毛细管电泳法分析藏红花植物细胞多糖中单糖组成  

Analysis of monosaccharides in the saffron corm glycoconjugate by capillary electrophoresis

作　　者：马海宁[1] 华玉娟[1] 屠春燕[1] 袁丽红[1] 韦萍[1] 

机构地区：[1]南京工业大学生物与制药工程学院,江苏南京210009

出　　处：《色谱》2012年第3期304-308,共5页Chinese Journal of Chromatography

基　　金：国家重点基础研究发展计划项目(2009CB724700)

摘　　要：以对甲氧基苯胺为衍生试剂,采用毛细管电泳法分析了藏红花植物细胞多糖中的单糖组成。对衍生条件进行了优化,并对毛细管分离条件进行了系统的研究。衍生反应在醋酸含量9.5%(v/v)、80℃下反应2 h的衍生产率最大,衍生产物紫外检测波长234 nm。在优化的毛细管电泳分离条件(未涂层熔融石英毛细管柱(60 cm(有效长度50 cm)×50μm),柱温25℃,电压20 kV,使用350 mmol/L硼酸电解液(pH 10.21),压力(3.447 5 kPa)进样5s)下,基线分离了11种结构相近的醛糖(来苏糖、木糖、核糖、葡萄糖、甘露糖、半乳糖、鼠李糖、纤维二糖、麦芽糖、乳糖)、酮糖(果糖)的衍生产物。应用该方法定量检测了藏红花植物细胞多糖水解物中糖的成分,各糖的回收率为94.3%～105.4%,相对标准偏差为3.3%～4.6%。The monosaccharides in the saffron corm glycoconjugate were separated by capillary electrophoresis （CE） coupled with pre-column derivatization. 4-Methoxyaniline was used as derivatization reagent. The derivatization and CE separation conditions were investigated. The ultraviolet detection wavelength was 234 nm. The maximum yield of this derivatization reactionwas obtained under the presence of 9.5% （v/v） acetic acid at 80 22 for 2 h. An uncoated fused-silica capillary of 50μm i. d. and 50/60 cm length （ effective length/total length） was employed, and a pressure injection （3. 447 5 kPa, 5 s） was applied. The baseline separation of l 1 monosaccharides and disaccharides （lyxose, xylose, ribose, glucose, mannose, galactose,rhamnose, cellobiose, maltose, lactose, fructose） was reached at 25 ℃, 20 kV of separation voltage and with 350 mmol/L boric acid （pH 10. 21 ） as running buffer. The developed method has been successfully applied to quantitatively determine the components of saffron corm glyco- conjugate, and the results showed that the recovery of each monosaccharide was in the range of 94.3% -105.4%, the relative standard deviation was 3.3% -4.5%.

关 键 词：毛细管电泳 对甲氧基苯胺 柱前衍生 单糖 酮糖 多糖 藏红花 

分 类 号：O658[理学—分析化学]