scholarly journals Laser Raman microscope: Application on biological samples.

1990 ◽  
Vol 39 (6) ◽  
pp. 323-334 ◽  
Author(s):  
Yoshifumi NISHIMURA
2012 ◽  
Vol 11 (3) ◽  
pp. 177-186 ◽  
Author(s):  
Sanjoy M. Som ◽  
Bernard H. Foing

AbstractRaman spectrometry has been established as an instrument of choice for studying the structure and bond type of known molecules, and identifying the composition of unknown substances, whether geological or biological. This versatility has led to its strong consideration for planetary exploration. In the context of the ExoGeoLab and ExoHab pilot projects of ESA-ESTEC & ILEWG (International Lunar Exploration Working Group), we investigated samples of astrobiological interest using a portable Raman spectrometer lasing at 785 nm and discuss implications for planetary exploration. We find that biological samples are typically best observed at wavenumbers >1100 cm−1, but their Raman signals are often affected by fluorescence effects, which lowers their signal-to-noise ratio. Raman signals of minerals are typically found at wavenumbers <1100 cm−1, and tend to be less affected by fluorescence. While higher power and/or longer signal integration time improve Raman signals, such power settings are detrimental to biological samples due to sample thermal degradation. Care must be taken in selecting the laser wavelength, power level and integration time for unknown samples, particularly if Raman signatures of biological components are anticipated. We include in the Appendices tables of Raman signatures for astrobiologically relevant organic compounds and minerals.


Author(s):  
W. R. Schucany ◽  
G. H. Kelsoe ◽  
V. F. Allison

Accurate estimation of the size of spheroid organelles from thin sectioned material is often necessary, as uniquely homogenous populations of organelles such as vessicles, granules, or nuclei often are critically important in the morphological identification of similar cell types. However, the difficulty in obtaining accurate diameter measurements of thin sectioned organelles is well known. This difficulty is due to the extreme tenuity of the sectioned material as compared to the size of the intact organelle. In populations where low variance is suspected the traditional method of diameter estimation has been to measure literally hundreds of profiles and to describe the “largest” as representative of the “approximate maximal diameter”.


Author(s):  
C. F. Oster

Although ultra-thin sectioning techniques are widely used in the biological sciences, their applications are somewhat less popular but very useful in industrial applications. This presentation will review several specific applications where ultra-thin sectioning techniques have proven invaluable.The preparation of samples for sectioning usually involves embedding in an epoxy resin. Araldite 6005 Resin and Hardener are mixed so that the hardness of the embedding medium matches that of the sample to reduce any distortion of the sample during the sectioning process. No dehydration series are needed to prepare our usual samples for embedding, but some types require hardening and staining steps. The embedded samples are sectioned with either a prototype of a Porter-Blum Microtome or an LKB Ultrotome III. Both instruments are equipped with diamond knives.In the study of photographic film, the distribution of the developed silver particles through the layer is important to the image tone and/or scattering power. Also, the morphology of the developed silver is an important factor, and cross sections will show this structure.


Author(s):  
Patrick Echlin

A number of papers have appeared recently which purport to have carried out x-ray microanalysis on fully frozen hydrated samples. It is important to establish reliable criteria to be certain that a sample is in a fully hydrated state. The morphological appearance of the sample is an obvious parameter because fully hydrated samples lack the detailed structure seen in their freeze dried counterparts. The electron scattering by ice within a frozen-hydrated section and from the surface of a frozen-hydrated fracture face obscures cellular detail. (Fig. 1G and 1H.) However, the morphological appearance alone can be quite deceptive for as Figures 1E and 1F show, parts of frozen-dried samples may also have the poor morphology normally associated with fully hydrated samples. It is only when one examines the x-ray spectra that an assurance can be given that the sample is fully hydrated.


1981 ◽  
Vol 42 (C4) ◽  
pp. C4-903-C4-906 ◽  
Author(s):  
A. P. Firth ◽  
A. E. Owen ◽  
P. J. Ewen
Keyword(s):  

1984 ◽  
Vol 45 (C2) ◽  
pp. C2-249-C2-253 ◽  
Author(s):  
P. Dhamelincourt ◽  
J. Barbillat ◽  
M. Delhaye
Keyword(s):  

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