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ABSTRACT: Purpose
Current skin imaging modalities, including optical, electron, and confocal microscopy, mostly require tissue fixations that could damage proteins and biological molecules. Live tissue or cell imaging such as ultrasonography and optical coherent microscope may not adequately measure the dynamic spectroscopical changes. Raman spectroscopy has been adopted for skin imaging in vivo, mostly for skin cancer imaging. However, whether the epidermal and dermal thickening in skin could be measured and distinguished by conventional Ramen spectroscopy or the surface-enhanced Raman scattering (SERS), a rapid and label-free method for noninvasive measurement remains unknown.Methods
Human skin sections from patients of atopic dermatitis and keloid, which represent epidermal and de
SUBMITTER: Huang PJ
PROVIDER: S-EPMC10316472 | biostudies-literature | 2023 May
REPOSITORIES: biostudies-literature