显微镜
薄层荧光显微镜
光学
材料科学
激光器
拉曼光谱
光电子学
激光灯
扫描共焦电子显微镜
物理
作者
Israel Rocha‐Mendoza,Jacob Licea‐Rodriguez,Mónica Marro,Omar E. Olarte,Marcos Antonio Plata-Sanchez,Pablo Loza‐Álvarez
摘要
We perform rapid spontaneous Raman 2D imaging in light-sheet microscopy using continuous wave lasers and interferometric tunable filters.By angularly tuning the filter, the cut-on/off edge transitions are scanned along the excited Stokes wavelengths.This allows obtaining cumulative intensity profiles of the scanned vibrational bands, which are recorded on image stacks; resembling a spectral version of the knife-edge technique to measure intensity profiles.A further differentiation of the stack retrieves the Raman spectra at each pixel of the image which inherits the 3D resolution of the host light sheet system.We demonstrate this technique using solvent solutions and composites of polystyrene beads and lipid droplets immersed in agar and by imaging the C-H (2800-3100 cm -1 ) region in a C. elegans worm.The image acquisition time results in 4 orders of magnitude faster than confocal point scanning Raman systems, allowing the possibility of performing fast spontaneous Raman•3D-imaging on biological samples.
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