化学成像——一个图像总是值一千个光谱吗?

Alessandra Sussulini
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Depending on the selected ionization technique, molecular or elemental images can be acquired. For molecular MSI, the classical matrix-assisted laser desorption/ionization (MALDI) is generally applied for imaging lipids, peptides and proteins, and the ambient ionization technique desorption electrospray ionization (DESI) is commonly applied for visualizing lipid distribution. In terms of elemental MSI, laser ablation inductively coupled plasma (LA-ICP) is undoubtedly the technique of choice, although nano-secondary ion mass spectrometry (nanoSIMS) can also be applied. Considering optical spectroscopy, the main techniques used nowadays are Raman and near-infrared radiation – NIR – spectroscopy for molecular imaging, and Synchrotron radiation X-ray fluorescence – SRXRF – and laser-induced breakdown spectroscopy – LIBS – for elemental imaging. Amongst these techniques, the best spatial resolutions are generally achieved by SRXRF (elemental imaging) and Raman spectroscopy (molecular imaging). Analytical chemistry advances in chemical imaging allow the acquisition of images with high spatial resolution, which is particularly interesting when studying specific regions or cell structures in a biological sample. For instance, in a Parkinson’s disease model, LA-ICP-MS images with good spatial resolution make the distinction of specific mouse brain regions possible and, consequently, the association of metal ion concentrations to each region,1 which is a relevant result considering micro-local metal speciation in neurodegenerative diseases. 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引用次数: 0

摘要

化学图像可以被描述为分布图,其将元素或分子的化学信息(例如质荷比(m/z)或波长)与其在给定样品中的强度和/或浓度相关联。这些图像通常通过质谱(MS)或光谱技术获得,其中最初采集数百或数千个光谱,并使用专用图像处理软件构建和编辑最终图片,以及选择和注释样本中的感兴趣区域、执行校准程序等。质谱成像(最好缩写为MSI,以区别于离子迁移率光谱法-IMS)是目前最常用的化学成像策略,正如最近发表的论文中所注意到的那样。根据所选择的电离技术,可以获得分子或元素图像。对于分子MSI,经典的基质辅助激光解吸/电离(MALDI)通常用于脂质、肽和蛋白质的成像,环境电离技术解吸电喷雾电离(DESI)通常用于可视化脂质分布。就元素MSI而言,激光烧蚀电感耦合等离子体(LA-ICP)无疑是首选技术,尽管纳米二次离子质谱(nanoSIMS)也可以应用。考虑到光谱,目前使用的主要技术是用于分子成像的拉曼和近红外辐射-NIR光谱,以及用于元素成像的同步辐射X射线荧光-SRXRF和激光诱导击穿光谱-LBS。在这些技术中,最佳的空间分辨率通常通过SRXRF(元素成像)和拉曼光谱(分子成像)来实现。化学成像中的分析化学进步允许获得具有高空间分辨率的图像,这在研究生物样品中的特定区域或细胞结构时特别有趣。例如,在帕金森病模型中,具有良好空间分辨率的LA-ICP-MS图像使特定小鼠大脑区域的区分成为可能,从而使金属离子浓度与每个区域的关联成为可能,1这是考虑到神经退行性疾病中微观局部金属物种形成的相关结果。然而,化学成像也存在一些缺陷,需要进一步的分析开发,例如分析时间长,缺乏用于定量分析和方法验证的认证参考材料,以及具有先进多元统计分析工具的开源软件。另一个需要克服的障碍涉及元素和分子成像结果的整合。自2009年以来,Becker和Jakubowski提出了关于以协同方式结合这些成像方法的第一篇综述文章,2直到最近在20203年和2021年的综述中进行了描述。这主要是因为每种成像技术都提供了不同的空间分辨率,使得图像叠加变得困难,而且还缺乏允许集成不同数据集以获得可靠结果并产生相关研究假设的软件和算法。除此之外,化学成像仪器的成本相当高,通常研究小组专门从事分子或元素成像。考虑到这些因素,重要的是要强调,参与化学成像研究的社区不仅应该关注生成的图像在分辨率方面的质量,而且,如果它们确实值得一千个光谱,还应该以深入和全面的方式解释最初的问题。毕竟,化学成像的主要目标是,图像代表了所研究的过程(疾病、治疗、污染、基因改造等)如何局部影响所研究的系统(生物、环境、药物样本),然后为解决不同领域的问题提供解决方案,如法医学、环境和生命科学。
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Chemical Imaging – Is an Image Always Worth a Thousand Spectra?
Chemical images can be described as distribution maps that correlate the chemical information of an element or molecule, such as mass-to-charge ratio (m/z) or wavelength, with its intensity and/or concentration in a given sample. These images are usually obtained by mass spectrometry (MS) or optical spectroscopy techniques, where hundreds or thousands of spectra are initially acquired and dedicated image processing software is employed to construct and edit the final pictures, as well as selecting and annotating regions of interest in a sample, performing calibration procedures, etc. Mass spectrometry imaging (preferably abbreviated as MSI, to distinguish it from ion mobility spectrometry – IMS) is currently the most employed chemical imaging strategy, as can be noticed in the most recently published papers. Depending on the selected ionization technique, molecular or elemental images can be acquired. For molecular MSI, the classical matrix-assisted laser desorption/ionization (MALDI) is generally applied for imaging lipids, peptides and proteins, and the ambient ionization technique desorption electrospray ionization (DESI) is commonly applied for visualizing lipid distribution. In terms of elemental MSI, laser ablation inductively coupled plasma (LA-ICP) is undoubtedly the technique of choice, although nano-secondary ion mass spectrometry (nanoSIMS) can also be applied. Considering optical spectroscopy, the main techniques used nowadays are Raman and near-infrared radiation – NIR – spectroscopy for molecular imaging, and Synchrotron radiation X-ray fluorescence – SRXRF – and laser-induced breakdown spectroscopy – LIBS – for elemental imaging. Amongst these techniques, the best spatial resolutions are generally achieved by SRXRF (elemental imaging) and Raman spectroscopy (molecular imaging). Analytical chemistry advances in chemical imaging allow the acquisition of images with high spatial resolution, which is particularly interesting when studying specific regions or cell structures in a biological sample. For instance, in a Parkinson’s disease model, LA-ICP-MS images with good spatial resolution make the distinction of specific mouse brain regions possible and, consequently, the association of metal ion concentrations to each region,1 which is a relevant result considering micro-local metal speciation in neurodegenerative diseases. Nevertheless, there are some drawbacks in chemical imaging that demand further analytical development, such as the long analysis time and the lack of certified reference materials for quantitative analysis and method validation, as well as open-source software with advanced multivariate statistical analysis tools. Another obstacle to overcome concerns the integration of elemental and molecular imaging results. Since 2009, when one of the first review articles regarding the combination of these imaging approaches in a synergistic way was proposed by Becker and Jakubowski,2 until more recently described in reviews from 20203 and 2021,4 it has been possible to realize that there is still much work to be done in this field. This is mostly due to the fact that each imaging technique provides different spatial resolutions, making image superposition difficult, and also the absence of software and algorithms that allow the integration of different data sets in order to obtain trustworthy results and produce relevant study hypotheses. Besides that, the instrumentation for chemical imaging is rather costly and usually research groups are specialized in either molecular or elemental imaging. With these considerations, it is important to emphasize that the community involved in chemical imaging research should focus not only on the quality of the generated images in terms of resolution but also, if they are indeed worth a thousand spectra, on interpretation of the initial questions in a deep and holistic manner. After all, the main objective of chemical imaging is that the images represent how the process in question (disease, treatment, contamination, genetic modification, etc.) locally affects the system (biological, environmental, pharmaceutical sample) under study and, then, provide solutions for solving problems in different areas, such as forensic, environmental and life sciences.
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