메뉴 건너뛰기




Volumn 1467, Issue , 2016, Pages 297-305

Separation and elution order of the enantiomers of some β-agonists using polysaccharide-based chiral columns and normal phase eluents by high-performance liquid chromatography

Author keywords

Beta agonist; Enantiomer elution order; Enantioseparations; HPLC; Mobile phase additives; Polysaccharide based chiral columns

Indexed keywords

CHROMATOGRAPHY; ENANTIOMERS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROCARBONS; LIQUID CHROMATOGRAPHY; SEPARATION;

EID: 84991051983     PISSN: 00219673     EISSN: 18733778     Source Type: Journal    
DOI: 10.1016/j.chroma.2016.08.011     Document Type: Article
Times cited : (25)

References (36)
  • 1
    • 0000217817 scopus 로고    scopus 로고
    • Catecholamines, sympathomimetic drugs, and adrenergic receptor antagonists
    • J.G. Hardman L.E. Limbird 9th ed. McGraw Hill New York
    • [1] Hoffman, B.B., Lefkowitz, R.J., Catecholamines, sympathomimetic drugs, and adrenergic receptor antagonists. Hardman, J.G., Limbird, L.E., (eds.) The Pharmacologic Basis of Therapeutics, 9th ed., 1996, McGraw Hill, New York, 199–248.
    • (1996) The Pharmacologic Basis of Therapeutics , pp. 199-248
    • Hoffman, B.B.1    Lefkowitz, R.J.2
  • 3
    • 33947325045 scopus 로고    scopus 로고
    • Treatment with (R)-albuterol has no advantage over racemic albuterol
    • [3] Barnes, P.J., Treatment with (R)-albuterol has no advantage over racemic albuterol. Am. J. Resp. Crit. Care Med. 174 (2006), 969–972.
    • (2006) Am. J. Resp. Crit. Care Med. , vol.174 , pp. 969-972
    • Barnes, P.J.1
  • 4
    • 33749341128 scopus 로고    scopus 로고
    • Opposing actions of (R,R)-isomers and (S,S)-isomers of formoterol on T-cell function
    • [4] Steinke, J.W., Baramki, D., Borish, L., Opposing actions of (R,R)-isomers and (S,S)-isomers of formoterol on T-cell function. J. Allergy Clin. Immunol. 118 (2006), 963–965.
    • (2006) J. Allergy Clin. Immunol. , vol.118 , pp. 963-965
    • Steinke, J.W.1    Baramki, D.2    Borish, L.3
  • 5
    • 0003808170 scopus 로고    scopus 로고
    • Capillary Electrophoresis in Chiral Analysis
    • Wiley&Sons Chichester pp. 555
    • [5] Chankvetadze, B., Capillary Electrophoresis in Chiral Analysis. 1997, Wiley&Sons, Chichester pp. 555.
    • (1997)
    • Chankvetadze, B.1
  • 6
    • 0002789966 scopus 로고
    • Eluting trace components before major constituents: I. Sensitivity enhancement in analytical determinations of optical purity
    • [6] Perry, J.A., Rateike, J.D., Szczerba, T.J., Eluting trace components before major constituents: I. Sensitivity enhancement in analytical determinations of optical purity. J. Chromatogr. A 389 (1987), 57–64.
    • (1987) J. Chromatogr. A , vol.389 , pp. 57-64
    • Perry, J.A.1    Rateike, J.D.2    Szczerba, T.J.3
  • 7
    • 84872110591 scopus 로고    scopus 로고
    • HPLC separation of enantiomers of chiral arylpropionic acid derivatives using polysaccharide-based chiral columns and normal-phase eluents with emphasis on elution order
    • [7] Matarashvili, I., Chankvetadze, L., Fanali, S., Farkas, T., Chankvetadze, B., HPLC separation of enantiomers of chiral arylpropionic acid derivatives using polysaccharide-based chiral columns and normal-phase eluents with emphasis on elution order. J. Sep. Sci. 36 (2013), 140–147.
    • (2013) J. Sep. Sci. , vol.36 , pp. 140-147
    • Matarashvili, I.1    Chankvetadze, L.2    Fanali, S.3    Farkas, T.4    Chankvetadze, B.5
  • 8
    • 0026570670 scopus 로고
    • Reversed retention order and other stereoselective effects in the separation of amino alcohols on Chiralcel OD
    • [8] Balmer, K., Lagerström, P.-O., Persson, B.-A., Schill, G., Reversed retention order and other stereoselective effects in the separation of amino alcohols on Chiralcel OD. J. Chromatogr. A 592 (1992), 331–337.
    • (1992) J. Chromatogr. A , vol.592 , pp. 331-337
    • Balmer, K.1    Lagerström, P.-O.2    Persson, B.-A.3    Schill, G.4
  • 9
    • 84866704376 scopus 로고    scopus 로고
    • HPLC separation of dihydropyridine derivatives enantiomers with emphasis on elution order using polysaccharide-based chiral columns
    • [9] Jibuti, G., Mskhiladze, A., Takaishvili, N., Karchkhadze, M., Chankvetadze, L., Farkas, T., Chankvetadze, B., HPLC separation of dihydropyridine derivatives enantiomers with emphasis on elution order using polysaccharide-based chiral columns. J. Sep. Sci. 35 (2012), 2529–2537.
    • (2012) J. Sep. Sci. , vol.35 , pp. 2529-2537
    • Jibuti, G.1    Mskhiladze, A.2    Takaishvili, N.3    Karchkhadze, M.4    Chankvetadze, L.5    Farkas, T.6    Chankvetadze, B.7
  • 10
    • 79960826096 scopus 로고    scopus 로고
    • Determination of enantiomeric purity of S-amlodipine by chiral LC with emphasis on reversal of enantiomer elution order
    • [10] Dossou, K.S.S., Edorh, P.A., Chiap, P., Chankvetadze, B., Servais, A.-C., Fillet, M., Crommen, J., Determination of enantiomeric purity of S-amlodipine by chiral LC with emphasis on reversal of enantiomer elution order. J. Sep. Sci. 34 (2011), 1772–1780.
    • (2011) J. Sep. Sci. , vol.34 , pp. 1772-1780
    • Dossou, K.S.S.1    Edorh, P.A.2    Chiap, P.3    Chankvetadze, B.4    Servais, A.-C.5    Fillet, M.6    Crommen, J.7
  • 11
    • 0035943465 scopus 로고    scopus 로고
    • Effect of mobile phase acidic additives on enantioselectivity for phenylalanine analogs
    • [11] Ye, Y.K., Stringham, R.W., Effect of mobile phase acidic additives on enantioselectivity for phenylalanine analogs. J. Chromatogr. A 927 (2001), 47–52.
    • (2001) J. Chromatogr. A , vol.927 , pp. 47-52
    • Ye, Y.K.1    Stringham, R.W.2
  • 12
    • 15744380498 scopus 로고    scopus 로고
    • Chiral separation of amines in subcritical fluid chromatography using polysaccharide stationary phases and acidic additives
    • [12] Stringham, R.W., Chiral separation of amines in subcritical fluid chromatography using polysaccharide stationary phases and acidic additives. J. Chromatogr. A 1070 (2005), 163–170.
    • (2005) J. Chromatogr. A , vol.1070 , pp. 163-170
    • Stringham, R.W.1
  • 13
    • 0030176327 scopus 로고    scopus 로고
    • High performance liquid chromatography enantioseparation of chiral pharmaceuticals using tris(chloro-methylphenylcarbamate)s of cellulose
    • [13] Chankvetadze, B., Chankvetadze, L., Sidamonidze, Sh., Yashima, E., Okamoto, Y., High performance liquid chromatography enantioseparation of chiral pharmaceuticals using tris(chloro-methylphenylcarbamate)s of cellulose. J. Pharm. Biomed. Anal. 14 (1996), 1295–1303.
    • (1996) J. Pharm. Biomed. Anal. , vol.14 , pp. 1295-1303
    • Chankvetadze, B.1    Chankvetadze, L.2    Sidamonidze, S.3    Yashima, E.4    Okamoto, Y.5
  • 14
    • 56449100061 scopus 로고    scopus 로고
    • Synergistic effects on enantioselectivity of zwitterionic chiral stationary phases for separations of chiral acids bases, and amino acids by HPLC
    • [14] Hoffmann, C.V., Pell, R., Lämmerhofer, M., Lindner, W., Synergistic effects on enantioselectivity of zwitterionic chiral stationary phases for separations of chiral acids bases, and amino acids by HPLC. Anal. Chem. 80 (2008), 8780–8789.
    • (2008) Anal. Chem. , vol.80 , pp. 8780-8789
    • Hoffmann, C.V.1    Pell, R.2    Lämmerhofer, M.3    Lindner, W.4
  • 15
    • 84929841402 scopus 로고    scopus 로고
    • Enantioseparations of 11 amino alcohols Using di-n-amyl l-tartrate–boric acid complex as chiral mobile phase additive by RP-HPLC
    • [15] Zou, Y., Wang, L., Liu, Q., Liu, H., Li, F., Enantioseparations of 11 amino alcohols Using di-n-amyl l-tartrate–boric acid complex as chiral mobile phase additive by RP-HPLC. Chromatographia 78 (2015), 753–761.
    • (2015) Chromatographia , vol.78 , pp. 753-761
    • Zou, Y.1    Wang, L.2    Liu, Q.3    Liu, H.4    Li, F.5
  • 16
    • 84941738274 scopus 로고    scopus 로고
    • Enantioseparation tuned by solvent polarity on a β-cyclodextrin clicked chiral stationary phase
    • [16] Tang, J., Pang, L., Zhou, J., Tang, W., Enantioseparation tuned by solvent polarity on a β-cyclodextrin clicked chiral stationary phase. J. Sep. Sci. 38 (2015), 3137–3144.
    • (2015) J. Sep. Sci. , vol.38 , pp. 3137-3144
    • Tang, J.1    Pang, L.2    Zhou, J.3    Tang, W.4
  • 17
    • 0036027739 scopus 로고    scopus 로고
    • Enantioseparation of chiral vasodilator drug isoxsuprine in high-performance liquid chromatography and capillary electrophoresis
    • [17] Chankvetadze, B., Burjanadze, N., Blaschke, G., Enantioseparation of chiral vasodilator drug isoxsuprine in high-performance liquid chromatography and capillary electrophoresis. J. Pharm. Biomed. Anal. 27 (2002), 153–159.
    • (2002) J. Pharm. Biomed. Anal. , vol.27 , pp. 153-159
    • Chankvetadze, B.1    Burjanadze, N.2    Blaschke, G.3
  • 19
    • 84866253088 scopus 로고    scopus 로고
    • Comparison of separation performances of novel β-cyclodextrin-based chiral stationary phases in high-performance liquid chromatographic enantioseparation
    • [19] Varga, G., Fodor, G., Ilisz, I., Szemán, J., Visy, J., Szente, L., Péter, A., Comparison of separation performances of novel β-cyclodextrin-based chiral stationary phases in high-performance liquid chromatographic enantioseparation. J. Pharm. Biomed. Anal. 70 (2012), 71–76.
    • (2012) J. Pharm. Biomed. Anal. , vol.70 , pp. 71-76
    • Varga, G.1    Fodor, G.2    Ilisz, I.3    Szemán, J.4    Visy, J.5    Szente, L.6    Péter, A.7
  • 20
    • 80052103715 scopus 로고    scopus 로고
    • Effect of chromatographic conditions on liquid chromatographic chiral separation of terbutaline and salbutamol on Chirobiotic V column
    • [20] Hashem, H., Tründelberg, C., Attef, O., Jira, T., Effect of chromatographic conditions on liquid chromatographic chiral separation of terbutaline and salbutamol on Chirobiotic V column. J. Chromatogr. A 1218 (2011), 6727–6731.
    • (2011) J. Chromatogr. A , vol.1218 , pp. 6727-6731
    • Hashem, H.1    Tründelberg, C.2    Attef, O.3    Jira, T.4
  • 21
    • 33745372935 scopus 로고    scopus 로고
    • The effect of acidic and basic additives on the enantioseparation of basic drugs using polysaccharide-based chiral stationary phases
    • [21] Ye, Y.K., Stringham, R.W., The effect of acidic and basic additives on the enantioseparation of basic drugs using polysaccharide-based chiral stationary phases. Chirality 18 (2006), 519–530.
    • (2006) Chirality , vol.18 , pp. 519-530
    • Ye, Y.K.1    Stringham, R.W.2
  • 22
    • 77349119362 scopus 로고    scopus 로고
    • Simultaneous analysis of bambuterol and its active metabolite terbutaline enantiomers in rat plasma by chiral liquid chromatography-tandem mass spectrometry
    • [22] Luo, W., Zhu, L., Deng, J., Liu, A., Guo, B., Tan, W., Dai, R., Simultaneous analysis of bambuterol and its active metabolite terbutaline enantiomers in rat plasma by chiral liquid chromatography-tandem mass spectrometry. J. Pharm. Biomed. Anal. 52 (2010), 227–231.
    • (2010) J. Pharm. Biomed. Anal. , vol.52 , pp. 227-231
    • Luo, W.1    Zhu, L.2    Deng, J.3    Liu, A.4    Guo, B.5    Tan, W.6    Dai, R.7
  • 23
    • 0035085769 scopus 로고    scopus 로고
    • High-performance liquid chromatographic and capillary electrophoretic methods for the quantitation of the (S)-terbutaline in (R)-terbutaline
    • [23] 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
  • 24
    • 0037467098 scopus 로고    scopus 로고
    • Direct separation and quantitative determination of clenbuterol enantiomers by high performance liquid chromatography using an amide type chiral stationary phase
    • [24] Song, Y., Wang, D., Hu, Y., Chen, X., Jiao, Y., Hou, D., Direct separation and quantitative determination of clenbuterol enantiomers by high performance liquid chromatography using an amide type chiral stationary phase. J. Pharm. Biomed. Anal. 31 (2003), 311–319.
    • (2003) J. Pharm. Biomed. Anal. , vol.31 , pp. 311-319
    • Song, Y.1    Wang, D.2    Hu, Y.3    Chen, X.4    Jiao, Y.5    Hou, D.6
  • 25
    • 0029923463 scopus 로고    scopus 로고
    • Direct enantioselective separation of clenbuterol by chiral HPLC in biological fluids
    • [25] Abou-Basha, L.I., Aboul-Enein, H.Y., Direct enantioselective separation of clenbuterol by chiral HPLC in biological fluids. Biomed. Chromatogr. 10 (1996), 69–72.
    • (1996) Biomed. Chromatogr. , vol.10 , pp. 69-72
    • Abou-Basha, L.I.1    Aboul-Enein, H.Y.2
  • 26
    • 84887196510 scopus 로고    scopus 로고
    • Strong cation exchange chiral stationary phase—A comparative study in high-performance liquid chromatography and subcritical fluid chromatography
    • [26] Wolrab, D., Macíková, P., Boras, M., Kohout, M., Lindner, W., Strong cation exchange chiral stationary phase—A comparative study in high-performance liquid chromatography and subcritical fluid chromatography. J. Chromatogr. A 1317 (2013), 59–66.
    • (2013) J. Chromatogr. A , vol.1317 , pp. 59-66
    • Wolrab, D.1    Macíková, P.2    Boras, M.3    Kohout, M.4    Lindner, W.5
  • 27
    • 33646538426 scopus 로고    scopus 로고
    • On the use of dispersed nanoparticles modified with single layer β-cyclodextrin as chiral selecor to enhance enantioseparation of clenbuterol with capillary electrophoresis
    • [27] Na, N., Hu, Y., Ouyang, J., Baeyens, W.R.G., Delanghe, J.R., Taes, Y.E.C., Xie, M., Chen, H., Yang, Y., On the use of dispersed nanoparticles modified with single layer β-cyclodextrin as chiral selecor to enhance enantioseparation of clenbuterol with capillary electrophoresis. Talanta 69 (2006), 866–872.
    • (2006) Talanta , vol.69 , pp. 866-872
    • Na, N.1    Hu, Y.2    Ouyang, J.3    Baeyens, W.R.G.4    Delanghe, J.R.5    Taes, Y.E.C.6    Xie, M.7    Chen, H.8    Yang, Y.9
  • 28
    • 51049100199 scopus 로고    scopus 로고
    • Effects of alcohols on CE enantioseparation of basic drugs with native γ-CD as chiral selector
    • [28] Deñola, N.L., Quiming, N.S., Catabay, A.P., Saito, Y., Jinno, K., Effects of alcohols on CE enantioseparation of basic drugs with native γ-CD as chiral selector. J. Sep. Sci. 31 (2008), 2701–2706.
    • (2008) J. Sep. Sci. , vol.31 , pp. 2701-2706
    • Deñola, N.L.1    Quiming, N.S.2    Catabay, A.P.3    Saito, Y.4    Jinno, K.5
  • 29
    • 84863164025 scopus 로고    scopus 로고
    • Enantioseparation of β-agonists with carboxymethyl-β-cyclodextrin by CE
    • [29] Zhou, J., Yao, H., Shao, H., Li, Y., Zhang, Z., Enantioseparation of β-agonists with carboxymethyl-β-cyclodextrin by CE. J. Liq. Chromatogr. Relat. Technol. 35 (2012), 50–58.
    • (2012) J. Liq. Chromatogr. Relat. Technol. , vol.35 , pp. 50-58
    • Zhou, J.1    Yao, H.2    Shao, H.3    Li, Y.4    Zhang, Z.5
  • 30
    • 84916595326 scopus 로고    scopus 로고
    • Capillary electrochromatographic fast enantioseparation based on a chiral metal?organic framework
    • [30] Fei, Z.-X., Zhang, M., Xie, S.-M., Yuan, L.-M., Capillary electrochromatographic fast enantioseparation based on a chiral metal?organic framework. Electrophoresis 35 (2014), 3541–3548.
    • (2014) Electrophoresis , vol.35 , pp. 3541-3548
    • Fei, Z.-X.1    Zhang, M.2    Xie, S.-M.3    Yuan, L.-M.4
  • 31
    • 77954621576 scopus 로고    scopus 로고
    • Click immobilized perphenylcarbamated and permethylated cyclodextrin stationary phases for chiral high-performance liquid chromatography application
    • [31] Wang, Y., Young, D.J., Tan, T.T.Y., Ng, S.-C., Click immobilized perphenylcarbamated and permethylated cyclodextrin stationary phases for chiral high-performance liquid chromatography application. J. Chromatogr. A 1217 (2010), 5103–5108.
    • (2010) J. Chromatogr. A , vol.1217 , pp. 5103-5108
    • Wang, Y.1    Young, D.J.2    Tan, T.T.Y.3    Ng, S.-C.4
  • 32
    • 84870315859 scopus 로고    scopus 로고
    • Recent developments on polysaccharide-based chiral stationary phases for liquid-phase separation of enantiomers
    • [32] Chankvetadze, B., Recent developments on polysaccharide-based chiral stationary phases for liquid-phase separation of enantiomers. J. Chromatogr. A 1269 (2012), 26–51.
    • (2012) J. Chromatogr. A , vol.1269 , pp. 26-51
    • Chankvetadze, B.1
  • 33
    • 84924061954 scopus 로고    scopus 로고
    • Effect of basic and acidic additives on the separation of some basic drug enantiomers on polysaccharide-based chiral columns with acetonitrile as mobile phase
    • [33] Gogaladze, K., Chankvetadze, L., Tsintsadze, M., Farkas, T., Chankvetadze, B., Effect of basic and acidic additives on the separation of some basic drug enantiomers on polysaccharide-based chiral columns with acetonitrile as mobile phase. Chirality 27 (2015), 228–234.
    • (2015) Chirality , vol.27 , pp. 228-234
    • Gogaladze, K.1    Chankvetadze, L.2    Tsintsadze, M.3    Farkas, T.4    Chankvetadze, B.5
  • 34
    • 84887159777 scopus 로고    scopus 로고
    • On the effect of basic and acidic additives on the separation of the enantiomers of some basic drugs with polysaccharide-based chiral selectors and polar organic mobile phases
    • [34] Mosiashvili, L., Chankvetadze, L., Farkas, T., Chankvetadze, B., On the effect of basic and acidic additives on the separation of the enantiomers of some basic drugs with polysaccharide-based chiral selectors and polar organic mobile phases. J. Chromatogr A 1317 (2013), 167–174.
    • (2013) J. Chromatogr A , vol.1317 , pp. 167-174
    • Mosiashvili, L.1    Chankvetadze, L.2    Farkas, T.3    Chankvetadze, B.4
  • 35
    • 84904747309 scopus 로고    scopus 로고
    • Enantioseparation of selected chiral sulfoxides in high-performance liquid chromatography with polysaccharide-based chiral selectors in polar organic mobile phases with emphasis on enantiomer elution order
    • [35] Gegenava, M., Chankvetadze, L., Farkas, T., Chankvetadze, B., Enantioseparation of selected chiral sulfoxides in high-performance liquid chromatography with polysaccharide-based chiral selectors in polar organic mobile phases with emphasis on enantiomer elution order. J. Sep. Sci. 37 (2014), 1083–1088.
    • (2014) J. Sep. Sci. , vol.37 , pp. 1083-1088
    • Gegenava, M.1    Chankvetadze, L.2    Farkas, T.3    Chankvetadze, B.4
  • 36
    • 80051888226 scopus 로고    scopus 로고
    • Enantiomer elution order reversal of fluorenylmethoxycarbonyl-isoleucine in high-performance liquid chromatography by changing the mobile phase temperature and composition
    • [36] Chankvetadze, L., Ghibradze, N., Karchkhadze, M., Peng, L., Farkas, T., Chankvetadze, B., Enantiomer elution order reversal of fluorenylmethoxycarbonyl-isoleucine in high-performance liquid chromatography by changing the mobile phase temperature and composition. J. Chromatogr. A 1218 (2011), 6554–6560.
    • (2011) J. Chromatogr. A , vol.1218 , pp. 6554-6560
    • Chankvetadze, L.1    Ghibradze, N.2    Karchkhadze, M.3    Peng, L.4    Farkas, T.5    Chankvetadze, B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.