Antioxidant effects of various solvent extracts from Ampelopsis japonica determined by DPPH, ABTS, superoxide radical scavenging, and FRAP assays.

Antioxidant effects of various solvent extracts from Ampelopsis japonica determined by DPPH, ABTS, superoxide radical scavenging, and FRAP assays.

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The dried root of Ampelopsis japonica (Thunb.) Makino (A. japonica.) is a traditional medicine used to treat fever, pain, and wound healing. It exhibits anti-inflammatory, antitumor, antityrosinase, and antimelanogenic activities. In this paper, we used different solvent extracts from the root of A. japonica to determine their antioxidant activity....

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Context 1
... acetone extract (SC 50 = 54.88 ± 4.04 µg/mL) showed strong DPPH radical scavenging activity, followed by methanol (SC 50 = 84.73 ± 7.82 µg/mL), ethanol (SC 50 = 87.12 ± 6.45 µg/mL), ethyl acetate (SC 50 = 92.14 ± 8.12 µg/mL), and water (SC 50 = 98.54 ± 7.09 µg/mL), as shown in Table 2. In addition, the extracts of n-hexane, chloroform, and dichloromethane had no significant effect (SC 50 > 200 µg/mL). ...
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... 4.74 µg/mL), ethanol (SC 50 = 64.56 ± 4.80 µg/mL), and water (SC 50 = 99.30 ± 7.02 µg/mL), as shown in Table 2. In addition, dichloromethane, chloroform, and n-hexane extracts had no significant effect (SC 50 > 200 µg/mL). ...
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... the result in Table 2, all extracts of A. japonica were tested for their superoxide radical scavenging activity. Notably, the results exhibited that, except for methanol (SC 50 = 290.83 ...
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... 20.61 TE mM/g), and water (413.34 ± 21.08 TE mM/g) in Table 2. The solvent extracts with low polarities, such as dichloromethane, chloroform, and n-hexane, showed relatively weak FRAP values. ...

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... Radical scavenging activity (%) = (Abscontrol − Abssample)/Abscontrol × 100 2.4.2. Measurement of ABTS Cation Radical Scavenging Activity ABTS cation radical scavenging ability was measured using Liang et al.'s method, with slight modifications [17]. The reaction of an equal volume of 7 mM ABTS (2,2′-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt) solution with 2.45 mM potassium persulfate in the dark for 18 h produced an ABTS cationic radical. ...
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... At a concentration of 1 mg/mL, compounds 3 and 8 were singled out as the most potent inhibitors of the AChE with high percentages of inhibition (>68%, Figure 3) which were comparable to the activity of donepezil (a commercial drug). Compound 3, a natural organic acid which distributed widely in natural organisms, was also found to be an efficient AChEi in the previous reports [26][27]. Interestingly, as analogues of 3, compounds 4 and 5 showed weak inhibitory activity, indicating that the free carboxyl group on the benzene ring is 24 crucial for AChE inhibitory activity. ...
... The ABTS stock solution was reacted with 7 mM potassium persulfate (final concentration), and the mixture was left at room temperature for 12-16 h before use to generate ABTS radicals. Radical scavenging was measured by mixing 200 μL of each sample and 1000 μL ABTS solution [16]. Mixtures were left for 15 min in the dark, and absorbance was measured at 730 nm with the SCINCO UV-Vis spectrophotometer S-3100 (Seoul, Korea). ...
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