbon dioxide-based mobile phases. J. Chromatogr. A. 865:1999;227-233.
    • (1999) J. Chromatogr. A , vol.865 , pp. 227-233
    • Geiser, F.1    Schultz, M.2    Betz, L.3    Shaimi, M.4    Lee, J.5    Champion W., Jr.6
  • 140
    • 0030580996 scopus 로고    scopus 로고
    • Regioselective carbamoylated and benzoylated cellulose for the separation of enantiomers in high-performance liquid chromatography
    • Chassaing C., Thienpont A., Felix G. Regioselective carbamoylated and benzoylated cellulose for the separation of enantiomers in high-performance liquid chromatography. J. Chromatogr. A. 738:1996;157-167.
    • (1996) J. Chromatogr. A , vol.738 , pp. 157-167
    • Chassaing, C.1    Thienpont, A.2    Felix, G.3
  • 141
    • 0029901310 scopus 로고    scopus 로고
    • Bonded cellulose-derived high-performance liquid chromatography chiral stationary phases: I. Influence of the degree of fixation on selectivity
    • Minguillón C., Franco P., Oliveros L., López P. Bonded cellulose-derived high-performance liquid chromatography chiral stationary phases: I. Influence of the degree of fixation on selectivity. J. Chromatogr. A. 728:1996;407-414.
    • (1996) J. Chromatogr. A , vol.728 , pp. 407-414
    • Minguillón, C.1    Franco, P.2    Oliveros, L.3    López, P.4
  • 142
    • 0029994678 scopus 로고    scopus 로고
    • Bonded cellulose-derived high-performance liquid chromatography chiral stationary phases: II. Influence of the porosity of the silica gel matrix on performance
    • Minguillón C., Franco P., Oliveros L. Bonded cellulose-derived high-performance liquid chromatography chiral stationary phases: II. Influence of the porosity of the silica gel matrix on performance. J. Chromatogr. A. 728:1996;415-422.
    • (1996) J. Chromatogr. A , vol.728 , pp. 415-422
    • Minguillón, C.1    Franco, P.2    Oliveros, L.3
  • 143
    • 0032536137 scopus 로고    scopus 로고
    • Solvent versatility of bonded chiral stationary phases for high-performance liquid chromatography and its consequences in column loadability
    • Franco P., Minguillón C., Oliveros L. Solvent versatility of bonded chiral stationary phases for high-performance liquid chromatography and its consequences in column loadability. J. Chromatogr. A. 793:1998;239-247.
    • (1998) J. Chromatogr. A , vol.793 , pp. 239-247
    • Franco, P.1    Minguillón, C.2    Oliveros, L.3
  • 144
    • 0000744206 scopus 로고    scopus 로고
    • Pressure-induced changes in chiral separations in liquid chromatography
    • Ringo M.C., Evans C.E. Pressure-induced changes in chiral separations in liquid chromatography. Anal. Chem. 69:1997;4964-4971.
    • (1997) Anal. Chem. , vol.69 , pp. 4964-4971
    • Ringo, M.C.1    Evans, C.E.2
  • 145
    • 0031565877 scopus 로고    scopus 로고
    • Bonded cellulose-derived high-performance liquid chromatography chiral stationary phases: III. Effect of the reticulation of the cellulose derivative on performance
    • Franco P., Minguillón C., Oliveros L. Bonded cellulose-derived high-performance liquid chromatography chiral stationary phases: III. Effect of the reticulation of the cellulose derivative on performance. J. Chromatogr. A. 791:1997;37-44.
    • (1997) J. Chromatogr. A , vol.791 , pp. 37-44
    • Franco, P.1    Minguillón, C.2    Oliveros, L.3
  • 146
    • 0031833968 scopus 로고    scopus 로고
    • Carbamates of cellulose bonded on silica gel: Chiral discrimination ability as HPLC chiral stationary phases
    • Oliveros L., Senso A., Franco P., Minguillón C. Carbamates of cellulose bonded on silica gel: chiral discrimination ability as HPLC chiral stationary phases. Chirality. 10:1998;283-288.
    • (1998) Chirality , vol.10 , pp. 283-288
    • Oliveros, L.1    Senso, A.2    Franco, P.3    Minguillón, C.4
  • 147
    • 0032548911 scopus 로고    scopus 로고
    • 3,5-Dimethylphenylcarbamates of amylose, chitosan and cellulose bonded to silica gel. Comparison of their chiral recognition abilities as high-performance liquid chromatography stationary phases
    • Franco P., Senso A., Minguillón C., Oliveros L. 3,5-Dimethylphenylcarbamates of amylose, chitosan and cellulose bonded to silica gel. Comparison of their chiral recognition abilities as high-performance liquid chromatography stationary phases. J. Chromatogr. A. 796:1998;265-272.
    • (1998) J. Chromatogr. A , vol.796 , pp. 265-272
    • Franco, P.1    Senso, A.2    Minguillón, C.3    Oliveros, L.4
  • 148
    • 0032837055 scopus 로고    scopus 로고
    • Reversed-phase separations on cellulose tris(3,5-dimethylphenylcarbamate) chiral stationary phase
    • Hou J.G., Wang Y.L., Li C.X., Han X.Q., Gao J.Z., Kang J.W. Reversed-phase separations on cellulose tris(3,5-dimethylphenylcarbamate) chiral stationary phase. Chromatographia. 50:1999;89-95.
    • (1999) Chromatographia , vol.50 , pp. 89-95
    • Hou, J.G.1    Wang, Y.L.2    Li, C.X.3    Han, X.Q.4    Gao, J.Z.5    Kang, J.W.6
  • 149
    • 0032719581 scopus 로고    scopus 로고
    • Enantioseparation on amylose tris(3,5-dimethoxyphenyl carbamate): Application to commercial pharmaceutical chiral drugs
    • Cass Q.B., Tiritan M.E., Calafatti S.A., Matlin S.A. Enantioseparation on amylose tris(3,5-dimethoxyphenyl carbamate): application to commercial pharmaceutical chiral drugs. J. Liq. Chromatogr. Relat. Technol. 22:1999;3091-3099.
    • (1999) J. Liq. Chromatogr. Relat. Technol. , vol.22 , pp. 3091-3099
    • Cass, Q.B.1    Tiritan, M.E.2    Calafatti, S.A.3    Matlin, S.A.4
  • 150
    • 0034525614 scopus 로고    scopus 로고
    • Enantioseparations using cellulose tris(3,5dichlorophenylcarbamate) during high-performance liquid chromatography with analytical capillary columns: Potential for screening of chiral drugs
    • Chankvetadze B., Yamamoto C., Okamoto Y. Enantioseparations using cellulose tris(3,5dichlorophenylcarbamate) during high-performance liquid chromatography with analytical capillary columns: potential for screening of chiral drugs. Combin. Chem. High Throughput Screen. 3:2000;497-508.
    • (2000) Combin. Chem. High Throughput Screen. , vol.3 , pp. 497-508
    • Chankvetadze, B.1    Yamamoto, C.2    Okamoto, Y.3
  • 151
    • 0034634713 scopus 로고    scopus 로고
    • Effect of mobile phase composition on the separation of propranolol enantiomers using a perphenylcarbamate β-cyclodextrin bonded chiral stationary phase
    • Ching C.B., Fu P., Ng S.C., Xu Y.K. Effect of mobile phase composition on the separation of propranolol enantiomers using a perphenylcarbamate β-cyclodextrin bonded chiral stationary phase. J. Chromatogr. A. 898:2000;53-61.
    • (2000) J. Chromatogr. A , vol.898 , pp. 53-61
    • Ching, C.B.1    Fu, P.2    Ng, S.C.3    Xu, Y.K.4
  • 152
    • 0034704440 scopus 로고    scopus 로고
    • Fast separations of basic analytes by high-performance liquid chromatography using cellulose tris(3,5-dimethylphenylcarbamate)-coated zirconia stationary phases
    • Castells C.B., Carr P.W. Fast separations of basic analytes by high-performance liquid chromatography using cellulose tris(3,5-dimethylphenylcarbamate)-coated zirconia stationary phases. J. Chromatogr. A. 904:2000;17-33.
    • (2000) J. Chromatogr. A , vol.904 , pp. 17-33
    • Castells, C.B.1    Carr, P.W.2
  • 153
    • 0035946245 scopus 로고    scopus 로고
    • Study of the retention properties of warfarin enantiomers on a β-cyclodextrin polymeric support
    • Guillaume M., Jaulmes A., Sébille B., Thuaud N., Vidal-Madjar C. Study of the retention properties of warfarin enantiomers on a β-cyclodextrin polymeric support. J. Chromatogr. B. 753:2001;131-138.
    • (2001) J. Chromatogr. B , vol.753 , pp. 131-138
    • Guillaume, M.1    Jaulmes, A.2    Sébille, B.3    Thuaud, N.4    Vidal-Madjar, C.5
  • 154
    • 0031828171 scopus 로고    scopus 로고
    • Highly selective HPLC separations using the covalently bonded macrocyclic antibiotic, ristocetin A, chiral stationary phase
    • Ekborg-Ott K.H., Liu Y., Armstrong D.W. Highly selective HPLC separations using the covalently bonded macrocyclic antibiotic, ristocetin A, chiral stationary phase. Chirality. 10:1998;434-483.
    • (1998) Chirality , vol.10 , pp. 434-483
    • Ekborg-Ott, K.H.1    Liu, Y.2    Armstrong, D.W.3
  • 155
    • 0031680597 scopus 로고    scopus 로고
    • Evaluation of the macrocyclic antibiotic avoparcin as a new chiral selector for HPLC
    • Ekborg-Ott K.H., Kullman J.P., Wang X., Gahm K., He L., Armstrong D.W. Evaluation of the macrocyclic antibiotic avoparcin as a new chiral selector for HPLC. Chirality. 10:1998;627-660.
    • (1998) Chirality , vol.10 , pp. 627-660
    • Ekborg-Ott, K.H.1    Kullman, J.P.2    Wang, X.3    Gahm, K.4    He, L.5    Armstrong, D.W.6
  • 156
    • 0344076242 scopus 로고    scopus 로고
    • Vancomycin-based chiral stationary phases for micro-column liquid chromatography
    • Svensson L.A., Dönnecke J., Karlsson K.-E., Karlsson A., Vessman J. Vancomycin-based chiral stationary phases for micro-column liquid chromatography. Chirality. 11:1999;121-128.
    • (1999) Chirality , vol.11 , pp. 121-128
    • Svensson, L.A.1    Dönnecke, J.2    Karlsson, K.-E.3    Karlsson, A.4    Vessman, J.5
  • 157
    • 0034048114 scopus 로고    scopus 로고
    • Enantioselective supercritical fluid chromatography using ristocetin A chiral stationary phases
    • Svensson L.A., Owens P.K. Enantioselective supercritical fluid chromatography using ristocetin A chiral stationary phases. Analyst. 125:2000;1037-1039.
    • (2000) Analyst , vol.125 , pp. 1037-1039
    • Svensson, L.A.1    Owens, P.K.2
  • 158
    • 0034655855 scopus 로고    scopus 로고
    • Role of the carbohydrate moieties in chiral recognition on teicoplanin-based LC stationary phases
    • Berthod A., Chen X., Kullman J.P., Armstrong D.W., Gasparrini F., D'Acquarica I.et al. Role of the carbohydrate moieties in chiral recognition on teicoplanin-based LC stationary phases. Anal. Chem. 72:2000;1767-1780.
    • (2000) Anal. Chem. , vol.72 , pp. 1767-1780
    • Berthod, A.1    Chen, X.2    Kullman, J.P.3    Armstrong, D.W.4    Gasparrini, F.5    D'Acquarica, I.6
  • 159
    • 0343962232 scopus 로고    scopus 로고
    • Polar organic phase liquid chromatography with packed capillary columns using a vancomycic chiral stationary phase
    • Svensson L.A., Dönnecke J., Karlsson K.-E., Karlsson A., Vessman J. Polar organic phase liquid chromatography with packed capillary columns using a vancomycic chiral stationary phase. Chirality. 12:2000;606-613.
    • (2000) Chirality , vol.12 , pp. 606-613
    • Svensson, L.A.1    Dönnecke, J.2    Karlsson, K.-E.3    Karlsson, A.4    Vessman, J.5
  • 160
    • 0034602469 scopus 로고    scopus 로고
    • Evaluation of the macrocyclic glycopeptide A-40,926 as a high-performance liquid chromatographic chiral selector and comparison with teicoplanin chiral stationary phase
    • Berthod A., Yu T., Kullman J.P., Armstrong D.W., Gasparrini F., D'Acquarica I.et al. Evaluation of the macrocyclic glycopeptide A-40,926 as a high-performance liquid chromatographic chiral selector and comparison with teicoplanin chiral stationary phase. J. Chromatogr. A. 897:2000;113-129.
    • (2000) J. Chromatogr. A , vol.897 , pp. 113-129
    • Berthod, A.1    Yu, T.2    Kullman, J.P.3    Armstrong, D.W.4    Gasparrini, F.5    D'Acquarica, I.6
  • 161
    • 0031588705 scopus 로고    scopus 로고
    • Influence of chromatographic descriptors on enantioresolution of a dihydropyridine and structurally related compounds
    • Gottfries J., Johansson P., Karlsson A. Influence of chromatographic descriptors on enantioresolution of a dihydropyridine and structurally related compounds. J. Chromatogr. A. 763:1997;115-123.
    • (1997) J. Chromatogr. A , vol.763 , pp. 115-123
    • Gottfries, J.1    Johansson, P.2    Karlsson, A.3
  • 162
    • 0031006974 scopus 로고    scopus 로고
    • Enantioselectivity of bovine serum albumin-bonded columns produced with isolated protein fragments: II. Characterization of protein fragments and chiral binding sites
    • Haginaka J., Kanasugi N. Enantioselectivity of bovine serum albumin-bonded columns produced with isolated protein fragments: II. Characterization of protein fragments and chiral binding sites. J. Chromatogr. A. 769:1997;215-223.
    • (1997) J. Chromatogr. A , vol.769 , pp. 215-223
    • Haginaka, J.1    Kanasugi, N.2
  • 163
    • 0343812109 scopus 로고    scopus 로고
    • Enantiomeric properties of human albumin immobilized on porous silica supports coated with polymethacryloyl chloride
    • Millot M.C., Sébille B., Mangin C. Enantiomeric properties of human albumin immobilized on porous silica supports coated with polymethacryloyl chloride. J. Chromatogr. A. 776:1997;37-44.
    • (1997) J. Chromatogr. A , vol.776 , pp. 37-44
    • Millot, M.C.1    Sébille, B.2    Mangin, C.3
  • 164
    • 0030788053 scopus 로고    scopus 로고
    • Improved chromatographic performance of a modified human albumin based stationary phase
    • Bertucci C., Wainer I.W. Improved chromatographic performance of a modified human albumin based stationary phase. Chirality. 9:1997;335-340.
    • (1997) Chirality , vol.9 , pp. 335-340
    • Bertucci, C.1    Wainer, I.W.2
  • 165
    • 0031687538 scopus 로고    scopus 로고
    • Stereoselective binding of warfarin and ketoprofen to human serum albumin determined by microdialysis combined with HPLC
    • Zou H., Wang H., Zhang Y. Stereoselective binding of warfarin and ketoprofen to human serum albumin determined by microdialysis combined with HPLC. J. Liq. Chromatogr. Relat. Technol. 21:1998;2663-2674.
    • (1998) J. Liq. Chromatogr. Relat. Technol. , vol.21 , pp. 2663-2674
    • Zou, H.1    Wang, H.2    Zhang, Y.3
  • 166
    • 0031670210 scopus 로고    scopus 로고
    • Ligand binding to a human serum albumin stationary phase: Use of same-drug competition to discriminate pharmacologically relevant interactions
    • Ascoli G.A., Bertucci C., Salvadori P. Ligand binding to a human serum albumin stationary phase: use of same-drug competition to discriminate pharmacologically relevant interactions. Biomed. Chromatogr. 12:1998;248-254.
    • (1998) Biomed. Chromatogr. , vol.12 , pp. 248-254
    • Ascoli, G.A.1    Bertucci, C.2    Salvadori, P.3
  • 168
    • 0033387015 scopus 로고    scopus 로고
    • Chromatographic properties of chiral stationary phases based on human serum albumin. Influence of the polymer sublayer
    • Millot M.C., Loehman L., Sébille B., Hommel H. Chromatographic properties of chiral stationary phases based on human serum albumin. Influence of the polymer sublayer. Chromatographia. 50:1999;641-648.
    • (1999) Chromatographia , vol.50 , pp. 641-648
    • Millot, M.C.1    Loehman, L.2    Sébille, B.3    Hommel, H.4
  • 169
    • 0033826547 scopus 로고    scopus 로고
    • Development of a disulfiram-modified human serum albumin-based HPLC column
    • Bertucci C., Andrisano V., Gotti R., Cavrini V. Development of a disulfiram-modified human serum albumin-based HPLC column. Chromatographia. 52:2000;319-324.
    • (2000) Chromatographia , vol.52 , pp. 319-324
    • Bertucci, C.1    Andrisano, V.2    Gotti, R.3    Cavrini, V.4
  • 170
    • 0033992447 scopus 로고    scopus 로고
    • Synthesis of a silica-bonded bovine serum albumin s-triazine chiral stationary phase for high-performance liquid chromatographic resolution of enantiomers
    • Zhang Q., Zou H., Wang H., Ni J. Synthesis of a silica-bonded bovine serum albumin s-triazine chiral stationary phase for high-performance liquid chromatographic resolution of enantiomers. J. Chromatogr. A. 866:2000;173-181.
    • (2000) J. Chromatogr. A , vol.866 , pp. 173-181
    • Zhang, Q.1    Zou, H.2    Wang, H.3    Ni, J.4
  • 171
    • 0034969814 scopus 로고    scopus 로고
    • Modulation of chromatographic performances of HSA-based HPLC column by reversible binding of lithocholic acid
    • Bertucci C., Andrisano V., Gotti R., Cavrini V. Modulation of chromatographic performances of HSA-based HPLC column by reversible binding of lithocholic acid. Chromatographia. 53:2001;515-518.
    • (2001) Chromatographia , vol.53 , pp. 515-518
    • Bertucci, C.1    Andrisano, V.2    Gotti, R.3    Cavrini, V.4
  • 172
    • 0031473719 scopus 로고    scopus 로고
    • Evaluation of quail egg white riboflavin binding protein as a chiral selector in high-performance liquid chromatography and capillary electrophoresis
    • De Lorenzi E., Massolini G., Lloyd D.K., Monaco H.L., Galbusera C., Caccialanza G. Evaluation of quail egg white riboflavin binding protein as a chiral selector in high-performance liquid chromatography and capillary electrophoresis. J. Chromatogr. A. 790:1997;47-64.
    • (1997) J. Chromatogr. A , vol.790 , pp. 47-64
    • De Lorenzi, E.1    Massolini, G.2    Lloyd, D.K.3    Monaco, H.L.4    Galbusera, C.5    Caccialanza, G.6
  • 174
    • 0032493707 scopus 로고    scopus 로고
    • Evaluation of β-lactoglobulin as a stationary phase in high-performance liquid chromatography and as a buffer additive in capillary electrophoresis: Observation of a surprising lack of stereoselectivity
    • Massolini G., De Lorenzi E., Lloyd D.K., McGann A.M., Caccialanza G. Evaluation of β-lactoglobulin as a stationary phase in high-performance liquid chromatography and as a buffer additive in capillary electrophoresis: observation of a surprising lack of stereoselectivity. J. Chromatogr. B. 712:1998;83-94.
    • (1998) J. Chromatogr. B , vol.712 , pp. 83-94
    • Massolini, G.1    De Lorenzi, E.2    Lloyd, D.K.3    McGann, A.M.4    Caccialanza, G.5
  • 175
    • 0031928527 scopus 로고    scopus 로고
    • Unexpected difference in enantioselective retention on cellulase (CBH I) silica stationary phase caused by exchange of potassium for sodium ion in the mobile phase
    • Hedeland M., Jönsson S., Isaksson R., Pettersson C. Unexpected difference in enantioselective retention on cellulase (CBH I) silica stationary phase caused by exchange of potassium for sodium ion in the mobile phase. Chirality. 10:1998;513-518.
    • (1998) Chirality , vol.10 , pp. 513-518
    • Hedeland, M.1    Jönsson, S.2    Isaksson, R.3    Pettersson, C.4
  • 176
    • 0031697228 scopus 로고    scopus 로고
    • Chiral separations of selected pharmaceuticals on avidin column
    • Haque A., Stewart J.T. Chiral separations of selected pharmaceuticals on avidin column. J. Liq. Chromatogr. Relat. Technol. 21:1998;2675-2687.
    • (1998) J. Liq. Chromatogr. Relat. Technol. , vol.21 , pp. 2675-2687
    • Haque, A.1    Stewart, J.T.2
  • 177
    • 0031593819 scopus 로고    scopus 로고
    • 1-glycoprotein acid as chiral selector in the enantioseparation of midodrine and deglymidodrine racemates by HPLC
    • 1-glycoprotein acid as chiral selector in the enantioseparation of midodrine and deglymidodrine racemates by HPLC. J. Pharm. Biomed. Anal. 18:1998;171-177.
    • (1998) J. Pharm. Biomed. Anal. , vol.18 , pp. 171-177
    • Quaglia, M.G.1    Farina, A.2    Bossú, E.3    Cotichini, V.4
  • 178
    • 0032557592 scopus 로고    scopus 로고
    • Cellobiohydrolase I as a chiral additive in capillary electrophoresis and liquid chromatography
    • Hedeland M., Isaksson R., Pettersson C. Cellobiohydrolase I as a chiral additive in capillary electrophoresis and liquid chromatography. J. Chromatogr. A. 807:1998;297-305.
    • (1998) J. Chromatogr. A , vol.807 , pp. 297-305
    • Hedeland, M.1    Isaksson, R.2    Pettersson, C.3
  • 180
    • 0032791826 scopus 로고    scopus 로고
    • Stereochemical resolution of racemates, in HPLC, using a chiral stationary phase based upon immobilized α-chymotrypsin: I. Structural chiral separations
    • Félix G., Descorps V. Stereochemical resolution of racemates, in HPLC, using a chiral stationary phase based upon immobilized α-chymotrypsin: I. Structural chiral separations. Chromatographia. 49:1999;595-605.
    • (1999) Chromatographia , vol.49 , pp. 595-605
    • Félix, G.1    Descorps, V.2
  • 181
    • 0032899125 scopus 로고    scopus 로고
    • Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein
    • Haginaka J., Okazaki Y., Matsunaga H. Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein. J. Chromatogr. A. 840:1999;171-181.
    • (1999) J. Chromatogr. A , vol.840 , pp. 171-181
    • Haginaka, J.1    Okazaki, Y.2    Matsunaga, H.3
  • 182
    • 0032835772 scopus 로고    scopus 로고
    • Discrimination between enantioselective and non-selective binding sites on cellobiohydrolase-based stationary phases by site specific competing ligands
    • Henriksson H., Pettersson G., Johansson G. Discrimination between enantioselective and non-selective binding sites on cellobiohydrolase-based stationary phases by site specific competing ligands. J. Chromatogr. A. 857:1999.
    • (1999) J. Chromatogr. A , vol.857
    • Henriksson, H.1    Pettersson, G.2    Johansson, G.3
  • 183
    • 0032829544 scopus 로고    scopus 로고
    • Temperature-induced inversion of elution order in the enantioseparation of sotalol on a cellobiohydrolase I-based stationary phase
    • Fulde K., Frahm A.W. Temperature-induced inversion of elution order in the enantioseparation of sotalol on a cellobiohydrolase I-based stationary phase. J. Chromatogr. A. 858:1999;33-43.
    • (1999) J. Chromatogr. A , vol.858 , pp. 33-43
    • Fulde, K.1    Frahm, A.W.2
  • 184
    • 0032820016 scopus 로고    scopus 로고
    • Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein: VII. Comparison of chiral recognition ability of ovoglycoprotein from chicken and Japanese quail egg whites
    • Haginaka J., Kagawa C., Matsunaga H. Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein: VII. Comparison of chiral recognition ability of ovoglycoprotein from chicken and Japanese quail egg whites. J. Chromatogr. A. 858:1999;155-165.
    • (1999) J. Chromatogr. A , vol.858 , pp. 155-165
    • Haginaka, J.1    Kagawa, C.2    Matsunaga, H.3
  • 185
    • 0032752263 scopus 로고    scopus 로고
    • Chromatographic evaluation of structure selective and enantioselective retention of amines and acids on cellobiohydrolase I wild type and its mutant D214N
    • Hedeland M., Holmin S., Nygard M., Pettersson C. Chromatographic evaluation of structure selective and enantioselective retention of amines and acids on cellobiohydrolase I wild type and its mutant D214N. J. Chromatogr. A. 864:1999;1-16.
    • (1999) J. Chromatogr. A , vol.864 , pp. 1-16
    • Hedeland, M.1    Holmin, S.2    Nygard, M.3    Pettersson, C.4
  • 186
    • 0345222439 scopus 로고    scopus 로고
    • Dependence on the mobile phase pH of the adsorption behavior of propranolol enantiomers on a cellulase protein used as the chiral selector
    • Fornstedt T., Götmar G., Andersson M., Guiochon G. Dependence on the mobile phase pH of the adsorption behavior of propranolol enantiomers on a cellulase protein used as the chiral selector. J. Am. Chem. Soc. 121:1999;1164-1174.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 1164-1174
    • Fornstedt, T.1    Götmar, G.2    Andersson, M.3    Guiochon, G.4
  • 187
    • 0033965799 scopus 로고    scopus 로고
    • Chromatographic investigation on the binding site characteristic of quail egg-white riboflavin binding protein as a chiral stationary phase
    • Massolini G., De Lorenzi E., Calleri E., Tabolotti E., Caccialanza G. Chromatographic investigation on the binding site characteristic of quail egg-white riboflavin binding protein as a chiral stationary phase. J. Chromatogr. B. 738:2000;343-355.
    • (2000) J. Chromatogr. B , vol.738 , pp. 343-355
    • Massolini, G.1    De Lorenzi, E.2    Calleri, E.3    Tabolotti, E.4    Caccialanza, G.5
  • 188
    • 0034604801 scopus 로고    scopus 로고
    • Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein: VIII. Chiral recognition ability of partially and completely deglycosylated ovoglycoprotein
    • Haginaka J., Matsunaga H., Kakehi K. Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein: VIII. Chiral recognition ability of partially and completely deglycosylated ovoglycoprotein. J. Chromatogr. B. 745:2000;149-159.
    • (2000) J. Chromatogr. B , vol.745 , pp. 149-159
    • Haginaka, J.1    Matsunaga, H.2    Kakehi, K.3
  • 190
    • 0039178096 scopus 로고    scopus 로고
    • Retention mechanism of β-blockers on an immobilized cellulase. Relative importance of the hydrophobic and ionic contributions to their enantioselective and nonselective interactions
    • Götmar G., Fornstedt T., Guiochon G. Retention mechanism of β-blockers on an immobilized cellulase. Relative importance of the hydrophobic and ionic contributions to their enantioselective and nonselective interactions. Anal. Chem. 72:2000;3908-3915.
    • (2000) Anal. Chem. , vol.72 , pp. 3908-3915
    • Götmar, G.1    Fornstedt, T.2    Guiochon, G.3
  • 191
    • 0034634726 scopus 로고    scopus 로고
    • Cellobiohydrolase 58 (P.c. Cel 7D) is complementary to the homologous CBH I (T.r. Cel 7A) in enantioseparations
    • Henriksson H., Munoz I.G., Isaksson R., Pettersson G., Johansson G. Cellobiohydrolase 58 (P.c. Cel 7D) is complementary to the homologous CBH I (T.r. Cel 7A) in enantioseparations. J. Chromatogr. A. 898:2000;63-74.
    • (2000) J. Chromatogr. A , vol.898 , pp. 63-74
    • Henriksson, H.1    Munoz, I.G.2    Isaksson, R.3    Pettersson, G.4    Johansson, G.5
  • 192
    • 0032892811 scopus 로고    scopus 로고
    • Chitosan derivatives as chiral selectors bonded on allyl silica gel: Preparation, characterisation and study of the resulting high-performance liquid chromatography chiral stationary phases
    • Senso A., Oliveros L., Minguillón C. Chitosan derivatives as chiral selectors bonded on allyl silica gel: preparation, characterisation and study of the resulting high-performance liquid chromatography chiral stationary phases. J. Chromatogr. A. 839:1999;15-21.
    • (1999) J. Chromatogr. A , vol.839 , pp. 15-21
    • Senso, A.1    Oliveros, L.2    Minguillón, C.3
  • 193
    • 0033837476 scopus 로고    scopus 로고
    • Comparison of grafting modes for the preparation of cholic acid-based stationary phases. Influence on enantiomer separations in high-performance liquid chromatography
    • Vaton-Chanvrier L., Bucaille N., Combret Y., Combret J.-C. Comparison of grafting modes for the preparation of cholic acid-based stationary phases. Influence on enantiomer separations in high-performance liquid chromatography. J. Liq. Chromatogr. Relat. Technol. 23:2000;2155-2167.
    • (2000) J. Liq. Chromatogr. Relat. Technol. , vol.23 , pp. 2155-2167
    • Vaton-Chanvrier, L.1    Bucaille, N.2    Combret, Y.3    Combret, J.-C.4
  • 194
    • 0034016851 scopus 로고    scopus 로고
    • Uniform-sized molecularly imprinted polymer material for (S)-propranolol
    • Haginaka J., Sakai Y. Uniform-sized molecularly imprinted polymer material for (S)-propranolol. J. Pharm. Biomed. Anal. 22:2000;899-907.
    • (2000) J. Pharm. Biomed. Anal. , vol.22 , pp. 899-907
    • Haginaka, J.1    Sakai, Y.2
  • 196
    • 0034096033 scopus 로고    scopus 로고
    • Preparation and evaluation of the chiral stationary phases based on N-4-(2,5,6-trichloro-1,3-dicyano)-phenyl derivatives of L-α-amino acids
    • Kontrec D., Vinković V., Šunjić V. Preparation and evaluation of the chiral stationary phases based on N-4-(2,5,6-trichloro-1,3-dicyano)-phenyl derivatives of L-α-amino acids. J. Liq. Chromatogr. Relat. Technol. 23:2000;1203-1215.
    • (2000) J. Liq. Chromatogr. Relat. Technol. , vol.23 , pp. 1203-1215
    • Kontrec, D.1    Vinković, V.2    Šunjić, V.3
  • 197
    • 0034785695 scopus 로고    scopus 로고
    • Comparative study of the chiral resolution of beta-blockers on cellulose tris (3,5-dimethylphenylcarbamate) phases in normal and reversed phase modes
    • Schmid M.G., Gecse O., Szabo Z., Kilar F., Gübitz G., Ali I.et al. Comparative study of the chiral resolution of beta-blockers on cellulose tris (3,5-dimethylphenylcarbamate) phases in normal and reversed phase modes. J. Liq. Chromatogr. Relat. Technol. 24:2001;2493-2504.
    • (2001) J. Liq. Chromatogr. Relat. Technol. , vol.24 , pp. 2493-2504
    • Schmid, M.G.1    Gecse, O.2    Szabo, Z.3    Kilar, F.4    Gübitz, G.5    Ali, I.6
  • 198
  • 199
    • 0033199545 scopus 로고    scopus 로고
    • Riboflavin binding proteins as chiral selectors in HPLC and CE
    • De Lorenzi E., Massolini G. Riboflavin binding proteins as chiral selectors in HPLC and CE. Pharm. Sci. Technol. Today. 2:1999;352-364.
    • (1999) Pharm. Sci. Technol. Today , vol.2 , pp. 352-364
    • De Lorenzi, E.1    Massolini, G.2
  • 200
    • 0035847188 scopus 로고    scopus 로고
    • Reversed-phase liquid chromatographic separation of enantiomers on polysaccharide type chiral stationary phases
    • Tachibana K., Ohnishi A. Reversed-phase liquid chromatographic separation of enantiomers on polysaccharide type chiral stationary phases. J. Chromatogr. A. 906:2001;127-154.
    • (2001) J. Chromatogr. A , vol.906 , pp. 127-154
    • Tachibana, K.1    Ohnishi, A.2
  • 201
    • 0035847234 scopus 로고    scopus 로고
    • Regioselectively modified polysaccharide derivatives as chiral stationary phases in high-performance liquid chromatography
    • Felix G. Regioselectively modified polysaccharide derivatives as chiral stationary phases in high-performance liquid chromatography. J. Chromatogr. A. 906:2001;171-184.
    • (2001) J. Chromatogr. A , vol.906 , pp. 171-184
    • Felix, G.1
  • 202
    • 0035847212 scopus 로고    scopus 로고
    • High-performance liquid chromatographic enantioseparation of drugs containing multiple chiral centers on polysaccharide-type chiral stationary phases
    • Aboul-Enein H.Y. High-performance liquid chromatographic enantioseparation of drugs containing multiple chiral centers on polysaccharide-type chiral stationary phases. J. Chromatogr. A. 906:2001;185-193.
    • (2001) J. Chromatogr. A , vol.906 , pp. 185-193
    • Aboul-Enein, H.Y.1
  • 203
    • 0030682510 scopus 로고    scopus 로고
    • Enantiomeric separation of amino alcohols using Z-L-Glu-L-Pro or Z-L-Glu-D-Pro as a chiral counter ions and hypercarb as the solid phase
    • Karlsson A., Karlsson O. Enantiomeric separation of amino alcohols using Z-L-Glu-L-Pro or Z-L-Glu-D-Pro as a chiral counter ions and hypercarb as the solid phase. Chirality. 9:1997;650-655.
    • (1997) Chirality , vol.9 , pp. 650-655
    • Karlsson, A.1    Karlsson, O.2
  • 204
    • 0032919499 scopus 로고    scopus 로고
    • Direct high-performance liquid chromatographic separations of metoprolol analogues on a Chiralcel OD column using chemometrics
    • Svensson S., Vessman J., Karlsson A. Direct high-performance liquid chromatographic separations of metoprolol analogues on a Chiralcel OD column using chemometrics. J. Chromatogr. A. 839:1999;23-39.
    • (1999) J. Chromatogr. A , vol.839 , pp. 23-39
    • Svensson, S.1    Vessman, J.2    Karlsson, A.3
  • 205
    • 0032784141 scopus 로고    scopus 로고
    • Use of immobilized amyloglucosidase as chiral selector in chromatography. Immobilization and performance in liquid chromatography
    • Nyström A., Strandberg A., Aspegren A., Behr S., Karlsson A. Use of immobilized amyloglucosidase as chiral selector in chromatography. Immobilization and performance in liquid chromatography. Chromatographia. 50:1999;209-214.
    • (1999) Chromatographia , vol.50 , pp. 209-214
    • Nyström, A.1    Strandberg, A.2    Aspegren, A.3    Behr, S.4    Karlsson, A.5
  • 206
    • 0032766257 scopus 로고    scopus 로고
    • Use of immobilized amyloglucosidase as chiral selector in chromatography. Control of enantioselective retention and resolution in liquid chromatography
    • Strandberg A., Nyström A., Behr S., Karlsson A. Use of immobilized amyloglucosidase as chiral selector in chromatography. Control of enantioselective retention and resolution in liquid chromatography. Chromatographia. 50:1999;215-222.
    • (1999) Chromatographia , vol.50 , pp. 215-222
    • Strandberg, A.1    Nyström, A.2    Behr, S.3    Karlsson, A.4
  • 207
    • 0033988322 scopus 로고    scopus 로고
    • Enantiomeric separation of amino alcohols on protein phases using statistical experimental desing. A comparative study
    • Karlsson A., Aspegren A. Enantiomeric separation of amino alcohols on protein phases using statistical experimental desing. A comparative study. J. Chromatogr. A. 866:2000;15-23.
    • (2000) J. Chromatogr. A , vol.866 , pp. 15-23
    • Karlsson, A.1    Aspegren, A.2
  • 208
    • 0034024085 scopus 로고    scopus 로고
    • Chiral separation of metoprolol and some analogs with carbon dioxide on Chiralcel OD and Chiralpak AD stationary phases. Use of chemometrics
    • Svensson S., Karlsson A., Gyllenhaal O., Vessman J. Chiral separation of metoprolol and some analogs with carbon dioxide on Chiralcel OD and Chiralpak AD stationary phases. Use of chemometrics. Chromatographia. 51:2000;283-293.
    • (2000) Chromatographia , vol.51 , pp. 283-293
    • Svensson, S.1    Karlsson, A.2    Gyllenhaal, O.3    Vessman, J.4
  • 209
    • 0035808707 scopus 로고    scopus 로고
    • Chiral ion-pair chromatography on porous graphitized carbon using N-blocked dipeptides as counter ions
    • Karlsson A., Karlsson O. Chiral ion-pair chromatography on porous graphitized carbon using N-blocked dipeptides as counter ions. J. Chromatogr. A. 905:2001;329-335.
    • (2001) J. Chromatogr. A , vol.905 , pp. 329-335
    • Karlsson, A.1    Karlsson, O.2
  • 210
    • 0031008496 scopus 로고    scopus 로고
    • Separation of enantiomers of 4-aryldihydropyrimidines by direct enantioselective HPLC. A critical comparison of chiral stationary phases
    • Kleidernigg O.P., Kappe C.O. Separation of enantiomers of 4-aryldihydropyrimidines by direct enantioselective HPLC. A critical comparison of chiral stationary phases. Tetrahedron: Asymmetry. 8:1997;2057-2067.
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 2057-2067
    • Kleidernigg, O.P.1    Kappe, C.O.2
  • 211
    • 0344500793 scopus 로고    scopus 로고
    • Separation of enantiomers of some 1,4-piperazine derivatives of aryloxyaminopropanols on a vancomycin chiral stationary phase
    • Lehotay J., Hroboňová K., Cižmárik J., Celková H. Separation of enantiomers of some 1,4-piperazine derivatives of aryloxyaminopropanols on a vancomycin chiral stationary phase. Pharmazie. 54:1999;743-745.
    • (1999) Pharmazie , vol.54 , pp. 743-745
    • Lehotay, J.1    Hroboňová, K.2    Cižmárik, J.3    Celková, H.4
  • 212
    • 0034837256 scopus 로고    scopus 로고
    • Study of the mechanism of enantioseparation: I. Chiral analysis of alkylamino derivatives of aryloxypropanols by HPLC using macrocyclic antibiotics as chiral selectors
    • Hroboňová K., Lehotay J., Cižmáriková J., Armstrong D.W. Study of the mechanism of enantioseparation: I. Chiral analysis of alkylamino derivatives of aryloxypropanols by HPLC using macrocyclic antibiotics as chiral selectors. J. Liq. Chromatogr. Relat. Technol. 24:2001;2225-2237.
    • (2001) J. Liq. Chromatogr. Relat. Technol. , vol.24 , pp. 2225-2237
    • Hroboňová, K.1    Lehotay, J.2    Cižmáriková, J.3    Armstrong, D.W.4
  • 213
    • 0035094628 scopus 로고    scopus 로고
    • HPLC enantiomeric resolution of nebivolol on normal and reversed amylose based chiral phases
    • Aboul-Enein H.Y., Ali I. HPLC enantiomeric resolution of nebivolol on normal and reversed amylose based chiral phases. Pharmazie. 56:2001;214-216.
    • (2001) Pharmazie , vol.56 , pp. 214-216
    • Aboul-Enein, H.Y.1    Ali, I.2
  • 214
    • 0034944319 scopus 로고    scopus 로고
    • Chiral separation of verapamil and some of its metabolites by HPLC and CE
    • Brandšteterova E., Endresz G., Blaschke G. Chiral separation of verapamil and some of its metabolites by HPLC and CE. Pharmazie. 56:2001;536-541.
    • (2001) Pharmazie , vol.56 , pp. 536-541
    • Brandšteterova, E.1    Endresz, G.2    Blaschke, G.3
  • 215
    • 0034123933 scopus 로고    scopus 로고
    • Enantiomer separation of pharmaceuticals by capillary gas chromatography with novel chiral stationary phases
    • Abe I., Terada K., Nakahara T. Enantiomer separation of pharmaceuticals by capillary gas chromatography with novel chiral stationary phases. Biomed. Chromatogr. 14:2000;125-129.
    • (2000) Biomed. Chromatogr. , vol.14 , pp. 125-129
    • Abe, I.1    Terada, K.2    Nakahara, T.3
  • 216
    • 0030851895 scopus 로고    scopus 로고
    • Bioequivalence of chiral drugs
    • Mehvar R., Jamali F. Bioequivalence of chiral drugs. Clin. Pharmacokinet. 33:1997;122-141.
    • (1997) Clin. Pharmacokinet. , vol.33 , pp. 122-141
    • Mehvar, R.1    Jamali, F.2
  • 217
    • 0030774486 scopus 로고    scopus 로고
    • Time to reassess chiral aspects of β-adrenoceptor antagonists
    • Stoschitzky K., Lindner W. Time to reassess chiral aspects of β-adrenoceptor antagonists. Trends Pharmacol. Sci. 18:1997;306-307.
    • (1997) Trends Pharmacol. Sci. , vol.18 , pp. 306-307
    • Stoschitzky, K.1    Lindner, W.2
  • 218
    • 0033127928 scopus 로고    scopus 로고
    • 2-adrenoceptor agonists: Is there a cause for concern?
    • 2-adrenoceptor agonists: is there a cause for concern? J. Allergy Clin. Immunol. 103:1999;742-748.
    • (1999) J. Allergy Clin. Immunol. , vol.103 , pp. 742-748
    • Waldeck, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.