Online RP-HPLC-DPPH screening method for detection of radical-scavenging phytochemicals from flowers of Acacia confusa

被引:80
作者
Wu, Jyh-Horng [3 ]
Huang, Chih-Yu [1 ,2 ]
Tung, Yu-Tang [1 ,2 ]
Chang, Shang-Tzen [1 ,2 ]
机构
[1] Natl Taiwan Univ, Sch Forest Resources & Conservat, Taipei 106, Taiwan
[2] Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan
[3] Natl Chung Hsing Univ, Dept Forestry, Taichung 402, Taiwan
关键词
Acacia confusa; flower extract; radical-scavenging activity; online RP-HPLC-DPPH; antioxidant;
D O I
10.1021/jf072314c
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Acacia confusa is traditionally used as a medicinal plant in Taiwan. In this study, phytochemicals and antioxidant activities of extracts from flowers of A. confusa were investigated for the first time. In addition, a rapid screening method, online RP-HPLC-DPPH system, for individual antioxidants in complex matrices was developed. Accordingly, six antioxidants including gallic acid (1), myricetin 3-rhamnoside (2), quercetin 3-rhamnoside (3), kaempferol 3-rhamnoside (4), europetin 3-rhamnoside (5), and rhamnetin 3-rhamnoside (6) were detected using the developed screening method. Of these, compounds 2, 3, and 5 were found to be major bioactive phytochemicals, and their contents were determined as 11.3, 6.7, and 8.7 mg/g of crude extract, respectively. By comparison with quercetin, a well-known antioxidant, these compounds had the order of compound 2 > compound 5 > quercetin > compound 3 for DPPH radical-scavenging activity. Their IC50 values were 3.0, 3.2, 4.5, and 7.4,mu M, respectively. Moreover, the same order was observed for superoxide radical-scavenging activity, and their IC50 values were 2.6, 2.7, 4.3, and 5.3 mu M, respectively. However, for lipid peroxidation, quercetin, an aglycon, showed the best inhibitory activity. The IC50 values of quercetin, compound 2, compound 5, and compound 3 were 46.7, 88.5, 90.7, and 124.6 mu M, respectively. These results indicated that a rhamnoside at the C3 position of flavonoids had a negative effect on radical-scavenging activity and antilipid peroxidation. In contrast, the number of hydroxyl groups on the B-ring exhibited a positive relationship with their inhibitory activities.
引用
收藏
页码:328 / 332
页数:5
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