激光解吸电离质谱法在天然产物研究中的新进展

A. Schinkovitz, D. Séraphin, P. Richomme
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摘要

质谱(MS)是天然产物(NPs)结构鉴定不可或缺的工具,是分析化学研究的主要热点之一。这项技术长期以来一直用于获得分子质量和进一步的分子式。在过去,以前的电离源,如电子冲击(EI)限制了质谱分析主要挥发性,极性和耐热性化合物。然而,电喷雾电离(ESI)、大气压化学电离(APCI)和激光解吸/电离(LDI)等软电离技术的发展,使质谱分析的范围逐渐扩展到更广泛的化学实体。此外,液相色谱和气相色谱与质谱(LC - MS, GC - MS)的结合为复杂混合物和NPs的分析提供了最强大的工具。事实上,LC - MS通常被认为是首选的方法,特别是在研究复杂的小分子混合物时。另一方面,基质辅助激光解吸/电离(MALDI)和LDI的最新发展可能为该方法提供有用的补充和潜在的替代方法。这两种方法的电离机制相似,但略有不同。MALDI使用包含强紫外发色团(基质)的小分子将激光能量转移到样品材料,而LDI的目标化合物可以在没有任何基质支持的情况下通过激光照射直接电离。此外,某些具有LDI性质的化合物也可以用作MALDI矩阵。对于NPs的研究,MALDI和LDI可能有助于克服LC - MS中遇到的某些限制,例如在分析生物碱时不可缺少的缓冲溶液。此外,由于(MA)LDI几乎不需要任何样品调理,因此可以显著缩短分析时间。考虑到这些,接下来的文章将重点介绍一些有趣的MALDI和LDI应用程序,它们的重点是检测复杂混合物中的np。这包括使用专门适应的基质来选择性检测生物碱(i),研究固有的LDI和酚类化合物的基质特性(ii),以及评估LDI信号模式的可重复性(iii)。最终,LDI分析的统计方法将被提出(iv),这可能为将来的大样品批次的质量控制提供工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Developments of Laser Desorption Ionization Mass Spectrometry in Natural Products Research
Mass spectrometry (MS) represents an indispensable tool for the structural identification of natural products (NPs) and is one of the major focus areas of analytical chemistry research. The technique has long been used to obtain molecular weights and further molecular formulae. In the past, former ionization sources such as electronic impact (EI) limited MS analysis to predominately volatile, polar, and thermostable compounds. However, the development of soft ionization techniques such as electrospray ionization (ESI), atmospheric pressure chemical ionization (APCI), and laser desorption/ionization (LDI) have gradually extended the scope of MS analysis to a much wider range of chemical entities. Moreover, the hyphenation of liquid and gas chromatography with MS (LC‐MS, GC‐MS) has provided a most powerful tool for the analysis of complex mixtures and NPs. In fact, LC‐MS is often considered as a method of first choice particularly when studying complex mixtures of small molecules. On the other hand, recent developments in matrix‐assisted laser desorption/ionization (MALDI) and LDI may provide useful supplements and potential alternatives to this approach. Both methods share similar, though slightly different ionization mechanisms. While MALDI uses small molecules comprising strong UV chromophores (matrices) to transfer laser energy to the sample material, LDI targets compounds that can be directly ionized by laser irradiation without any matrix support. Moreover, certain compounds showing LDI properties may also work as MALDI matrices. With regard to NPs research, MALDI and LDI may help overcoming certain limitations encountered in LC‐MS such as the indispensable use of buffer solutions when analyzing alkaloids. Moreover, as (MA)LDI hardly requires any sample conditioning, analysis time can be significantly shortened. With all this in mind, the subsequent article will highlight some interesting MALDI and LDI applications, which focus on the detection of NPs in complex mixtures. This includes the use of specifically adapted matrices for the selective detection of alkaloids (i), the study of the inherent LDI and matrix properties of phenolic compounds (ii) as well of evaluation on the reproducibility of LDI signal patterns (iii). Eventually, a statistical approach toward LDI profiling, which may provide a future tool for quality control of large sample batches will be presented (iv).
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