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Dual fluorescence and electrochemical detection on an electrophoresis microchip

机译:电泳微芯片上的双重荧光和电化学检测

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Simultaneous amperometitic and fluorescence detection in a microfabricated electrophoresis chip is reported. Detection limits of 448 nM and 1.52, 16, and 28 muM have been achieved for dopamine, catechol, NBD-arginine, and NBD-phenylalanine, respectively. These two orthogonal detection schemes allow analysis of a wider spectrum of compounds per separation, leading to higher throughput and enabling resolution of two neutral analytes, NBD-arginine and catechol. In addition, insight into the detection and separation mechanisms is realized. Differences in migration time and peak widths between the two detectors are compared, providing a better understanding of detector alignment. A common problem encountered in electrophoresis is run-to-run migration time irreproducibility for certain samples. This novel microchip dual detection system has been utilized to reduce this irreproducibility. An unknown sample is monitored with one detector while a standard (i.e., ladder) is added to the sample and monitored simultaneously with the other detector. This dual detection method is demonstrated to normalize unknown peak mobilities in a cerebral spinal fluid sample. [References: 46]
机译:报告了在微型电泳芯片中同时进行安培和荧光检测。多巴胺,邻苯二酚,NBD-精氨酸和NBD-苯丙氨酸的检出限分别为448 nM和1.52、16和28μM。这两种正交检测方案可对每次分离的化合物进行更广谱的分析,从而提高通量,并能够分离两种中性分析物NBD-精氨酸和邻苯二酚。另外,实现了对检测和分离机制的了解。比较了两个检测器之间迁移时间和峰宽的差异,从而更好地了解了检测器对准。电泳中遇到的一个常见问题是某些样品的逐批迁移时间不可再现。这种新颖的微芯片双重检测系统已被用来减少这种不可重复性。用一个检测器监测未知样品,同时将标准品(即阶梯)添加到样品中,并与另一检测器同时监测。事实证明,这种双重检测方法可以使脑脊髓液样本中的未知峰迁移率正常化。 [参考:46]

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