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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >High-sensitivity detection of biological amines using fast Hadamard transform CE coupled with photolytic optical gating.
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High-sensitivity detection of biological amines using fast Hadamard transform CE coupled with photolytic optical gating.

机译:使用快速Hadamard转换CE和光解光学选通的高灵敏度检测生物胺。

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摘要

Here, we report the first utilization of Hadamard transform CE (HTCE), a high-sensitivity, multiplexed CE technique, with photolytic optical gating sample injection of caged fluorescent labels for the detection of biologically important amines. Previous implementations of HTCE have relied upon photobleaching optical gating sample injection of fluorescent dyes. Photolysis of caged fluorescent labels reduces the fluorescence background, providing marked enhancements in sensitivity compared to photobleaching. Application of fast Hadamard transform CE (fHTCE) for fluorescein-based dyes yields a ten-fold higher sensitivity for photolytic injections compared to photobleaching injections, due primarily to the reduced fluorescent background provided by caged fluorescent dyes. Detection limits as low as 5 pM (ca. 18 molecules per injection event) were obtained with on-column LIF detection using fHTCE in less than 25 s, with the capacity for continuous, online separations. Detection limits for glutamate and aspartate below 150 pM (1-2 amol/injection event) were obtained using photolytic sample injection, with separation efficiencies exceeding 1 x 10(6) plates/m and total multiplexed separation times as low as 8 s. These results strongly support the feasibility of this approach for high-sensitivity dynamic chemical monitoring applications.
机译:在这里,我们报告了首次利用Hadamard转换CE(HTCE),一种高灵敏度的多路复用CE技术,通过光解光学门控样品注入笼状荧光标记物来检测重要的生物胺。 HTCE的先前实现方式依赖于荧光染料的光漂白光学门控样品注入。笼状荧光标记的光解作用减少了荧光背景,与光漂白相比,灵敏度显着提高。快速Hadamard变换CE(fHTCE)在荧光素基染料上的应用与光漂白注射剂相比,对光解注射剂的灵敏度提高了十倍,这主要是由于笼状荧光染料所提供的荧光背景降低了。使用fHTCE在少于25 s的时间内进行柱上LIF检测,可实现低至5 pM的检测限(每个进样事件大约18个分子),并具有连续在线分离的能力。使用光解样品进样获得的谷氨酸和天冬氨酸的检出限低于150 pM(1-2 amol /进样事件),分离效率超过1 x 10(6)板/ m,总多重分离时间低至8 s。这些结果强烈支持了这种方法在高灵敏度动态化学监测应用中的可行性。

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