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E. G. Lobanova

Publications and source records attributed to E. G. Lobanova.

2 recordsLinked to original sources

Efficient quantitative hyperspectral image unmixing method for large-scale Raman micro-spectroscopy data analysis

Vibrational micro-spectroscopy is a powerful optical tool, providing a non-invasive label-free chemically specific imaging for many chemical and biomedical applications. However, hyperspectral image produced by Raman micro-spectroscopy typically consists of thousands discrete pixel points, each having individual Raman spectrum at thousand wavenumbers, and therefore requires appropriate image unmixing computational methods to retrieve non-negative spatial concentration and corresponding non-negative spectra of the image biochemical constituents. In this article, we present a new efficient Quantitative Hyperspectral Image Unmixing (Q-HIU) method for large-scale Raman micro-spectroscopy data analysis. This method enables to simultaneously analyse multi-set Raman hyperspectral images in three steps: (i) Singular Value Decomposition with innovative Automatic Divisive Correlation (SVD-ADC) which autonomously filters spatially and spectrally uncorrelated noise from data; (ii) a robust subtraction of fluorescent background from the data using a newly developed algorithm called Bottom Gaussian Fitting (BGF); (iii) an efficient Quantitative Unsupervised/Partially Supervised Non-negative Matrix Factorization method (Q-US/PS-NMF), which rigorously retrieves non-negative spatial concentration maps and spectral profiles of the samples' biochemical constituents with no a priori information and with great operation speed. Alternatively, the Q-US/PS-NMF is capable to work as a partially supervised method, when one or several samples' constituents are known, which significantly widens chemical and biomedical applications of the method. We apply the Q-HIU to the analysis of real large-scale Raman hyperspectral images of human atherosclerotic aortic tissues and our results show a proof-of-principle for the proposed method to retrieve the biochemical composition of the tissues.

physics.comp-ph

Quantitative chemical imaging of amyloid-β plaques with Raman micro-spectroscopy in human Alzheimer's diseased brains

Alzheimer's disease (AD) is a neurodegenerative disorder and the most common cause of dementia in the elderly. The extracellular accumulation of amyloid-$β$ (A$β$) in senile plaques is a principal event in the pathogenesis and there is growing evidence that the dysregulation of lipid pathways is implicated in the disease, however the link between these two is still under study. In this work, we investigated human brain samples, from 11 AD patients and a control cohort of age-matched subjects without AD, using label-free chemically-specific Raman micro-spectroscopy. The collected image data were quantitatively analysed using an efficient quantitative unsupervised/partially supervised non-negative matrix factorization method, to retrieve the concentration maps and spectra of the samples' chemical constituents. Significant changes in lipid composition as well as increased concentrations of oxidative stress bio-markers were observed in AD tissues compared to the control. In particular, the analysis revealed accumulations of cholesteryl esters with saturated long-chain fatty acids (FAs), A$β$ fibrils, arachidic acid, fibrin, collagen-like amyloidogenic component (CLAC), $β$-carotene and magnetite, co-localising in A$β$ plaques of AD human brains and exhibiting concentrations highest at the fibrillar core and lowest at the rim. This finding opens perspectives for new anti-inflammatory and antioxidant drug strategies, designed to restore brain homeostasis as potential therapeutics of AD. We also demonstrate by the means of spatial concentration histograms that these identified species separate AD from non-demented control brains, beneficial for AD diagnosis.

physics.med-ph