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Effects of extraction methods on antioxidants and methoxyflavones of Kaempferia parviflora
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This research was aimed to determine the effects of extraction methods on antioxidant
properties and methoxyflavone contents of Kaempferia parviflora (KP) rhizome extracts.
The KP rhizomes were extracted by maceration using ethanol at the concentrations of 25,
50, 75 and 95% V/V for 7 days and 95% V/V ethanolic extraction with sonication-assisted
extraction (SAE) for 15-45 mins. Antioxidant components (phenolics, flavonoids and
anthocyanins) and antioxidant activities (DPPH and FRAP) were examined.
Methoxyflavones of the KP extracts were identified by a GC-MS technique. It was found
that extraction methods affected the antioxidant properties of the extracts. Increasing
ethanol concentrations enhanced anthocyanins but not phenolics and flavonoids. Ethanol
concentration at 75% V/V exhibited the greatest DPPH while 25% V/V ethanol showed
the greatest FRAP values. In this study, 10 methoxyflavones from KP extracts were
separated and identified by GC chromatograms. The content of 5,7-dimethoxyflavone
increased from 1.1 g/100 mL extract to 48.10 g/100 mL extract as the ethanol
concentrations increased from 25% to 95% V/V. SAE for 15-45 mins had little impact on
antioxidant properties as well as methoxyflavone contents. In general, SAE enhanced the
extraction of KP rhizomes by increasing 5,7-dimethoxyflavone contents.
Title: Effects of extraction methods on antioxidants and methoxyflavones of
Kaempferia parviflora
Description:
This research was aimed to determine the effects of extraction methods on antioxidant
properties and methoxyflavone contents of Kaempferia parviflora (KP) rhizome extracts.
The KP rhizomes were extracted by maceration using ethanol at the concentrations of 25,
50, 75 and 95% V/V for 7 days and 95% V/V ethanolic extraction with sonication-assisted
extraction (SAE) for 15-45 mins.
Antioxidant components (phenolics, flavonoids and
anthocyanins) and antioxidant activities (DPPH and FRAP) were examined.
Methoxyflavones of the KP extracts were identified by a GC-MS technique.
It was found
that extraction methods affected the antioxidant properties of the extracts.
Increasing
ethanol concentrations enhanced anthocyanins but not phenolics and flavonoids.
Ethanol
concentration at 75% V/V exhibited the greatest DPPH while 25% V/V ethanol showed
the greatest FRAP values.
In this study, 10 methoxyflavones from KP extracts were
separated and identified by GC chromatograms.
The content of 5,7-dimethoxyflavone
increased from 1.
1 g/100 mL extract to 48.
10 g/100 mL extract as the ethanol
concentrations increased from 25% to 95% V/V.
SAE for 15-45 mins had little impact on
antioxidant properties as well as methoxyflavone contents.
In general, SAE enhanced the
extraction of KP rhizomes by increasing 5,7-dimethoxyflavone contents.
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