应用化学 ›› 2016, Vol. 33 ›› Issue (7): 827-833.DOI: 10.11944/j.issn.1000-0518.2016.07.150352

• 研究论文 • 上一篇    下一篇

β-环糊精及衍生物与β-胡萝卜素包合物性质

周叶红a,马学文a,梁文婷a,董川a*(),双少敏b*()   

  1. a 山西大学 环境科学研究所 太原 030006
    b 山西大学 化学与化工学院 太原 030006
  • 收稿日期:2015-10-08 接受日期:2016-01-06 出版日期:2016-06-30 发布日期:2016-06-30
  • 通讯作者: 董川,双少敏
  • 基金资助:
    国家自然科学基金资助项目(21575084)

Preparation and Physicochemical Properties of the Inclusion Complexes of β-Carotene with β-Cyclodextrin and Its Derivatives

ZHOU Yehonga,MA Xuewenb,LIANG Wentingb,DONG Chuanb*(),SHUANG Shaomina*()   

  1. a Institute of Environmental Science,Shanxi University,Taiyuan 030006,China
    b School of Chemistry and Chemical Engineering,Shanxi University,Taiyuan 030006,China
  • Received:2015-10-08 Accepted:2016-01-06 Published:2016-06-30 Online:2016-06-30
  • Contact: DONG Chuan,SHUANG Shaomin
  • Supported by:
    Supported by the National Natural Science Foundation of China(No.21575084)

摘要:

为了改善β-胡萝卜素的理化性质,如水溶性和光稳定性等,分别制备了β-胡萝卜素与β-环糊精、2-羟丙基-β-环糊精、磺丁基醚-β-环糊精的固体包合物。 利用紫外-可见吸收光谱、傅里叶红外转换光谱和核磁技术对β-胡萝卜素与环糊精及其衍生物的包合物进行研究。 通过对包合物理化性质的研究发现:通过β-环糊精、2-羟丙基-β-环糊精、磺丁基醚-β-环糊精包合后的β-胡萝卜素的理化性质,包括热稳定性、光稳定性和抗氧化性,均有显著提高;经2-羟丙基-β-环糊精和磺丁基醚-β-环糊精包合后,β-胡萝卜素分别增溶12倍和18倍。

关键词: β-胡萝卜素, 环糊精, 水溶性, 包合物, 稳定性

Abstract:

The solid inclusion complexes of β-carotene with β-cyclodextrin, 2-hydroxypropyl-β-cyclodextrin and sulfobutylether-β-cyclodextrin were prepared in order to improve physicochemical properties of β-carotene, such as solubility and stability. The inclusion complexes of β-carotene with β-cyclodextrin and its derivatives were characterized by UV-Vis absorption spectroscopy, Fourier-transform infrared spectroscopy and 1H NMR spectroscopy. The physicochemical properties of inclusion complexes indicate that the heat stability, light stability and antioxidant activity of β-carotene are evidently improved by the formation of inclusion complexes of β-carotene with β-cyclodextrin, 2-hydroxypropyl-β-cyclodextrin and sulfobutylether-β-cyclodextrin, respectively. The solubility of β-carotene increases 12 times and 18 times by the formation of inclusion complexes of β-carotene with 2-hydroxypropyl-β-cyclodextrin and sulfobutylether-β-cyclodextrin, respectively.

Key words: β-carotene, cyclodextrins, inclusion complex