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Quantitative Online Liquid Chromatography-Surface-Enhanced Raman Scattering of Purine Bases

机译:嘌呤碱在线定量液相色谱-表面增强拉曼散射

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Raman spectroscopy has been of interest as a detection method for liquid chromatographic separations for a significant period of time, due to the structural information it can provide, allowing the identification and distinction of coeluting analytes. Combined with the rapidly advancing field of enhanced Raman techniques, such as surface-enhanced Raman scattering (SERS), the previous low sensitivity of Raman measurements has also been alleviated. At-line LC-SERS analyses, where SERS measurements are taken of fractions collected during or after HPLC separation have been shown to be sensitive and applicable to a wide variety of analytes; however, quantitative, real-time, online LC-SERS analysis at comparable sensitivity to existing methods, applicable to high-throughput experiments, has not been previously demonstrated. Here we show that by introducing silver colloid, followed by an aggregating agent into the postcolumn flow of an HPLC system, we can quantitatively and reproducibly analyze mixtures of purine bases, with limits of detection in the region of 100-500 pmol. The analysis is performed without the use of a flow cell, thereby eliminating previously detrimental memory effects.
机译:由于拉曼光谱可以提供结构信息,因此可以在很长一段时间内作为液相色谱分离的检测方法而引起人们的关注,因为它可以识别和区分共洗脱的分析物。结合增强拉曼技术(如表面增强拉曼散射(SERS))的快速发展领域,拉曼测量的先前低灵敏度也得到了缓解。在线LC-SERS分析表明,对HPLC分离期间或分离后收集的馏分进行SERS测量非常灵敏,适用于多种分析物;但是,以前尚未证明与适用于高通量实验的现有方法具有相当灵敏度的定量,实时,在线LC-SERS分析。在这里,我们表明,通过将胶体银和随后的聚集剂引入HPLC系统的柱后流中,我们可以定量和可重复地分析嘌呤碱的混合物,检测限在100-500 pmol范围内。在不使用流通池的情况下进行分析,从而消除了以前有害的记忆效应。

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