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衍生化单糖和寡糖的毛细管电色谱法

Capillary electrochromatography of derivatized mono- and oligosaccharides.

作者信息

Yang C, El Rassi Z

机构信息

Department of Chemistry, Oklahoma State University, Stillwater 74078-3071, USA.

出版信息

Electrophoresis. 1998 Sep;19(12):2061-7. doi: 10.1002/elps.1150191204.

Abstract

An octadecyl-silica (ODS) stationary phase with light surface coverage of octadecyl ligands was introduced for capillary electrochromatography (CEC) at moderate electroosmotic flow (EOF) velocity. The ODS stationary phase was intentionally produced with light surface coverage in order to ensure a moderate EOF velocity across the packed capillary column, thus allowing relatively rapid analysis time. Despite the fact that the stationary phase leaves 75% of the surface silanols unreacted, fused-silica capillary columns packed with this ODS stationary phase exhibited reversed-phase behavior toward neutral alkylbenzene homologous solutes using hydroorganic eluents. Closely related p-nitrophenylglycosides including some p-nitrophenyl-monosaccharides and p-nitrophenyl-maltooligosaccharides were readily separated on the ODS capillary column within a relatively short analysis time. Also, alpha- and beta-anomers of some p-nitrophenyl-monosaccharides were readily separated in the presence of a small amount of borate buffer in the hydroorganic eluent.

摘要

引入了一种十八烷基配体表面覆盖度较低的十八烷基硅胶(ODS)固定相,用于在中等电渗流(EOF)速度下的毛细管电色谱(CEC)。故意制备表面覆盖度较低的ODS固定相,以确保在填充毛细管柱中具有中等的EOF速度,从而实现相对较短的分析时间。尽管该固定相有75%的表面硅醇未反应,但填充这种ODS固定相的熔融石英毛细管柱在使用有机改性剂洗脱液时,对中性烷基苯同系物溶质表现出反相行为。包括一些对硝基苯基单糖和对硝基苯基麦芽低聚糖在内的密切相关的对硝基苯基糖苷,在相对较短的分析时间内很容易在ODS毛细管柱上分离。此外,在有机改性剂洗脱液中存在少量硼酸盐缓冲液的情况下,一些对硝基苯基单糖的α-和β-异构体很容易分离。

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