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负载于含月桂酸和甘油单月桂酸酯的脂质纳米胶囊中的咖啡酸苯乙酯的物理化学表征、释放曲线及抗菌机制

Physicochemical characterization, release profile, and antibacterial mechanisms of caffeic acid phenethyl ester loaded in lipid nanocapsules with lauric acid and glycerol monolaurate.

作者信息

Yang Mengyu, Yan Heng, Zhou Jie, Zhang Junhui, Pan Ya, Zhong Hao, Cai Haiying, Xu Yanqun, Wang Jing, Feng Fengqin, Zhao Minjie

机构信息

College of Biosystems Engineering and Food Science, Zhejiang Key Laboratory for Agro-Food Processing, Zhejiang University, Hangzhou, 310058, China.

College of Food and Pharmacy, Zhejiang Ocean University, Zhoushan, 316022, China.

出版信息

Food Res Int. 2025 May;209:116208. doi: 10.1016/j.foodres.2025.116208. Epub 2025 Mar 21.

Abstract

Numerous studies have demonstrated the biological activities of caffeic acid phenethyl ester (CAPE), including antibacterial, antioxidant, and anti-inflammatory properties. However, the application of CAPE is limited by its low bioavailability and stability. In this work, we designed a CAPE loaded nanocapsule system by using polyoxyl-15-hydroxystearate, coconut oil and lecithin (LE)/lauric acid (LA)/glycerol monolaurate (GML) to improve the release rate of CAPE. The Blank-GML-lipid nanocapsules (BK-GML) and CAPE loaded BK-GML (CAPE-GML) were mainly assembled by hydrophobic forces and electrostatic forces, exhibited a typical spherical shape with a diameter size of less than 90 nm. The encapsulation and loading efficiencies of BK-GML and CAPE-GML reached 74.27 % and 9.61 %, respectively. Lipid nanocapsules (LNCs) also demonstrated a good sustained release of CAPE during in vitro stimulated digestion, indicating LNCs enable sustained CAPE release to the colon. Additionally, they showed a strong antibacterial activity against Escherichia coli and Staphylococcus aureus through the damage of the bacterial cytoderm. Also, BK-GML and CAPE-GML could inhibit the contamination and spread of pathogenic bacteria to be further applied in foods and pharmaceuticals industries.

摘要

大量研究已证明咖啡酸苯乙酯(CAPE)的生物活性,包括抗菌、抗氧化和抗炎特性。然而,CAPE的应用受到其低生物利用度和稳定性的限制。在这项工作中,我们通过使用聚氧乙烯-15-羟基硬脂酸酯、椰子油和卵磷脂(LE)/月桂酸(LA)/甘油单月桂酸酯(GML)设计了一种负载CAPE的纳米胶囊系统,以提高CAPE的释放速率。空白-GML-脂质纳米胶囊(BK-GML)和负载CAPE的BK-GML(CAPE-GML)主要通过疏水力和静电力组装而成,呈现典型的球形,直径尺寸小于90纳米。BK-GML和CAPE-GML的包封率和载药量分别达到74.27%和9.61%。脂质纳米胶囊(LNCs)在体外模拟消化过程中也显示出良好的CAPE缓释效果,表明LNCs能够使CAPE持续释放至结肠。此外,它们通过破坏细菌细胞壁对大肠杆菌和金黄色葡萄球菌表现出强大的抗菌活性。而且,BK-GML和CAPE-GML可以抑制病原菌的污染和传播,有望进一步应用于食品和制药行业。

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