000 01983nam a2200277Ia 4500
003 MX-MdCICY
005 20250625124651.0
040 _cCICY
090 _aB-6921
245 1 0 _aConfocal Direct Imaging Raman Microscope: Design and Applications in Biology
490 0 _vApplied Spectroscopy, 52(3), p.348-355, 1998
520 3 _aA 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 speci® c 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 m m sphere appeared to have a full width at half-maximum (FWHM)of 1.2 m m in the axial and 0.37 m m in the lateral direction, whereas the image of a 275 nm layer showed an FWHM of 1.4 m m 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 hthalocyanine-incubated ® xed 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 speci® c molecules in a sample can be made
650 1 4 _aRAMAN
650 1 4 _aMICROSCOPY
650 1 4 _aSPECTROSCOPY
650 1 4 _aCONFOCAL
650 1 4 _aIMAGING
700 1 2 _aSijtsema, N.M.
700 1 2 _aWouters, S.D.
700 1 2 _aDe Grauw, C.J.
700 1 2 _aOtto, C.
700 1 2 _aGreve, J.
856 4 0 _uhttps://drive.google.com/file/d/1HxzYuPKZWKOIuFXQolb3bxflnZ2aH8-4/view?usp=drivesdk
_zPara ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx
942 _2Loc
_cREF1
008 250602s9999 xx |||||s2 |||| ||und|d
999 _c41258
_d41258