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首页> 外文期刊>Comparative biochemistry and physiology. Toxicology & pharmacology: CBP >Antioxidant activity of different species and varieties of turmeric (Curcuma spp): Isolation of active compounds
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Antioxidant activity of different species and varieties of turmeric (Curcuma spp): Isolation of active compounds

机译:姜黄(Curcuma SPP)不同种类和品种品种的抗氧化活性:活性化合物的分离

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摘要

There are 80 species of turmeric (Curcuma app.) and some species have multiple varieties, for example, Curcuma longa (C. longa) has 70 varieties. They could be different in their chemical properties and biological activities. Therefore, we compared antioxidant activity, total phenolic and flavonoid content of different species and varieties of turmeric namely C. longa [variety: Ryudai gold (RD) and Okinawa ukon], C. xanthorrhiza, C. aromatica, C. amada, and C. zedoaria. The antioxidant activity was determined using the 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging activity, oxygen radical absorbance capacity (ORAC), reducing power and 2-deoxyribose (2-DR) oxidation assay. Our results suggested that RD contained significantly higher concentrations of total phenolic (157.4 mg gallic acid equivalent/g extract) and flavonoids (1089.5 mg rutin equivalent/g extract). RD also showed significantly higher DPPH radical-scavenging activity (IC50: 26.4 mu g/mL), ORAC (14,090 mu mol Trolox equivalent/g extract), reducing power absorbance (0.33) and hydroxyl radical scavenging activity (IC50: 7.4 mu g/mL). Therefore, RD was chosen for the isolation of antioxidant compounds using silica gel column, Toyopearl HW-40F column, and high-performance liquid chromatography. Structural identification of the compounds was conducted using H-1 NMR, C-13 NMR, and liquid chromatography-tandem mass spectrometry. The purified antioxidant compounds were bisabolone-9-one (1), 4-methyllene-5-hydroxybisabola-2,10-diene-9-one (2), turmeronol B (3), 5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)-1-hepten-3-one (4), 3-hydroxy-1,7-bis(4-hydroxyphenyl)-6-hepten-1,5-dione (5), cyclobisdemethoxycurcumin (6), bisdemethoxycurcumin (7), demethoxycurcumin (8) and curcumin (9). The IC50 for DPPH radical-scavenging activity were 474, 621, 234, 29, 39, 257, 198, 47 and 18 mu M and hydroxyl radical-scavenging activity were 25.1, 24.4, 20.2, 2.1, 5.1, 17.2, 7.2, 3.3 and 1.5 mu M for compound 1, 2, 3, 4, 5, 6, 7, 8 and 9, respectively. Our findings suggested that the RD variety of C. longa, developed by the University of the Ryukyus, Okinawa, Japan, is a promising source of natural antioxidants.
机译:有& 80种姜黄(Curcuma App.)和一些物种具有多种品种,例如Curcuma Longa(C. longa)有70个品种。它们在其化学性质和生物活动中可能是不同的。因此,我们比较了抗氧化活性,不同种类和品种的姜黄和黄酮类化合物含量的抗氧化活性,即姜黄,即C. longa [品种:Ryudai Gold(Rd)和冲绳乌隆],C. Xanthorrhiza,C. Aromatica,C.Amada和C. 。Zedoaria。使用1,1-二苯基-2-富铬酰肼(DPPH)自由基清除活性,氧自由基吸收能力(ORAC),降低功率和2-脱氧(2-DR)氧化测定测定抗氧化活性。我们的研究结果表明,RD含有显着较高的总酚醛(157.4mg Gallic酸当量/ G.提取物)和黄酮类化合物(1089.5mg牛丁类药物/ g提取物)。 RD还显示出明显较高的DPPH自由基清除活性(IC50:26.4μg/ ml),orac(14,090μmolrotox当量/ g提取物),降低功率吸收(0.33)和羟基自由基清除活性(IC50:7.4μg/ ml)。因此,选择使用硅胶柱,Toyopearl HW-40F柱和高性能液相色谱分离抗氧化化合物的RD。使用H-1 NMR,C-13 NMR和液相色谱 - 串联质谱法进行化合物的结构鉴定。纯化的抗氧化剂化合物是双式酮-9-一(1),4-甲基丙烯-5-羟基比巴醇-2,10-二烯-9-一(2),Turmeronolb(3),5-羟基-1,7-Bis (4-羟基-3-甲氧基苯基)-1-庚酮-3-一(4),3-羟基-1,7-双(4-羟基苯基)-6-庚烷-1,5-二酮(5),环二甲氧基核蛋白(6),双甲氧键菌蛋白(7),去甲氧杂环蛋白(8)和姜黄素(9)。对于DPPH自由基活性的IC 50为474,621,234,29,39,257,198,47和18μm和羟基自由基清除活性为25.1,20.4,20.2,2.1,5.1,17.2,7.2,3.3对于化合物1,2,3,4,5,6,7,8和9分别为1.5μm。我们的研究结果表明,日本冲绳大学的Ryukyus大学开发的C. Longa的RD多样性是天然抗氧化剂的有希望的来源。

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