κ-卡拉胶邻苯二甲酰基化衍生物的抗氧化活性研究

对κ-卡拉胶进行酸降解得到三种卡拉胶低聚糖,并进一步与苯二甲酰基合成制得三种分子量分别为1450、2520和3430的κ-卡拉胶邻苯二甲酰衍生物(LA、LB和LC)。对产物进行IR表征并对其取代度(DS)进行测定,并检测了产物对羟基自由基.OH、DPPH自由基和过氧化氢的清除活性以及还原能力。结果表明,上述三种κ-卡拉胶邻苯二甲酰衍生物的抗氧化能力强弱顺序依次为:LC〉LA〉LB,这可能与衍生物的羟基含量、取代基团的性质以及取代度等因素有关。...

Full description

Saved in:
Bibliographic Details
Published in天然产物研究与开发 Vol. 23; no. 3; pp. 530 - 533
Main Author 孙涛 陶慧娜 周冬香 毛芳 谢晶
Format Journal Article
LanguageChinese
Published 上海海洋大学食品学院,上海,201306 2011
Subjects
Online AccessGet full text
ISSN1001-6880
DOI10.3969/j.issn.1001-6880.2011.03.032

Cover

More Information
Summary:对κ-卡拉胶进行酸降解得到三种卡拉胶低聚糖,并进一步与苯二甲酰基合成制得三种分子量分别为1450、2520和3430的κ-卡拉胶邻苯二甲酰衍生物(LA、LB和LC)。对产物进行IR表征并对其取代度(DS)进行测定,并检测了产物对羟基自由基.OH、DPPH自由基和过氧化氢的清除活性以及还原能力。结果表明,上述三种κ-卡拉胶邻苯二甲酰衍生物的抗氧化能力强弱顺序依次为:LC〉LA〉LB,这可能与衍生物的羟基含量、取代基团的性质以及取代度等因素有关。
Bibliography:Three κ-carrageenan oligosaccharides were prepared by acidic degradation of κ-carrageenan.Their phthaloyl derivatives with different molecular weight(LA∶1450;LB∶2520;LC∶3430) were synthesized with phthalic anhydride.The products were characterized by FI-IR,and the degrees of acylation(DS) were determined.Their antioxidant activities were evaluated by the scavenging of hydroxyl radical,1,1-diphenyl-2-picrylhrazyl radicals (DPPH),hydrogen peroxide and reducing power.The results indicated that the orders of antioxidant activities were:LC LA LB.It may be related to the content of hydroxyl groups,the nature of substituting group and the substituting degrees.
SUN Tao,TAO Hui-na,ZHOU Dong-xiang,MAO Fang,XIE JingCollege of Food Science,Shanghai Ocean University,Shanghai 201306,China
κ-carrageenan; acid degradation; phthaloyl; antioxidant activity
51-1335/Q
ISSN:1001-6880
DOI:10.3969/j.issn.1001-6880.2011.03.032