General Phenolic Analysis
The chromatographic peaks present in each sample were evaluated
spectrophometrically to determine the class of phenolic compoundsflavonoid,
coumarin/cinnamic acid, or psoralinto which the peak belonged.
This information was used to construct table
2, which summarizes the overall phenolic composition for each
species examined.
Data Collection. For each discernible phenolic peak
on the HPLC run trace at 285 nm examined, a spectrum and a relative
retention time was obtained, and then it was classified as either
one of the three classes of phenolics or an unknown. During the
HPLC run, diode array absorption spectra were taken of each detectable
peak at three points as it passed through the detector: up-slope,
apex, and down-slope. This information was retrieved from the
computer, and the peak apex spectrum was printed out on the plotter
for each peak. The up- and down-slope spectra were examined if
there was any ambiguity in assigning peaks to classes.
Purified standards, either isolated in this laboratory or purchased
from chemical supply companies, were used to determine both a
characteristic absorbance spectrum for each of the four classes
of phenolics examined and their extinction coefficients at 285
nm. The characteristic spectra of standards of these compounds
are shown in figure 2. Peaks
from sample runs were then assigned a classification based on
the following spectral criteria:
Flavanones. Flavanones are identifiable by a characteristic
absorbance maximum at 280288 nm and a broad shoulder at
about 330 nm (figure 2). These
features, as well as the large number of known spectra, were used
to identify this class of compounds.
Flavones and Flavonols. Flavones and flavonols exhibit
high absorbances in both the 240270 nm region and the 320380
nm region. The flavonones and flavonols have very similar spectra
and it is difficult to differentiate between the two types of
compounds based on spectra alone, so they are classified together
here.
Coumarins and Cinnamic Acids. As a class, coumarins
are identified on the basis of their characteristically large
absorbance peak occurring in the region of 310330 nm (figure 2). Cinnamic acid derivatives
(including pcoumaric acid, caffeic acid, and ferulic
acid), although they are distinct compounds and somewhat distant
biosynthetically, are included in this class because of the similarity
of their absorbance spectra to that of the coumarins. Cinnamic
acid derivatives are present in relatively high concentrations
in mature grapefruit (Maier and Metzler
1967).
Psoralens. Psoralens (furocoumarins) have been isolated
from many citrus species. They are identifiable by absorbance
maxima in the region of 240265 nm, followed by a precipitous
dip in the region of 270290 nm, and a broader, smaller peak
in the region of 320350 nm (figure
2).
Unknown. Unknowns comprised those compounds that absorbed
light at 285 nm but were either obvious mixtures of compounds
(as determined by the examination of the up-slope and down-slope
spectra of these peaks) or had a spectrum that did not match that
of the four general classes outlined above.
After the peaks in a given sample were identified, the relative
concentrations of each class in the sample were determined. The
concentrations were ascertained from peak areas printed out by
the computer in milliabsorbance units, using the extinction coefficients
determined from the standards.
United States
Department of Agriculture
Agricultural
Research Service
The material on this page is in the public
domain.
Original posting: April 1, 1999.
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