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作 者:杨小兰[1] 郑海鹰[1] 胡仕屏[1] 罗正明[1] 张晓云[2]
机构地区:[1]山西大学生命科学与技术学院,山西太原030006 [2]山西医科大学第一医院呼吸科,山西太原030001
出 处:《食品科学》2008年第11期137-141,共5页Food Science
基 金:山西省自然科学基金项目(2006011019);太原市大学生创新创业计划项目(08122014)
摘 要:通过单因素和正交试验确定了啤酒花CO2萃余物中总黄酮的最佳提取条件:浸提剂50%乙醇,料液比1:25(g/ml),回流提取温度70℃,提取时间2.5h,在此条件下总黄酮的提取量为68.09mg/g干酒花。抗氧化实验结果显示提取的啤酒花总黄酮对DPPH自由基的清除能力(IC505.73μg/ml)优于抗坏血酸(IC508.79μg/ml)和芦丁(IC5014.84μg/ml);啤酒花总黄酮的还原力(EC500.158mg/ml),优于芦丁(EC500.252mg/ml),弱于抗坏血酸(EC500.103mg/ml);啤酒花总黄酮对小鼠肝匀浆Fe2++H2O2诱导脂质过氧化产生丙二醛(MDA)的抑制能力(IC500.517mg/ml)优于芦丁(IC500.596mg/ml),表明啤酒花总黄酮具有显著的抗氧化活性。The extraction technology of total flavonoids from supercritical CO2 extraction residue ofHumulus lupulus was optimized by using singel factor and orthogonal test. The optimal extraction conditions are determined as follows: 50% ethanol as extraction solvent, the ratio of materiel to 50% ethanol 1: 25(g/ml), circumfluence temperature 70℃, and circumfluence time 2.5 h, and extraction rate reaches 68.09 mg/g dry Humulus lupulus under the above conditions. The results ofantioxidative experiment showed that the flavonoids extracts has stronger DPPH freed radical scavenging activity (IC50 5.73 μg/ml) than ascorbic acid (IC50 8.79 μg/ml ) and rutin(14.84 μg/ml), and it has stronger reducing capacity (EC50 0.158 mg/ml) than rutin (0.252 mg/ml), but weaker than ascorbic acid (0.103 mg/ml); It also has stronger inhibition rate on MDA produced by lipideroxidation induced by Fe^2+-H2O2 in mouse liver homogenate than rutin. As a conclusion, the total flavonoids from supercritical CO2 extraction residue ofHumulus lupulus has strong antioxdant capacity.
关 键 词:超临界CO2萃余物 啤酒花总黄酮 提取工艺 DPPH自由基 还原力 脂质过氧化
分 类 号:TS218[轻工技术与工程—粮食、油脂及植物蛋白工程]
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