This study aimed to investigate the effects of wild indigo (Baptisia
tinctoria) root extract as a functional food material, in terms of
antioxidant and skin health-related activities. Both water and ethanol (50/50,
v/v) extracts showed high phenol content. They were evaluated for antioxidant
activity, such as 2,2-diphenyl-1-picrylhydrazyl (DPPH),
2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS),
antioxidant protection factor (PF), and thiobarbituric acid reactive substances
(TBARS). While the DPPH radical scavenging activities of water and ethanol
extracts were 84.23% and 89.30%, respectively, at 200
μg/mL total phenol content (TPC), the ABTS radical
cation scavenging activities were 51.39% and 48.10%, respectively. The water and
ethanol extracts also showed desirable antioxidant PF levels of 1.18 and 1.16,
respectively. Furthermore, the antioxidant effects on TBARS significantly
increased by 37.31% and 51.43%, respectively, in 200
μg/mL of water and ethanol extracts. Both the extracts
showed high dose-dependent collagenase inhibitory activities, up to 27.60% and
77.39%, respectively. The ethanol extract showed an elastase inhibitory activity
of 37.21%; the tyrosinase inhibitory effect (which facilitates natural
skin-whitening) was 59.26% at 200 μg/mL TPC. The
hyaluronidase activity inhibition, related to anti-inflammatory activity, was
20.02% for the water extract and 14.30% for the ethanol extract, at 200
μg/mL TPC. Therefore, B. tinctoria
extract has potential applications in cosmetics and food supplements due to its
antioxidant and skin health promoting activities.
Total phenol content (TPC) of Polyozellus multiplex was the
highest at 97.22±0.91 mg/g when extracted with 70% ethanol. ABTS
radical cation decolorization of both water and 70% ethanol extract
samples was greater than 95.00%. The TBARS inhibition activity of
P. multiplex extracted with 70% ethanol was higher
than that of water extract samples and anti-oxidation activity was identified as
80% or more at 50-200 μg/mL TPC concentration.
The α-glucosidase inhibitory activity of P.
multiplex showed above 85.0% in both water and 70%
ethanol extracts at 150 μg/mL phenolics. Hyaluronidase
inhibitory activity was 46.28% and 27.52% in the water and
70% ethanol extracts at 200 μg/mL TPC
concentration, respectively. The white and red yanggaeng color
values of L, a, and b were all changed with the added extracted powder.
Rheological analysis of hardness, springiness, and chewiness, demonstrated
decreases as the extracted powder content increased. However, as the added
extracted powder increased, cohesiveness was not affected. As a result of the
sensory test, it was determined that for white and red
yanggaeng, the addition of 0.5% (white) and
1.0% or less (red) of the extracted powder is appropriate, respectively.
Considering the intrinsic color of P. multiplex powder
extracts, it is thought that it may be desirable to manufacture it based on red
yanggaeng. Therefore, it was thought that can be expected
biological activities of yanggaeng prepared with P.
multiplex extracted powder.
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