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茶多酚微胶囊化的试验研究
引用本文:孟祥,李保国.茶多酚微胶囊化的试验研究[J].茶叶科学,2006,26(4):275-279.
作者姓名:孟祥  李保国
作者单位:上海理工大学低温医学与食品生物技术研究所,上海,200093;上海理工大学低温医学与食品生物技术研究所,上海,200093
基金项目:上海市自然科学基金;上海市重点学科建设项目;上海市联盟计划-难题攻关项目
摘    要:采用喷雾干燥法,以生物可降解高分子材料羟丙基甲基纤维素邻苯二甲酸酯(HPMCP)为骨架材料,对茶多酚进行微胶囊化研究。以微球的包封率作为实验指标,用L9 (34)正交实验设计优化制备茶多酚微球的工艺,得到以下结果:加入少量乳化剂可较大程度提高产品的包封率,十二烷基硫酸钠(SDS)作为乳化剂效果比聚乙烯醇(PVA)好,最佳添加量是芯壁材总重的4%;制备茶多酚缓释微球的最佳条件为:进风温度100℃,进料速度6.25βml/min,芯壁材比为2:1,总固形物含量为3%。采用HPMCP作为壁材,以喷雾干燥法对茶多酚进行微胶囊化是可行的,茶多酚微球有一定的缓释效果。

关 键 词:喷雾干燥  茶多酚  微球  羟丙基甲基纤维素邻苯二甲酸酯
文章编号:1000-369X(2006)04-275-05
收稿时间:2005-03-15
修稿时间:2006-09-06

Experimental study on Microencapsulation of Tea Polyphenols
MENG Xiang,LI Bao-guo.Experimental study on Microencapsulation of Tea Polyphenols[J].Journal of Tea Science,2006,26(4):275-279.
Authors:MENG Xiang  LI Bao-guo
Institution:Institute of Food & biological technology, University of Shanghai for science and technology, Shanghai 200093,China
Abstract:To explore the new method of preparing slow-releasing microspheres of tea polyphenols, which will be useful for the applications of tea polyphenols. Through spray drying technology, tea polyphenols were microencapsulated by hydroxypropyl methylcellulose phthalate which is a biodegradable material. The microencapsulation process of tea polyphenols was optimized with orthogonal design L9 (34), the retention of tea polyphenols microspheres was used as the index. Results: A little emulsifier could increase the retention greatly , and the efficiency of SDS was better than PVA. The optimized conditions of tea polyphenols microencapsulation were that entrance temperature was 100℃, entrance speed was 6.25 ml/min, proportion of tea polyphenols and wall material was 2:1, proportion of all solid maters was 3%. Using Hydroxypropyl methylcellulose phthalate as the wall material is feasible to prepare tea polyphenols microspheres by spray drying technology, and tea polyphenols microspheres had a slow-releasing efficiency.
Keywords:spray drying  tea polyphenols  microsphere  hydroxypropyl methylcellulose phthalate
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