CONFOCAL DIRECT IMAGING RAMAN MICROSCOPE - DESIGN AND APPLICATIONS INBIOLOGY

Citation
Nm. Sijtsema et al., CONFOCAL DIRECT IMAGING RAMAN MICROSCOPE - DESIGN AND APPLICATIONS INBIOLOGY, Applied spectroscopy, 52(3), 1998, pp. 348-355
Citations number
21
Categorie Soggetti
Instument & Instrumentation",Spectroscopy
Journal title
ISSN journal
00037028
Volume
52
Issue
3
Year of publication
1998
Pages
348 - 355
Database
ISI
SICI code
0003-7028(1998)52:3<348:CDIRM->2.0.ZU;2-7
Abstract
A confocal direct imaging Raman microscope (CDIRM) based on two synchr onized scanning mirrors, a monochromator, and two charge-coupled devic e (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 sph ere and a thin layer. The image of a 0.282 mu m sphere appeared to hav e a full width at half-maximum (FWHM) of 1.2 mu m in the axial and 0.3 7 mu m in the lateral direction, whereas the image of a 275 nm layer s howed an FWHW of 1.4 mu m in the axial direction. Confocal Raman image s were made of the DNA and protein distribution in polytene chromosome s with a relatively weak Raman signal [0.1 photons/(second pixel)]. Fu rther, a three-dimensional Raman image of the drug distribution in a p hthalocyanine-incubated fixed cell is presented. These examples show t hat the CDIRM can be used to image samples with a weak Raman signal an d that three-dimensional images of the distribution of specific molecu les in a sample can be made.