食品科学 ›› 2020, Vol. 41 ›› Issue (20): 7-13.doi: 10.7506/spkx1002-6630-20190519-208

• 食品化学 • 上一篇    下一篇

柚皮苷纳米乳液递送体系的消化特性

程喆,潘思轶   

  1. (1.华中农业大学食品科技学院,湖北 武汉 430070;2.华中农业大学环境食品学教育部重点实验室,湖北 武汉 430070)
  • 出版日期:2020-10-25 发布日期:2020-10-23
  • 基金资助:
    国家自然科学基金青年科学基金项目(30901007);湖北省农业科技创新岗位项目(2016620000001044)

Digestion Characteristics of Naringin-Loaded Nanoemulsion Delivery Systems

CHENG Zhe, PAN Siyi   

  1. (1. College of Food Science and Technology, Huazhong Agricultural University, Wuhan 430070, China; 2. Key Laboratory of Environment Correlative Dietology, Ministry of Education, Huazhong Agricultural University, Wuhan 430070, China)
  • Online:2020-10-25 Published:2020-10-23

摘要: 通过体外模拟消化研究以乳清分离蛋白(whey protein isolate,WPI)、ι-卡拉胶(ι-carrageenan,ι-Car)和阿拉伯胶(gum arabic,GA)作为乳化剂稳定的单层以及双层柚皮苷(naringin,NA)纳米乳液的消化规律。对NA单层纳米乳液(NA/WPI-e)和NA双层纳米乳液(NA/WPI/ι-Car-e和NA/WPI/GA-e)进行液滴粒径、Zeta电位和微观结构检测,考察其在胃肠消化阶段的水解程度。结果表明:在胃模拟消化中,单层及双层纳米乳液的液滴聚集,乳液平均粒径显著增大(P<0.05),Zeta电位绝对值基本上高于原始乳液;在小肠模拟消化过程中,NA纳米乳液均发生解絮凝现象。经胃肠消化后NA/WPI-e的游离脂肪酸(free fatty acids,FFAs)释放率最高为97.3%,NA生物利用率为10.06%。NA/WPI/ι-Car-e的FFAs释放率和NA生物利用率均低于NA/WPI-e,而GA质量浓度为1 mg/mL的NA/WPI/GA-e则表现出比NA/WPI-e更高的生物利用率,达到12.13%。NA/WPI-e、NA/WPI/ι-Car-e、NA/WPI/GA-e的FFAs释放率均显著高于对照组(34%),表明纳米乳液递送体系能有效提高NA的生物利用率。

关键词: 体外模拟消化;柚皮苷;纳米乳液;消化特性

Abstract: In this paper, the in vitro digestion patterns of naringin-loaded monolayer and bilayer nanoemulsions constructed by using whey protein isolate (WPI) alone and in combination with ι-carrageenan (ι-Car) or gum arabic (GA) as emulsifiers, named as NA/WPI-e, NA/WPI/ι-Car-e and NA/WPI/GA-e, respectively were studied. The analysis of droplet size, zeta potential and microstructure during simulated gastrointestinal digestion indicated both the single and bilayer nanoemulsions underwent different degrees of hydrolysis. During simulated gastric digestion, the emulsion droplets aggregated, resulting in a significant increase in their average particle size (P < 0.05), and the zeta potential absolute value also increased. During simulated intestinal digestion, deflocculation of the naringin-loaded nanoemulsions was observed. After simulated gastrointestinal digestion, the release rate of free fatty acids (FFAs) and naringin bioavailability of NA/WPI-e were 97.3% and 10.06% respectively. The FFA release rate and naringin bioavailability of NA/WPI/ι-Car-e were lower than those of NA/WPI-e, while NA/WPI/GA-e at 1 mg/mL GA concentration showed the highest naringin bioavailability (12.13%). The FFA release rates of the single and bilayer nanoemulsions were significantly higher than that of the control group (34%), indicating that the nanoemulsion delivery system can effectively improve the bioavailability of naringin.

Key words: in vitro simulated digestion; naringin; nanoemulsion; digestion characteristics

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