G. Bonnot et G. Febvay, FOURIER PROCESSING OF LIQUID CHROMATOGRAMS USING FLOW RADIOACTIVE DETECTION, Analytical biochemistry, 224(1), 1995, pp. 354-363
Plow radioactivity counters coupled to liquid chromatography devices c
ause a systematic bias to the separation by broadening peaks within th
e radiochromatogram. Such signal smearing may be evaluated on standard
ization runs with a single peak, using the ratio between Fourier trans
forms of whole chromatographic data for the measured radioactivity tim
e series (radioactivity channel) and for the concentration time series
(optical density channel). This ratio constitutes a kernel suitable t
o perform the deconvolution of any radiochromatogram performed under s
imilar conditions. Through deconvolution, the signal smearing is remov
ed, reverting to peaks with the same geometry as in the concentration
chromatogram: same retention time, peak width, and shape. The deconvol
ution method in processing radiochromatograms allows an easier interpr
etation and gives more reliable radioactivity quantification (improved
linearity of the measured response). Fourier transformation of the ra
diochromatogram also allows the removal of transitory events (noise) t
hrough the correlation procedure. This method may provide substantial
gain in sensitivity, depending upon the residence time of the sample i
n the counting cell. (C) 1995 Academic Press, Inc.