Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · 2010 · 11 citations · 0 references
Natural SciencesBiophysicsCell BiologyBiomedical ImagingCell BiophysicsHistologyCellular ImagingCellular UltrastructureFluorescence MicroscopyLabel-free ImagingMicroscopic Cell MorphologySpecimen PreparationBright-field ImagingBright-field MicroscopyDigital Holographic MicroscopyPhase-contrast ImagingPhase-contrast MicroscopyQuantitative Phase ImagingSubcellular ImagingSubcellular Ultrastructure
Digital holographic microscopy (DHM) provides label-free quantitative phase contrast with low demands on sample preparation. Nevertheless, for DHM measurements on fixed cells the mounting medium has to be considered while the phase contrast of living cells may be influenced by the used buffer solution. To quantify these effects, the maximum cell caused phase contrast and the visibility of the nucleoli were analyzed. A second aim of the study was to identify subcellular components in DHM phase contrast images. Therefore, comparative investigations using bright field imaging, DHM and fluorescence microscopy with 4',6- Diamidino-2-phenylindol (DAPI) staining were performed. DAPI-staining visualizes cell components containing DNA. The obtained results demonstrate exemplarily for two tumor cell lines that from DHM phase contrast images of fixed cells in phosphate buffer saline (PBS) cell thickness values are obtained which are comparable to living cells. Furthermore, it is shown that in many cases nucleus components can be identified only by DHM phase contrast.