High spatial resolution imaging of melanoma tissue by femtosecond laser-induced breakdown spectroscopy

The classification and imaging of melanoma embedded in murine skin tissue by femtosecond laser-induced breakdown spectroscopy (fs-LIBS) is reported. The tissue samples were collected from hairless mice with induced melanoma, cryosectioned to 50 μm thickness, and analyzed with no other sample treatment. LIBS measurement was carried out using an ultraviolet (UV) fs-laser (λ = 343 nm, τ = 550 fs) and intensified charge coupled device detector. The support vector machine (SVM) classifier is customized to distinguish melanoma and dermis with dominant peaks and their intensity ratios, of which normal distribution are obtained by maximum likelihood estimation. Based on the classifiers, a classification accuracy of about 97.9% was achieved by using the SVM algorithm adopting 3rd order polynomial kernel. LIBS mapping was carried out at the spatial resolution of about 15 μm. The LIBS mapping image to which a posterior probabilistic interpretation of the SVM results was applied agreed closely to the hematoxylin and eosin (H&E) staining image. It was shown that LIBS imaging can identify the tissue area of cancer and also inflammatory cells. The results showed that UV-fs-LIBS could be a useful alternative or supporting tool for melanoma screening. [Display omitted] •High spatial resolution (15 μm) LIBS imaging of cutaneous melanoma using a UV fs-laser.•Direct analysis of the cryosectioned tissue with no pretreatment of sample.•Capable to identify latent tumor and inflammatory cells.