首页> 外文期刊>Journal of Chromatography, Biomedical Applications >Discontinuous electrophoretic stacking system for cholate-based electrokinetic chromatographic separation of 8-hydroxy-2'-deoxygeuanosine from unmodified deoxynucleosides
【24h】

Discontinuous electrophoretic stacking system for cholate-based electrokinetic chromatographic separation of 8-hydroxy-2'-deoxygeuanosine from unmodified deoxynucleosides

机译:间断电泳堆叠系统,用于从未修饰的脱氧核苷中分离出基于胆酸盐的电动色谱,分离出8-羟基-2'-脱氧地质鹅苷

获取原文
获取原文并翻译 | 示例
       

摘要

The stacking and baseline-resolved separation of the oxidative damage marker, 8-hydroxy-2'-deoxyguanosine (8-OHdG), from unmodified deoxynucleosides in under 4 min is reported. Separations of 8-OHdG from 2'-deoxyadenosine, 2'-deoxycytosine, 2'-deoxyguanosine, and thymidine are accomplised using micellar electrokietic capillary chromatography with sodium cholate. Importantly, the use of sulfate, intentionally added to the sample matrix, results in effective stacking of 8-OHdG and other analytes. This work extends electrokinetic stacking injection of neutral analytes to include deoxynucleosides.- The procedure works well with either electrokinetic or hydrodynamic injection. The separation buffer and sample matrix composition were optimized to effect stacking conditions with an uncoated 50 #mu#m fused-silica capillary. The lower limit of detection for the analytes is in the nanomolar range, and is more than an order of magnitude lower than without stacking. With 30 s (5.7 cm) electrokinetic injections, stacking and baseline separation of 8-hydroxy-2'-deoxyguanosine from the unmodified nucleosides is accomplished, even in the presence of a 400-fold excess of unmodified deoxynucleosides.
机译:据报道,在不到4分钟的时间内,氧化损伤标记物8-羟基-2'-脱氧鸟苷(8-OHdG)与未修饰的脱氧核苷的堆积和基线分辨分离。使用胶束电动毛细管色谱和胆酸钠,将8-OHdG从2'-脱氧腺苷,2'-脱氧胞嘧啶,2'-脱氧鸟苷和胸苷中分离出来。重要的是,有意添加到样品基质中的硫酸盐的使用可有效堆积8-OHdG和其他分析物。这项工作扩大了中性分析物的电动叠加注射的范围,使其包括脱氧核苷。-该方法适用于电动或流体动力注射。优化分离缓冲液和样品基质的组成,以使用未涂覆的50#μ#m熔融石英毛细管影响堆积条件。分析物的检测下限在纳摩尔范围内,比没有堆积的检测下限低一个数量级。通过30 s(5.7 cm)电动进样,即使存在400倍过量的未修饰脱氧核苷,也可以完成8-羟基-2'-脱氧鸟苷与未修饰核苷的堆积和基线分离。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号