Determination of the diol content of chromatographic supports by capillary electrophoresis

被引:29
作者
Chattopadhyay, A [1 ]
Hage, DS [1 ]
机构
[1] UNIV NEBRASKA,DEPT CHEM,LINCOLN,NE 68588
关键词
stationary phases; LC; diols;
D O I
10.1016/S0021-9673(96)00742-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A capillary electrophoresis (CE) method was developed for determining the diol content of supports used in high-performance affinity or size exclusion chromatography. This method involved oxidizing the diol-bonded support with periodate, followed by the use of CE to separate and quantitate the iodate produced by this reaction. Both the oxidation and separation conditions were considered in optimizing this assay. The final method was performed by reacting a known amount of support with a 20-fold excess of periodate in pH 4.0, 0.5 M acetate buffer, with pyromellitic acid being used as an internal standard. After allowing 5-10 min for oxidation, the mixture was filtered and the filtrate was injected onto a 57 cmx50 mu m I.D. fused-silica capillary operated at 25 kV and containing pH 4.0, 0.5 M acetate as the running buffer. The total separation time was 5 min per run and gave a detection limit of 0.1 mM iodate (or 0.1 mu mol diol groups) for a 6-nl injection of a 1-ml reaction mixture. By varying the amount the support that was assayed, this method could be used with either porous or non-porous supports. This technique showed good correlation with an iodometric titration but required much less sample and time to perform.
引用
收藏
页码:255 / 261
页数:7
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