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现代生物分析方法的最新趋势和进展综述:色谱法和样品制备。

A review of current trends and advances in modern bio-analytical methods: chromatography and sample preparation.

机构信息

Department of Analytical Chemistry, Faculty of Pharmacy, Charles University, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.

出版信息

Anal Chim Acta. 2009 Dec 10;656(1-2):8-35. doi: 10.1016/j.aca.2009.10.004. Epub 2009 Oct 8.

DOI:10.1016/j.aca.2009.10.004
PMID:19932811
Abstract

Any bio-analytical method includes several steps, all of them being important in order to achieve reliable results. The first step is taking aliquots of samples for the analysis, followed by the extraction procedure and sample clean-up, chromatographic analysis and detection. Chromatographic methods, particularly liquid chromatography, are the methods of choice in bio-analytical laboratories. Current trends in fast liquid chromatographic separations involve monolith technology, fused core columns, high temperature liquid chromatography and ultra-high performance liquid chromatography (UHPLC). UHPLC has recently become a wide-spread analytical technique in many laboratories which focus on fast and sensitive bio-analytical assays. The key advantages of UHPLC are the increased speed of analysis, higher separation efficiency and resolution, higher sensitivity and much lower solvent consumption as compared to other analytical approaches. This is all enabled by specially designed instruments and sub-2-microne particle packed analytical columns. There is a great contrast between ultra-fast chromatographic analysis and conventional sample preparation, which remains highly labor-intensive and time-consuming. Conventional sample preparation techniques including SPE, solid phase extraction; LLE, liquid-liquid extraction; PP, protein precipitation and many modern approaches (RAM, restricted access material; MIP, molecularly imprinted polymers; SPME, solid phase microextraction; LLME, liquid-liquid microextraction; MEPS, microextraction by packed sorbent and many others) have also been featured as fundamental and critical step of bio-analytical methods.

摘要

任何生物分析方法都包括几个步骤,所有步骤对于获得可靠的结果都很重要。第一步是取样品进行分析的等分试样,接着是提取程序和样品净化、色谱分析和检测。色谱方法,特别是液相色谱法,是生物分析实验室的首选方法。目前快速液相色谱分离的趋势涉及整体柱技术、熔融核柱、高温液相色谱和超高效液相色谱(UHPLC)。UHPLC 最近已成为许多专注于快速和灵敏生物分析测定的实验室中的广泛应用的分析技术。UHPLC 的主要优点是分析速度加快、分离效率和分辨率提高、灵敏度提高,与其他分析方法相比,溶剂消耗大大降低。这一切都是通过专门设计的仪器和亚 2 微米颗粒填充的分析柱实现的。超快速色谱分析与传统的样品制备之间存在着巨大的差异,后者仍然高度劳动密集和耗时。传统的样品制备技术包括 SPE(固相萃取)、LLE(液液萃取)、PP(蛋白质沉淀)和许多现代方法(RAM(限制存取材料)、MIP(分子印迹聚合物)、SPME(固相微萃取)、LLME(液液微萃取)、MEPS(填充吸附剂微萃取)等)也被作为生物分析方法的基本和关键步骤。

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