| Literature DB >> 18064238 |
Abstract
We describe a new parallel scanning mechanism for confocal microscopy that is inherently fiber-optic compatible and that retains the simplicity of the line scanning confocal microscope. The method works by employing an incoherent fiber-optic bundle that maps a line illumination pattern back on itself on double passing, while separating the fibers that carry photons from out-of-focus sample planes. The transformation permits efficient rejection of out-of-focus photons by a slit aperture.Year: 2000 PMID: 18064238 DOI: 10.1364/ol.25.000954
Source DB: PubMed Journal: Opt Lett ISSN: 0146-9592 Impact factor: 3.776