Abstract:Mid-infrared spectroscopic imaging (MIRSI) is an emerging class of label-free techniques being leveraged for digital histopathology. Optical photothermal infrared (O-PTIR) is based on vibrational absorbance imaging using a pump-probe architecture capable of a 10x enhancement in spatial resolution relative to FTIR imaging. This allows truly sub-cellular spectroscopic investigation of tissue at biochemically important fingerprint wavelengths. Modern histopathologic identification of ovarian cancer involves tissue staining followed by morphological pattern recognition. This process is time-consuming, subjective, and requires extensive expertise. In this paper, we present the first label-free automated histological classification of ovarian tissue sub-types using MIRSI. We demonstrate that enhanced resolution of sub-cellular features, combined with spectroscopic information, enables reliable classification (0.98 AUC) of ovarian cell sub-types. Moreover, we present statistically robust validation from 74 patient samples with over 60 million data points. This demonstrates that sub-cellular resolution from five wavenumbers is sufficient to outperform state-of-the-art diffraction-limited techniques from up to 374 different wavenumbers. O-PTIR also performs measurements in back-reflection geometry, opening the door to future in vivo studies on glass slides.
Abstract:Spectral imaging enables spatially-resolved identification of materials in remote sensing, biomedicine, and astronomy. However, acquisition times require balancing spectral and spatial resolution with signal-to-noise. Hyperspectral imaging provides superior material specificity, while multispectral images are faster to collect at greater fidelity. We propose an approach for fusing hyperspectral and multispectral images to provide high-quality hyperspectral output. The proposed optimization leverages the least absolute shrinkage and selection operator (LASSO) to perform variable selection and regularization. Computational time is reduced by applying the alternating direction method of multipliers (ADMM), as well as initializing the fusion image by estimating it using maximum a posteriori (MAP) based on Hardie's method. We demonstrate that the proposed sparse fusion and reconstruction provides quantitatively superior results when compared to existing methods on publicly available images. Finally, we show how the proposed method can be practically applied in biomedical infrared spectroscopic microscopy.