| Literature DB >> 30444085 |
Yong Da Sie1, Chia-Yuan Chang2, Chun-Yu Lin2, Nan-Shan Chang3,4, Paul J Campagnola5, Shean-Jen Chen6.
Abstract
Conventional temporal focusing-based multiphoton excitation microscopy (TFMPEM) can offer widefield optical sectioning with an axial excitation confinement of a few microns. To improve the axial confinement of TFMPEM, a binary computer-generated Fourier hologram (CGFH) via a digital-micromirror-device (DMD) was implemented to intrinsically improve the axial confinement by filling the back-focal aperture of the objective lens. Experimental results show that the excitation focal volume can be condensed and the axial confinement improved about 24% according to the DMD holography. In addition, pseudouniform MPE can be achieved using two complementary CGFHs with rapid pulse-width modulation switching via the DMD. Furthermore, bioimaging of CV-1 in origin with SV40 genes-7 cells demonstrates that the TFMPEM with binary DMD holography can improve image quality by enhancing axial excitation confinement and rejecting out-of-focus excitation. (2018) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE).Entities:
Keywords: fluorescence microscopy; medical and biological imaging; nonlinear microscopy; ultrafast lasers
Mesh:
Year: 2018 PMID: 30444085 DOI: 10.1117/1.JBO.23.11.116502
Source DB: PubMed Journal: J Biomed Opt ISSN: 1083-3668 Impact factor: 3.170