Antioxidant activity
Effect of solvents on DPPH radical scavenging activity
DPPH free-radical scavenging method is based on the
exchange of hydrogen atoms between the antioxidant and
the stable DPPH free radical. The used synthetic-free radi-
cals are DPPH. This compound reacts with antioxidant
compounds by taking hydrogen atoms from antioxidant
compounds and getting electron pairs. When an antioxi-
dant encounters the DPPH solution, the color changes from
purple to yellow due to its scavenging action on free radi-
cal. The color change of DPPH solution in the presence of
extracts was measured at 517 nm spectrophotometrically
[
29
]. A lower absorption spectrum intensity shows a higher
DPPH radical-scavenging activity. Figure
1
illustrates
DPPH radical scavenging of various extracts obtained by
extraction of powdered onion skin at concentrations rang-
ing from 6.25 to 100 μg/mL. The results depict the DPPH
scavenging activities of the extracts in a concentration-
dependent manner. The IC
50
values of the extracts were
20.926 ± 0.41, 21.738 ± 0.43, 22.447 ± 0.59, 24.48 ± 0.64
and 36.111 ± 0.86 μg/mL for ethyl acetate, n-butanol, etha-
nol, methanol and distilled water, respectively. The extract
obtained by ethyl acetate yielded the highest DPPH radical
scavenging activity. IC
50
values of the extracts demonstrated
the noticeable antioxidant activity, comparable to that of
BHA (51.43 ± 0.70 μg/mL). In general, the results showed
that all the prepared extracts have the ability to scavenge
free radicals. This finding is in agreement with the results
reported by Singh et al. [
15
] and Skerget et al. [
25
] which
showed that the antioxidant and radical scavenging activities
of red onion skin extracts were commonly high, compara-
ble to that of BHA. However, extracts acquired by organic
solvents provided stronger radical scavenging capacity than
that of distilled water.
Moreover, our results show that DPPH radical scaveng-
ing activity has high correlation with total flavonoid content
(R = 0.9468). Lower correlation was observed between this
activity and total phenolic contents (R = 0.8908). Solvents
polarity and its effect on extraction of phenol and flavonoids
are mainly responsible for differences between the DPPH
radical scavenging capacities of the extracts. The capacity of
phenolic and flavonoid compounds to scavenge free radicals
may be due to the presence of the hydroxyl groups in their
structure and their electron donating ability which transfer
hydrogen to radicals and produce phenoxide radical to sta-
bilize products.
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