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Analysis of glycosaminoglycan-derived disaccharides by capillary electrophoresis using laser-induced fluorescence detection

机译:用激光诱导荧光检测分析毛细管电泳的糖胺聚糖衍生的二糖

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摘要

A quantitative and highly sensitive method for the analysis of glycosaminoglycan (GAG)-derived disaccharides is presented that relies on capillary electrophoresis (CE) with laser-induced fluorescence (LIF) detection. This method enables complete separation of seventeen GAG-derived disaccharides in a single run. Unsaturated disaccharides were derivatized with 2-aminoacridone (AMAC) to improve sensitivity. The limit of detection was at the attomole level and about 100-fold more sensitive than traditional CE-ultraviolet detection. A CE separation timetable was developed to achieve complete resolution and shorten analysis time. The RSD of migration time and peak areas at both low and high concentrations of unsaturated disaccharides are all less than 2.7% and 3.2%, respectively, demonstrating that this is a reproducible method. This analysis was successfully applied to cultured Chinese hamster ovary cell samples for determination of GAG disaccharides. The current method simplifies GAG extraction steps, and reduces inaccuracy in calculating ratios of heparin/heparan sulfate to chondroitin sulfate/dermatan sulfate, resulting from the separate analyses of a single sample.
机译:提出了用于分析糖胺聚糖(GAG)的多糖的定量和高敏感方法,其依赖于激光诱导的荧光(LiF)检测毛细管电泳(CE)。该方法能够在单次运行中完全分离17个GAG衍生的二糖。用2-氨基吖啶酮(AMAC)衍生不饱和二糖以提高敏感性。检测极限在抗替摩水平和比传统的CE-紫外检测比传统的CE-紫外检测更敏感的约100倍。开发了CE分离时间表,以实现完整的分辨率和缩短分析时间。迁移时间和低浓度的不饱和二糖的峰值区域的RSD分别小于2.7%和3.2%,证明这是一种可重复的方法。该分析已成功应用于培养的中国仓鼠卵巢细胞样品,用于测定堵嘴二糖。目前的方法简化了GAG提取步骤,并降低了计算肝素/硫酸乙肝素硫酸盐/皮肤硫酸盐硫酸盐/皮肤硫酸盐的比率的不准确性,由单个样品的单独分析产生。

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