Non-destructive NIR-FT-Raman spectroscopy of plant and animal tissues, of food and works of art

Citation
B. Schrader et al., Non-destructive NIR-FT-Raman spectroscopy of plant and animal tissues, of food and works of art, TALANTA, 53(1), 2000, pp. 35-45
Citations number
35
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
TALANTA
ISSN journal
00399140 → ACNP
Volume
53
Issue
1
Year of publication
2000
Pages
35 - 45
Database
ISI
SICI code
0039-9140(20001002)53:1<35:NNSOPA>2.0.ZU;2-#
Abstract
Just after the discovery of Raman spectroscopy in 1928, it became evident t hat fluorescence with a quantum yield of several orders of magnitude higher than that of the Raman effect was a great and apparently unbeatable compet itor. Raman spectroscopy could therefore, in spite of many exciting advanta ges during the last 60 years, not be applied as an analytical routine metho d: for nearly every sample, fluorescing impurities had to be removed by dis tillation or crystallisation. Purification, however, is not possible for ce lls and tissues, since the removal of the fluorescing enzymes and coenzymes would destroy the cells. There is fortunately one alternative solution. Wh en excited with the radiation of the Nd:YAG laser at 1064 nm Raman spectra are practically free of fluorescence. Raman spectra can now be recorded wit h minimal sample preparation. In order to facilitate non-destructive Raman spectroscopy of any sample, cells and tissues, food, textiles and works of art, a new entrance optics for Raman spectrometers is used. Typical results from several fields are demonstrated. (C) 2000 Elsevier Science B.V. All r ights reserved.