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用于痕量分析的在线半制备液相色谱-固相萃取-核磁共振系统的设计

The design of an on-line semi-preparative LC-SPE-NMR system for trace analysis.

作者信息

Xu Feng, Alexander Anthony J

机构信息

Analytical Research and Development, Bristol-Myers Squibb Pharmaceutical Research Institute, Wallingford, Connecticut 06492, USA.

出版信息

Magn Reson Chem. 2005 Sep;43(9):776-82. doi: 10.1002/mrc.1617.

Abstract

This paper reports the design of an on-line semi-preparative LC-SPE-NMR system and its use in the structural analysis of mixture components at the 0.02-1% level. The combination provides at least a five fold mass sensitivity increase over that obtained from typical analytical LC-SPE systems and a >30-fold total NMR sensitivity enhancement over analysis by LC-NMR. This is accomplished by using a novel on-line device to store, dilute (1-100-fold) and deliver (at an optimized flow-rate) the isolated component of interest to an SPE trap unit. The SPE unit consists of two cartridges connected in parallel to increase the overall SPE capacity and also to decrease the flow-rate through each trap for enhanced trapping efficiency. As the coupling of semi-preparative LC with NMR (through SPE) is well matched in terms of optimal mass loading for both techniques, only one LC-SPE cycle is required to enrich a 50 microg ml(-1) component (1% in a 5 mg ml(-1) mixture) for the acquisition of heteronuclear (1)H-(13)C NMR data using a conventional NMR flow probe. Furthermore, analytes at the 0.02% level (approximately 1 microg ml(-1)) can be studied using 2D (1)H NMR techniques if peak cuts from replicate sample injections (> or =3) are accumulated into the storage/dilution unit and the resulting solution processed by just one SPE trap and elute cycle.

摘要

本文报道了一种在线半制备液相色谱-固相萃取-核磁共振(LC-SPE-NMR)系统的设计及其在0.02%-1%水平混合物组分结构分析中的应用。该组合提供的质量灵敏度比典型的分析型LC-SPE系统至少提高了五倍,总NMR灵敏度比LC-NMR分析提高了30倍以上。这是通过使用一种新型在线装置来存储、稀释(1-100倍)并以优化流速将感兴趣的分离组分输送到SPE捕集单元来实现的。SPE单元由两个并联的柱管组成,以增加整体SPE容量,并降低通过每个捕集器的流速,从而提高捕集效率。由于半制备液相色谱与核磁共振(通过固相萃取)的耦合在两种技术的最佳质量负载方面匹配良好,因此只需一个LC-SPE循环就可以富集50μg/ml(5mg/ml混合物中的1%)的组分,以便使用传统的NMR流动探头采集异核1H-13C NMR数据。此外,如果将重复进样(≥3次)的峰切割物积累到存储/稀释单元中,并通过仅一个SPE捕集和洗脱循环处理所得溶液,则可以使用二维1H NMR技术研究0.02%水平(约1μg/ml)的分析物。

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