食品科学 ›› 2009, Vol. 30 ›› Issue (14): 114-118.doi: 10.7506/spkx1002-6630-200914018

• 工艺技术 • 上一篇    下一篇

红薯叶黄酮分离纯化工艺及抗氧化性研究

陆 英1,2,吴朝比2,蒋华军2,罗 巍2,廖红梅2,刘仲华1,2,*   

  1. 1.湖南农业大学天然产物研究中心 2.湖南农业大学园艺园林学院植物资源工程系
  • 收稿日期:2008-11-07 修回日期:2009-01-15 出版日期:2009-07-15 发布日期:2010-12-29
  • 通讯作者: 刘仲华1,2,* E-mail:larkin-liu@163.com

Extraction, Purification and Antioxidation of Total Flavonoids from Sweet Potato Leaves

LU Ying1,2,WU Chao-bi2,JIANG Hua-jun2,LUO Wei2,LIAO Hong-mei2,LIU Zhong-hua1,2,*   

  1. 1. Research Center of Natural Products, Hunan Agricultural University, Changsha 410128, China;2. Department of Herb Resource
    Engineering, College of Horticulture and Landscape, Hunan Agricultural University, Changsha 410128, China
  • Received:2008-11-07 Revised:2009-01-15 Online:2009-07-15 Published:2010-12-29
  • Contact: LIU Zhong-hua1,2,* E-mail:larkin-liu@163.com

摘要:

本实验以红薯叶为原料,研究了黄酮类化合物分离纯化工艺,并研究了粗提物与纯化产物对羟基自由基、1,1- 二苯基-2- 苦基肼自由基(OPPH·)的清除作用。结果表明,红薯叶黄酮最佳提取工艺为60% 乙醇水溶液90℃回流提取60min,料液比1:40,粗提物中总黄酮含量为101.3mg/g。提取液用HPD500 大孔树脂进行纯化效果好,最佳纯化工艺为:吸附条件:上样原料液黄酮含量1.8mg/ml,pH3 上样流速为3BV/h;洗脱条件:50% 乙醇、流速3BV/h,流量4BV,在此条件下,纯化产品黄酮含量为488.7mg/g;粗提物与纯化产物均具有对自由基的清除作用,是一种有效的天然抗氧化剂新资源。

关键词: 红薯叶, 黄酮, HPD500大孔树脂, 分离纯化, 抗氧化性

Abstract:

Except that few sweet potato leaves are taken as edible food or livestock feed, most of them that contain large amounts of bioactive flavonoids are discarded, which leads to a great waste of available resource. In the present study total flavonoids were extracted from sweet potato leaves using ethanol and purified using macroporous adsorption resin. The extraction and purification procedures were optimized by orthogonal array design and one-factor-at-a-time methods, respectively. Additionally, antioxidant properties of the purified total flavonoids were evaluated by assaying their ·OH and DPPH· scavenging activities. The optimal extraction conditions were as follows: ethanol concentration 60%, material/liquid 1:40, and temperature 90 ℃ for a thermal refluxing extraction duration of 60 min, and 1 g of the crude extract obtained under such conditions contained 101.3 mg of total flavonoids. The optimal purification parameters using macroporous resin HPD 500 whose adsorption and desorption performance was superior to those of other resins including AB-8, NKA-9, HPD 600 and HPD 450 were as follows: sample concentration 1.8 mg/ml, pH 3, and sample flow rate 3 BV/h; taking 50% ethanol as eluent, eluent flux 3 BV/h, and eluent quantity 4 BV, and the content of total flavonoids in the purified extract was 488.7 mg/g. Both of the crude extract and the purified product displayed a good scavenging activity to ·OH and DPPH·

Key words: sweet potato leaves, flavonoids, HPD500 resin, extraction and purification, antioxidant activity

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