4.6 Article

Preparative enantioseparation of β-blocker drugs by counter-current chromatography using dialkyl L-tartrate as chiral selector based on borate coordination complex

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1263, Issue -, Pages 74-83

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2012.09.023

Keywords

Preparative enantioseparation; Counter-current chromatography; pH-zone-refining mode; Di-n-hexyl L-tartrate; Borate coordination complex; beta-Blocker drugs

Funding

  1. National Natural Science Foundation of China [21105090]
  2. Natural Science Foundation of Zhejiang Province, China [Y4100472]
  3. Science and Technology Department of Zhejiang Province, China [2010C33144]

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Counter-current chromatography (CCC) was applied for preparative enantioseparation of three beta-blocker drugs, including propranolol, pindolol and alprenolol. The two-phase solvent system was composed of chloroform-0.05 mol L-1 acetate buffer containing 0.10 mol L-1 boricacid (1:1, v/v), in which 0.10 mol L-1 di-n-hexyl L-tartrate was added in the organic phase as chiral selector. Influence factors in the enantioseparation of propranolol were investigated. The chromatographic retention mechanism based on borate coordination complex was proposed. 116 mg of racemic propranolol was completely enantioseparated using conventional high speed CCC in a single run, yielding 48 mg of (+)-propranolol with HPLC purity of 98.9% and 47 mg of (-)-propranolol with HPLC purity of 96.3%. Recovery for propranolol enantiomers from CCC fractions was in the range of 75-82%. pH-zone-refining CCC was also successfully applied in enantioseparation of propanolol and it was found that 356 mg of racemic propranolol could be completely enantioseparated. 145 mg of (+)-enantiomer with HPLC purity of 95.6% and 148 mg of (-)-enantiomer with HPLC purity of 98.2% were recovered from pH-zone-refining mode. Separation mechanism about chiral separation by pH-zone-refining CCC was discussed. (C) 2012 Elsevier B.V. All rights reserved.

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