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响应面法优化松多酚微粒制备工艺
引用本文:刁岩,陈斌,王蕊,李桥,赵海田,张华,王路,魏力军,王振宇. 响应面法优化松多酚微粒制备工艺[J]. 食品科学, 2019, 40(6): 281-288. DOI: 10.7506/spkx1002-6630-20180307-081
作者姓名:刁岩  陈斌  王蕊  李桥  赵海田  张华  王路  魏力军  王振宇
作者单位:1.哈尔滨工业大学化工与化学学院,黑龙江 哈尔滨 150001;2.中国航天员科研训练中心 航天营养与食品工程重点实验室,北京 100094;3.哈尔滨工业大学生命科学与技术学院,黑龙江 哈尔滨 150001
基金项目:“十三五”国家重点研发计划重点专项(2016YFC0500305-02);航天营养与食品工程重点实验室航天食品研究基金对外开放课题(SNFEKF1506);国家自然科学基金面上项目(31571798);国家自然科学基金青年科学基金项目(31401483)
摘    要:依据聚电解质自组装原理,利用黑木耳多糖酸性片段(acidic polysaccharide fragments from Auricularia auricula,AAP)和多聚赖氨酸(polylysine,PLL)将松多酚(pine polyphenols from Pinus koraiensis,PPH)包裹为微粒以防止胃环境对多酚类化合物结构的破坏,并且采用响应面试验设计优化制备工艺。通过分析AAP、PLL和PPH的质量浓度3 个因素及其交互作用对PPH微粒包埋率的影响,建立该工艺的二次多项数学模型;利用扫描电镜观察优化后PPH微粒的形貌,并在模拟胃肠道环境中检测多酚释放率。结果显示响应面回归方程拟合性良好,AAP、PLL和PPH的质量浓度对响应值均有显著影响。在AAP质量浓度为900 μg/mL、PPH质量浓度为110 μg/mL以及PLL质量浓度为30 μg/mL的条件下,PPH微粒的包埋率为(86.57±1.07)%,载药量为(24.03±0.81)%。扫描电镜观察表明PPH微粒的直径为200~500 nm,其在模拟胃环境中释放缓慢而在模拟肠道环境中释放迅速。本研究中PPH微粒包埋率的实测值与预测值相比,相对误差较低,说明本研究方法是一种适合PPH微粒制备的方法,并且优化后的PPH微粒可以降低胃环境对PPH的降解。

关 键 词:松多酚  黑木耳多糖  自组装  微粒  响应面  

Optimization of Preparation Process for Pinecone Polyphenol Microparticles by Response Surface Methodology
DIAO Yan,CHEN Bin,WANG Rui,LI Qiao,ZHAO Haitian,ZHANG Hua,WANG Lu,WEI Lijun,WANG Zhenyu. Optimization of Preparation Process for Pinecone Polyphenol Microparticles by Response Surface Methodology[J]. Food Science, 2019, 40(6): 281-288. DOI: 10.7506/spkx1002-6630-20180307-081
Authors:DIAO Yan  CHEN Bin  WANG Rui  LI Qiao  ZHAO Haitian  ZHANG Hua  WANG Lu  WEI Lijun  WANG Zhenyu
Affiliation:1. School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150001, China; 2. Key Laboratory of Space Nutrition and Food Engineering, China Astronauts Research and Training Center, Beijing 100094, China; 3. School of Life Science and Technology, Harbin Institute of Technology, Harbin 150001, China
Abstract:In order to minimize the degradation of pinecone polyphenols in the stomach, pinecone polyphenols from Pinus koraiensis (PPH) were encapsulated by acidic polysaccharide fragments from Auricularia auricula (AAP) and polylysine (PLL) according to the principle of polyelectrolyte self-assembly, and response surface methodology was used to optimize the preparation process. The effect of AAP, PLL and PPH concentration as well as interaction between them on the encapsulation efficiency was evaluated. As a result, a quadratic polynomial model was established describing the process. Scanning electron microscopy (SEM) was used to investigate the morphology of the microparticles prepared under optimized conditions, and the release rate was studied in simulated gastrointestinal environment. The results showed that the fitness of the model was good. All of the three variables had significant effects on the response. The encapsulation efficiency of polyphenol microparticles were (86.57 ± 1.07)% and the drug loading was (24.03 ± 0.81)% at 900 μg/mL AAP, 30 μg/mL PLL and 110 μg/mL PPH concentration. The diameter of the microparticles was 200–500 nm. They were released slowly in simulated gastric environment but rapidly in simulated intestinal environment. The measured encapsulation efficiency matched with the predicted value, indicating that response surface methodology was a suitable method for optimizing the preparation of pinecone polyphenol microparticles. The degradation of pinecone polyphenol microparticles in the stomach environment was decreased relative to free pine polyphenols.
Keywords:pinecone polyphenols  Auricularia auricula polysaccharide  self-assembly  microparticles  response surface methodology  
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