Analysis of repaglinide enantiomers in pharmaceutical formulations by capillary electrophoresis using 2,6-di-o-methyl-β-cyclodextrin as a chiral selector

Journal of Chromatographic Science

Volumn 50, Issue 8, 2012, Pages 739-743

  Li, Cen ^a   Jiang, Ye ^a  

^a HEBEI MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

2,6 O DIMETHYL BETA CYCLODEXTRIN; 2,6-DI-O-METHYL-BETA-CYCLODEXTRIN; BETA CYCLODEXTRIN DERIVATIVE; CARBAMIC ACID DERIVATIVE; PIPERIDINE DERIVATIVE; REPAGLINIDE;

ARTICLE; CAPILLARY ELECTROPHORESIS; CHEMISTRY; DRUG CONTAMINATION; LIMIT OF DETECTION; METHODOLOGY; PH; REPRODUCIBILITY; STATISTICAL MODEL; STEREOISOMERISM; TABLET;

BETA-CYCLODEXTRINS; CARBAMATES; DRUG CONTAMINATION; ELECTROPHORESIS, CAPILLARY; HYDROGEN-ION CONCENTRATION; LIMIT OF DETECTION; LINEAR MODELS; PIPERIDINES; REPRODUCIBILITY OF RESULTS; STEREOISOMERISM; TABLETS;

EID: 84866327288     PISSN: 00219665     EISSN: None     Source Type: Journal    
DOI: 10.1093/chromsci/bms064     Document Type: Article

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