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The use of hydrazine based derivatisation reagents for improved sensitivity and detection of carbonyl containing compounds 'on tissue' using MALDI-MS

机译:使用肼基衍生化试剂改善了使用MALDI-MS的含含肼的含羰基化合物“组织”的敏感性和检测

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The microscope images in Figure 1 show the crystal formation of the 2,4-Dinitrophenylhydrazine reactive matrix observed under the current conditions described. These images show that under these conditions the crystals are not uniform or evenly distributed, as would be expected for those of more conventional MALDI matrices. Figure 2 shows the MALDI-MS images of the distribution of the radical cation ([M]~(+centre dot)) m/z 500, hydrazone derivative ([M_(D)+H]~(+)) m/z 681, sodium adduct ([M+Na]~(+)) m/z 523 and potassium adduct ([M+K]~(+)) m/z 539 of Fluticasone Propionate within the spiked areas of the lung tissue. These images show that the reactive matrix can be used to produce MALDI-MS imaging data. However, the lack of linearity of the response with respect to concentration spiked needs to be investigated further. The cause may be related to the compound spiking methods and / or matrix application.
机译:图1中的显微镜图像显示了在所描述的当前条件下观察到的2,4-二硝基苯基肼反应性基质的晶体形成。 这些图像显示,在这些条件下,晶体不均匀或均匀分布,所以预期的那些传统的MALDI矩阵的预期将是如此。 图2显示了自由基阳离子分布的MALDI-MS图像([M]〜(+中心点))M / Z 500,腙衍生物([M_(D)+ H]〜(+))m / z 681,钠加合物([M + Na]〜(+))M / Z 523和钾加合物([M + K]〜(+))M / Z 539在肺组织的尖刺区域内丙酸盐。 这些图像表明,反应矩阵可用于产生MALDI-MS成像数据。 然而,需要进一步调查关于浓度掺入的响应的线性度。 原因可能与复合尖峰方法和/或基质施用有关。

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