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大面积样本快速质量显微镜技术的改进。

Improvements in Fast Mass Microscopy for Large-Area Samples.

作者信息

Sandström Edith, Huysmans Pascal, Giskes Frans, Laeven Paul, Van Nuffel Sebastiaan, Heeren Ron M A, Anthony Ian G M

机构信息

The Maastricht MultiModal Molecular Imaging Institute (M4i), Division of Imaging Mass Spectrometry, Maastricht University, Maastricht 6229 ER, The Netherlands.

Instrument Development, Engineering & Evaluation (IDEE), Maastricht University, Maastricht 6229 ER, The Netherlands.

出版信息

Anal Chem. 2024 Nov 12;96(45):18037-18042. doi: 10.1021/acs.analchem.4c03480. Epub 2024 Oct 28.

DOI:10.1021/acs.analchem.4c03480
PMID:39467711
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11561871/
Abstract

Mass spectrometry imaging (MSI) is a technique that analyzes the chemical information and spatial distribution of surface analytes. Most MSI studies are conducted in microprobe mode, in which a mass spectrum is collected for each pixel to create a mass image. Thus, the spatial resolution, sample imaging area, and imaging speed are linked. In this mode, halving the pixel size quadruples the analytical time, which presents a practical limit on the high spatial resolution MSI throughput. Fast mass microscopy (FMM) is, in contrast, a microscope-mode MSI technique that decouples spatial resolution and imaging speed. FMM circumvents the linear-quadratic relationship of pixel size and analytical time, which enables increased imaging size area and the analytical speed achievable. In this study, we implement instrument modifications to the FMM system, including the addition of linear encoders that enable roughly 8.5× faster imaging than was previously achieved, allowing a 42.5 × 26 mm sample area to be imaged at a 1 μm pixel size in <4.5 min. Linear encoders also enable the alignment of multipass images that increase image homogeneity and signal intensity. The applicability of FMM to large area samples has made it important to define the tolerance to height variations of the technique, which was determined to be at least 218 ± 0.03 ( = 3) μm.

摘要

质谱成像(MSI)是一种分析表面分析物化学信息和空间分布的技术。大多数MSI研究是在微探针模式下进行的,即对每个像素收集质谱以创建质量图像。因此,空间分辨率、样品成像面积和成像速度是相互关联的。在这种模式下,将像素尺寸减半会使分析时间增加四倍,这对高空间分辨率MSI的通量构成了实际限制。相比之下,快速质量显微镜(FMM)是一种显微镜模式的MSI技术,它将空间分辨率和成像速度解耦。FMM规避了像素尺寸与分析时间的线性二次关系,从而能够增加成像面积并提高分析速度。在本研究中,我们对FMM系统进行了仪器改进,包括添加线性编码器,其使成像速度比以前提高了约8.5倍,能够在不到4.5分钟的时间内以1μm的像素尺寸对42.5×26mm的样品区域进行成像。线性编码器还能够对齐多通道图像,从而提高图像均匀性和信号强度。FMM对大面积样品的适用性使得定义该技术对高度变化的耐受性变得很重要,其被确定为至少218±0.03(=3)μm。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07bd/11561871/8401a4b6c953/ac4c03480_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07bd/11561871/f6e089c33858/ac4c03480_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07bd/11561871/bb5b2788fa14/ac4c03480_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07bd/11561871/8401a4b6c953/ac4c03480_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07bd/11561871/f6e089c33858/ac4c03480_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07bd/11561871/bb5b2788fa14/ac4c03480_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07bd/11561871/8401a4b6c953/ac4c03480_0003.jpg

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Development of High Throughput Microscope Mode Secondary Ion Mass Spectrometry Imaging.高通量显微镜模式二次离子质谱成像的发展。
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Talanta. 2023 Nov 1;264:124721. doi: 10.1016/j.talanta.2023.124721. Epub 2023 May 27.
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Time of acquisition and high spatial resolution mass spectrometry imaging.采集时间和高空间分辨率质谱成像。
J Mass Spectrom. 2023 Mar;58(3):e4911. doi: 10.1002/jms.4911.
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