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SAGE Publications, Applied Spectroscopy, 3(52), p. 348-355

DOI: 10.1366/0003702981943806

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Confocal Direct Imaging Raman Microscope: Design and Applications in Biology

Journal article published in 1998 by Nanna M. Sijtsema ORCID, Siddi D. Wouters, Cees J. De Grauw, Cees Otto, Jan Greve
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

A confocal direct imaging Raman microscope (CDIRM) based on two synchronized scanning mirrors, a monochromator, and two charge-coupled device (CCD) cameras has been developed. With this system it is possible to make both Raman spectra of a small measurement volume and images of a larger sample area in one specific Raman band. The spatial resolution of the system was determined for two limiting situations: a small sphere and a thin layer. The image of a 0.282 μm sphere appeared to have a full width at half-maximum (FWHM) of 1.2 μm in the axial and 0.37 μm in the lateral direction, whereas the image of a 275 nm layer showed an FWHM of 1.4 μm in the axial direction. Confocal Raman images were made of the DNA and protein distribution in polytene chromosomes with a relatively weak Raman signal [0.1 photons/(second·pixel)]. Further, a three-dimensional Raman image of the drug distribution in a phthalocyanine-incubated fixed cell is presented. These examples show that the CDIRM can be used to image samples with a weak Raman signal and that three-dimensional images of the distribution of specific molecules in a sample can be made.