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Capillary electrophoresis of heparin and other glycosaminoglycans using a polyamine running electrolyte

机译:使用多胺运行电解质对肝素和其他糖胺聚糖的毛细管电泳

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This study involves the use of polyamines as potential resolving agents for the capillary electrophoresis (CE) of glycosaminoglycans (GAGs), specifically heparin, dermatan sulfate, chondroitin sulfate, over-sulfated chondroitin sulfate (OSCS), and hyaluronan. All of the compounds can be separated from each other with the exception of chondroitin sulfate and hyaluronan. Using optimization software, the final run conditions are found to be 200 mM ethylenediamine and 45.5 mM phosphate as the electrolyte with -14 V applied across a 50 μm ID x 24.5 cm fused silica capillary at 15 °C. The ion migration order, with OSCS as the last instead of the first peak, is in contrast to previous reports using either a high molarity TRIS or lithium phosphate run buffer with narrower bore capillaries. Total analysis time is 12.5 min and the relative standard deviation of the heparin migration time is about 2.5% (n=5). The interaction mechanism between selected polyamines and heparin is explored using conductivity measurements in addition to CE experiments to show that an ion-pairing mechanism is likely.
机译:这项研究涉及使用多胺作为糖胺聚糖(GAG)的毛细管电泳(CE)的潜在拆分剂,特别是肝素,硫酸皮肤素,硫酸软骨素,过度硫酸化软骨素(OSCS)和透明质酸。除硫酸软骨素和透明质酸外,所有化合物均可彼此分离。使用优化软件,最终运行条件为200 mM乙二胺和45.5 mM磷酸盐作为电解质,在15°C下跨50μmID x 24.5 cm熔融石英毛细管施加了-14 V电压。与OSCS作为最后一个峰而不是第一个峰的离子迁移顺序,与以前使用高摩尔浓度TRIS或磷酸锂运行缓冲液且毛细管孔径较窄的报道相反。总分析时间为12.5分钟,肝素迁移时间的相对标准偏差约为2.5%(n = 5)。除了进行CE实验外,还使用电导率测量法探索了选定的多胺与肝素之间的相互作用机理,以证明可能存在离子对机理。

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