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CHMELÍK, R., HARNA, Z.
Original Title
Parallel-Mode Confocal Microscopy
Type
journal article - other
Language
English
Original Abstract
Conventional confocal microscopes are based on the dual scanning of a specimen by the images of a point source and of a point detector. Hence, their imaging mode is serial, i.e., the confocal image is obtained from the sequence of single-point or multiple-point partial images. Parallel-mode confocal imaging is possible on the basis of broad-source image-plane holography. We adapted this classical-holography technique for real-time reflected-light microscopy. The imaging speed of the parallel-mode confocal microscope is not limited by any part of the optical system, but only by the image detection and storage systems. Both the image phase and the image amplitude are reconstructed from the interference signal. It was verified both theoretically and experimentally that the main imaging parameters of the microscope are comparable with those of a conventional confocal microscope. The only exception is the imaging speed, which can be much higher.
Keywords
Confocal microscopy, Holographic applications, Real-time imaging.
Authors
RIV year
2001
Released
1. 1. 1999
ISBN
0091-3286
Periodical
Optical Engineering
Year of study
38
Number
10
State
United States of America
Pages from
1635
Pages to
1639
Pages count
5
BibTex
@article{BUT39686, author="Radim {Chmelík} and Zdeněk {Harna}", title="Parallel-Mode Confocal Microscopy", journal="Optical Engineering", year="1999", volume="38", number="10", pages="5", issn="0091-3286" }