Manchester Interdisciplinary Biocentre, School of Chemical Engineering and Analytical Science, University of Manchester, Manchester M60 1QD, UK.
Mass Spectrom Rev. 2011 Jan-Feb;30(1):142-74. doi: 10.1002/mas.20275.
In principle mass spectral imaging has enormous potential for discovery applications in biology. The chemical specificity of mass spectrometry combined with spatial analysis capabilities of liquid metal cluster beams and the high yields of polyatomic ion beams should present unprecedented ability to spatially locate molecular chemistry in the 100 nm range. However, although metal cluster ion beams have greatly increased yields in the m/z range up to 1000, they still have to be operated under the static limit and even in most favorable cases maximum yields for molecular species from 1 µm pixels are frequently below 20 counts. However, some very impressive molecular imaging analysis has been accomplished under these conditions. Nevertheless although molecular ions of lipids have been detected and correlation with biology is obtained, signal levels are such that lateral resolution must be sacrificed to provide a sufficient signal to image. To obtain useful spatial resolution detection below 1 µm is almost impossible. Too few ions are generated! The review shows that the application of polyatomic primary ions with their low damage cross-sections offers hope of a new approach to molecular SIMS imaging by accessing voxels rather than pixels to thereby increase the dynamic signal range in 2D imaging and to extend the analysis to depth profiling and 3D imaging. Recent data on cells and tissue analysis suggest that there is, in consequence, the prospect that a wider chemistry might be accessible within a sub-micron area and as a function of depth. However, these advances are compromised by the pulsed nature of current ToF-SIMS instruments. The duty cycle is very low and results in excessive analysis times, and maximum mass resolution is incompatible with maximum spatial resolution. New instrumental directions are described that enable a dc primary beam to be used that promises to be able to take full advantage of all the capabilities of the polyatomic ion beam. Some new data are presented that suggest that the aspirations for these new instruments will be realized. However, although prospects are good, the review highlights the continuing challenges presented by the low ionization efficiency and the complications that arise from matrix effects.
原则上,质谱成像在生物学的发现应用中具有巨大的潜力。质谱的化学特异性与液态金属团簇束的空间分析能力相结合,以及多原子离子束的高产率,应该为在 100nm 范围内定位分子化学物质提供前所未有的能力。然而,尽管金属团簇离子束在 m/z 范围内高达 1000 的产率有了很大提高,但它们仍需在静态极限下运行,即使在最有利的情况下,来自 1μm 像素的分子物种的最大产率也经常低于 20 个计数。然而,在这些条件下已经完成了一些非常令人印象深刻的分子成像分析。尽管已经检测到脂质的分子离子,并与生物学相关联,但信号水平如此之低,以至于为了成像必须牺牲横向分辨率来提供足够的信号。要获得有用的空间分辨率,检测低于 1μm 的几乎是不可能的。产生的离子太少了!综述表明,具有低损伤截面的多原子初级离子的应用有望为分子 SIMS 成像提供一种新方法,通过访问体素而不是像素来增加 2D 成像中的动态信号范围,并将分析扩展到深度剖析和 3D 成像。最近关于细胞和组织分析的数据表明,因此,有可能在亚微米区域内并作为深度的函数访问更广泛的化学物质。然而,这些进展受到当前 ToF-SIMS 仪器的脉冲性质的限制。占空比非常低,导致分析时间过长,最大质量分辨率与最大空间分辨率不兼容。描述了新的仪器方向,使直流初级束能够被使用,这有望充分利用多原子离子束的所有能力。提出了一些新的数据,表明这些新仪器的期望将得到实现。然而,尽管前景很好,但综述强调了低电离效率和基质效应引起的复杂性带来的持续挑战。