ANALYSIS OF ANTHRAQUINONE SULFONATES - COMPARISON OF CAPILLARY ELECTROPHORESIS WITH HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY

被引:44
作者
WILLIAMS, SJ
GOODALL, DM
EVANS, KP
机构
[1] UNIV YORK,DEPT CHEM,YORK YO1 5DD,N YORKSHIRE,ENGLAND
[2] ICI SPECIALITIES,MANCHESTER M9 3DA,ENGLAND
来源
JOURNAL OF CHROMATOGRAPHY | 1993年 / 629卷 / 02期
关键词
D O I
10.1016/0021-9673(93)87052-N
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Capillary electrophoresis (CE) and high-performance liquid chromatography (HPLC) are compared for the analytical separation of anthraquinone-1-sulphonate and its related impurities anthraquinone-2-sulphonate, anthraquinone-1,8-disulphonate and anthraquinone-1,5-disulphonate Optimum conditions for CE use a borate solution (50 mM NaH2BO3 and 8 mM H3BO3) as background electrolyte at pH 10.0, and for HPLC acetonitrile-water (60:40) containing 0.8% (w/v) cetyltrimethylammonium bromide as eluent. Analysis times are comparable by both techniques. Quantitative aspects including CE and HPLC efficiency, linearity, precision and limits of detection (LOD) arc compared. For anthraquinone-1-sulphonate the CE concentration LOD is 0.7 mug ml-1 and the HPLC LOD is 6 ng ml-1: mass LODs are 3 and 60 pg, respectively. Assay precision is 2% R.S.D. in peak area by CE using instruments from several manufacturers. This is improved to better than 0.5% R.S.D. in relative peak areas when a co-injected analyte is used as an internal standard, showing that injection is the factor limiting precision in CE. Integration errors give a significant contribution to the observed error in relative peak areas.
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收藏
页码:379 / 384
页数:6
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