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富含余甘子素的提取物包封双乳液:吞噬作用和体外消化过程中生物活性成分的控释

Emblicanin rich extract encapsulated double emulsion: controlled release of bioactive during phagocytosis and in vitro digestion.

作者信息

Chaudhary Neha, Sabikhi Latha, Hussain Shaik Abdul

机构信息

Dairy Technology Division, ICAR-National Dairy Research Institute, Karnal, Haryana 132 001 India.

出版信息

J Food Sci Technol. 2020 Apr;57(4):1371-1381. doi: 10.1007/s13197-019-04171-0. Epub 2019 Nov 16.

Abstract

ABSTRACT

Controlled release of Emblicanin rich water soluble extract of (EEO) from the inner phase of water-in-oil-in-water type double emulsion (DE), during in vitro digestion and phagocytosis was investigated. It was observed that release of EEO (measured as total polyphenols and gallic acid by HPLC) from inner phase of DE was maximum during intestinal digestion followed by gastric and salivary digestion. Main reason was increased particle size of emulsion droplets and change in zeta potential by the action of digestive enzymes. ACE inhibitory activity and antioxidant activity [determined by ABTS (99.58 ± 7.24 mM/mL), DPPH (76.93 ± 0.93 µM/mL) and FRAP (6.34 ± 0.13 mM/mL)] was observed on the higher side in the intestinal digesta of EEO-encapsulated DE (EEODE) as compared to salivary and gastric digesta. However, reverse trend was observed in control sample (unencapsulated-EEO). Phagocytic activity of EEODE increased with increasing its concentration of 2-10 µL. These results indicated that the developed DE matrix was effective in protecting active components of EEO during harsh digestive conditions as evident by sustained/target release. This newly developed EEODE formulation can be used as functional ingredient in the preparation of different dairy and food based functional products.

摘要

摘要

研究了水包油包水型双重乳液(DE)内相中富含余甘子素的水溶性提取物(EEO)在体外消化和吞噬过程中的控释情况。观察到,DE内相中的EEO释放量(通过高效液相色谱法测定总多酚和没食子酸)在肠道消化过程中最大,其次是胃消化和唾液消化。主要原因是消化酶作用使乳液滴粒径增大和zeta电位发生变化。与唾液和胃消化物相比,在EEO包封的DE(EEODE)的肠道消化物中观察到较高的ACE抑制活性和抗氧化活性[通过ABTS(99.58±7.24 mM/mL)、DPPH(76.93±0.93 μM/mL)和FRAP(6.34±0.13 mM/mL)测定]。然而,在对照样品(未包封的EEO)中观察到相反的趋势。EEODE的吞噬活性随其浓度在2 - 10 μL范围内增加而增强。这些结果表明,所开发的DE基质在恶劣的消化条件下能有效保护EEO的活性成分,持续/靶向释放即为明证。这种新开发的EEODE制剂可作为功能性成分用于制备不同的乳制品和食品基功能性产品。

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