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Preparation, characterization, water solubility, and targeted delivery of linear dextrin-conjugated linoleic acid inclusion complex

机译:线性糊精偶联的亚油酸包合物的制备,表征,水溶性和靶向递送

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摘要

A linear dextrin (LD)-conjugated linoleic acid (CLA) inclusion complex was prepared using LD obtained from debranched waxy corn starch as an encapsulation wall material. The aim was to prepare a nontoxic CLA product with improved water solubility and controlled release in small intestine by encapsulating CLA with the water-soluble LD. The optimal complexation temperature, volume of ethanol used to dissolve CLA, and mass ratio of LD to CLA were 30 degrees C, 1 mL, 12:1, respectively. Thermogravimetric analysis and Fourier transform infrared spectroscopy showed that CLA was successfully encapsulated by LD. The solubility of the LD-CLA complex greatly improved from 62.64 to 91.05% when the temperature was increased from 20 to 90 degrees C. A total of 34.1% CLA of the LD-CLA complex was released into a simulated small intestine environment. Therefore, LD can improve the solubility of the complex and enable the targeted delivery of functional lipids and other bioactive components to the small intestine.
机译:使用由脱支的蜡质玉米淀粉获得的LD作为包囊壁材料,制备线性糊精(LD)-共轭亚油酸(CLA)包合物。目的是通过用水溶性LD封装CLA来制备具有改善的水溶性和在小肠中受控释放的无毒CLA产品。最佳络合温度,用于溶解CLA的乙醇体积以及LD与CLA的质量比分别为30℃,1 mL,12:1。热重分析和傅立叶变换红外光谱表明,CLA被LD成功地包封。当温度从20升高到90摄氏度时,LD-CLA复合物的溶解度从62.64大大提高到91.05%。LD-CLA复合物的总CLA的34.1%被释放到模拟的小肠环境中。因此,LD可以提高复合物的溶解度,并使功能性脂质和其他生物活性成分靶向递送至小肠。

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