Literature DB >> 10821402

Chromatographic separation of chlorthalidone enantiomers using beta-cyclodextrins as chiral additives.

R Herráez-Hernández1, P Campíns-Falcó.   

Abstract

Different beta-cyclodextrins have been tested as chiral additives in the mobile phase for the chromatographic analysis of chlorthalidone enantiomers in a C18 LiChrospher (125 x 4 mm I.D.) column. The effect on enantioresolution of different parameters was studied: composition of the mobile phase (percentage of organic solvent, type of buffer and pH), mobile phase flow-rate, and type and concentration of beta-cyclodextrin. A 25:75 mixture of methanol and 0.1 M phosphate buffer, pH 4, containing 2% triethylamine (v/v), and 12.5 mM beta-cyclodextrin, at a flow-rate of 0.8 ml/min, was found to be the best option for the resolution of chlorthalidone enantiomers. Under such conditions, linear calibration curves were obtained in the 0.5-20-microg/ml interval using UV detection at 230 nm. The limit of detection for both isomers was 50 ng/ml. The utility of the described assay has been tested by analyzing chlorthalidone in different pharmaceutical preparations. Examples of application to biological samples are also given.

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Year:  2000        PMID: 10821402     DOI: 10.1016/s0378-4347(00)00103-1

Source DB:  PubMed          Journal:  J Chromatogr B Biomed Sci Appl        ISSN: 1387-2273


  1 in total

1.  Enantioseparation of mandelic acid derivatives by high performance liquid chromatography with substituted β-cyclodextrin as chiral mobile phase additive and evaluation of inclusion complex formation.

Authors:  Shengqiang Tong; Hu Zhang; Mangmang Shen; Yoichiro Ito; Jizhong Yan
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2014-05-22       Impact factor: 3.205

  1 in total

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