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• W2887477202 abstract "Living cells are highly dynamic systems responding to a large variety of biochemical and mechanical stimuli over minutes, which are well controlled by e.g. optical tweezers. However, live cell investigation through fluorescence microscopy is usually limited not only by the spatial and temporal imaging resolution but also by fluorophore bleaching. Therefore, we designed a miniature light-sheet illumination system that is implemented in a conventional inverted microscope equipped with optical tweezers and interferometric tracking to capture 3D images of living macrophages at reduced bleaching. The horizontal light-sheet is generated with a 0.12 mm small cantilevered mirror placed at 45° to the detection axis. The objective launched illumination beam is reflected by the micro-mirror and illuminates the sample perpendicular to the detection axis. Lateral and axial scanning of both Gaussian and Bessel beams, together with an electrically tunable lens for fast focusing, enables rapid 3D image capture without moving the sample or the objective lens. Using scanned Bessel beams and line-confocal detection, an average axial resolution of 0.8 µm together with a 10-15 fold improved image contrast is achieved." @default.
• W2887477202 created "2018-08-22" @default.
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• W2887477202 date "2018-08-14" @default.
• W2887477202 modified "2023-10-18" @default.
• W2887477202 title "Miniature scanning light-sheet illumination implemented in a conventional microscope" @default.
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• W2887477202 doi "https://doi.org/10.1364/boe.9.004263" @default.
• W2887477202 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6157761" @default.
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