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.