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中国精品科技期刊2020
张生生, 闫静芳, 陆兆新, 张丽娟, 武奔月, 陈阳阳, 王昱沣. 锐孔凝固浴法制备表面活性肽微胶囊[J]. 食品工业科技, 2015, (12): 221-225. DOI: 10.13386/j.issn1002-0306.2015.12.038
引用本文: 张生生, 闫静芳, 陆兆新, 张丽娟, 武奔月, 陈阳阳, 王昱沣. 锐孔凝固浴法制备表面活性肽微胶囊[J]. 食品工业科技, 2015, (12): 221-225. DOI: 10.13386/j.issn1002-0306.2015.12.038
ZHANG Sheng-sheng, YAN Jing-fang, LU Zhao-xin, ZHANG Li-juan, WU Ben-yue, CHEN Yang-yang, WANG Yu-feng. The preparation of surfactin microcapsules by the method of piercing-solidifying[J]. Science and Technology of Food Industry, 2015, (12): 221-225. DOI: 10.13386/j.issn1002-0306.2015.12.038
Citation: ZHANG Sheng-sheng, YAN Jing-fang, LU Zhao-xin, ZHANG Li-juan, WU Ben-yue, CHEN Yang-yang, WANG Yu-feng. The preparation of surfactin microcapsules by the method of piercing-solidifying[J]. Science and Technology of Food Industry, 2015, (12): 221-225. DOI: 10.13386/j.issn1002-0306.2015.12.038

锐孔凝固浴法制备表面活性肽微胶囊

The preparation of surfactin microcapsules by the method of piercing-solidifying

  • 摘要: 采用锐孔凝固浴法制备表面活性肽微胶囊,并以海藻酸钠为壁材,氯化钙溶液作为固化液。在单因素的基础上,以包埋率作为评价指标,通过响应面实验对微胶囊制备过程中的氯化钙浓度、芯壁比、海藻酸钠浓度、操作温度四个因素进行优化。结果表明:氯化钙浓度为2%,操作温度为49℃,海藻酸钠与表面活性肽比例为1∶2,海藻酸钠浓度为2.4%时,包埋率达到了87.6%,载药量为12.5%。通过肠液缓释实验发现,微胶囊在9h内的释放率达到了91.7%,具有很好的缓释效果。 

     

    Abstract: In this paper, piercing-solidifying method was applied to obtain the capsules of surfactin with sodium alginate as wall material and calcium chloride as solid solvent. On the basement of one-factor experiments, four factors including calcium chloride and sodium alginate concentration, ratio of core to wall, temperature were optimized by the method of response surface. The performance of all factors was evaluated by the microencapsulation efficiency. The results showed, under the condition of calcium chloride concentration 2%, temperature 49℃, the proportion of sodium alginate to surfactin 1 ∶2, sodium alginate concentration 2.4%, the microencapsulation efficiency reaches 87.6%, the load ratio of drug reaches 12.5%. The release rate of Surfactin from the microcapsule reached 91.7%, which showed that it had good slow-release effect.

     

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