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FTIR-spectroscopic and LA-ICP-MS imaging for combined hyperspectral image analysis of tumor modelsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ay01369h
Modern chemical imaging techniques provide spatially resolved information on the molecular and elemental composition of samples with both high spatial and spectral resolution. Over the past few decades these techniques, in particular, Fourier transform infrared (FTIR) spectroscopy and laser ablation...
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Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | Modern chemical imaging techniques provide spatially resolved information on the molecular and elemental composition of samples with both high spatial and spectral resolution. Over the past few decades these techniques, in particular, Fourier transform infrared (FTIR) spectroscopy and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) have been successfully applied in histopathological research. This work demonstrates that the multivariate analysis of combined FTIR and LA-ICP-MS microscopy hyperspectral images can bring additional knowledge to biomedical research. The concept of such analysis was demonstrated while investigating two different tumor samples subjected to anticancer therapy. Combined analysis has revealed a correlation between the lateral distribution of analytes and sample properties within the different techniques. Correlations between alterations in the average protein secondary structure and platinum distribution were found, as well as between changes in the cell nuclear morphology and a reduction of physiologically relevant trace elements. The results of combined analysis suggested different degrees of tumor viability. Univariate analysis and
k
-means clustering successfully discriminated dead tumor regions and supported the results of combined analysis.
Advantages of combined image analysis were demonstrated using infrared spectroscopy and mass spectrometry while characterizing biochemical changes occurring in tumor models. |
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ISSN: | 1759-9660 1759-9679 |
DOI: | 10.1039/c7ay01369h |