食品科学 ›› 2024, Vol. 45 ›› Issue (4): 77-87.doi: 10.7506/spkx1002-6630-20230516-154

• 食品化学 • 上一篇    下一篇

姜黄油成分分析及其微乳液的制备、表征、生物活性及体外消化

张佳诺,杨兵,高伟,范丽鹏,桑亚新   

  1. (1.河北农业大学食品科技学院,河北 保定 071000;2.河北省植物资源综合利用重点实验室,晨光生物科技集团股份有限公司,河北 邯郸 057250)
  • 出版日期:2024-02-25 发布日期:2024-03-11
  • 基金资助:
    河北省自然科学基金项目(C2022204211)

Composition of Turmeric Oil and Preparation, Characterization, Bioactivity and in Vitro Digestion of Its Microemulsion

ZHANG Jianuo, YANG Bing, GAO Wei, FAN Lipeng, SANG Yaxin   

  1. (1. College of Food Science and Technology, Hebei Agricultural University, Baoding 071000, China; 2. Key Laboratory of Comprehensive Utilization of Plant Resources in Hebei Province, Chenguang Biotech Group Co. Ltd., Handan 057250, China)
  • Online:2024-02-25 Published:2024-03-11

摘要: 采用气相色谱-质谱联用仪、气相色谱-离子迁移谱联用仪和电子鼻对姜黄油的活性成分进行分析,结果显示相对含量较高组分为芳姜黄酮(23.09%)、姜黄酮(21.36%)和β-姜黄酮(14.93%)。为最大限度提高姜黄油的稳定性以及掩盖其刺激性呈味物质,通过构建微乳液对其进行包封。采用水滴定法制备并以伪三元相图获得姜黄油微乳液的最佳工艺:油相为姜黄油,表面活性剂为吐温80,助表面活性剂为1,2-丙二醇,水相为去离子水,表面活性剂与助表面活性剂的质量比为4∶1,混合表面活性剂与油相的质量比为8∶2,微乳液水分质量分数为70%,此时形成的微乳液区面积最大。对姜黄油微乳液进行表征,测得其pH值为6.81±0.02,密度为(1.053±0.001)g/mL,多分散性指数为0.27±0.11,平均粒径为(32.81±14.54)nm,其为水包油型微乳液,姜黄油微乳液液滴呈球形或椭球形。制备的姜黄油微乳液具有良好的离心稳定性、贮藏稳定性和口腔胃液消化稳定性,可以在肠道中释放并被消化利用。构建微乳液体系可显著提高姜黄油的1,1-二苯基-2-三硝基苯肼自由基和2,2’-联氮双(3-乙基苯并噻唑啉-6-磺酸)阳离子自由基清除率。综上所述,微乳液包封可显著提高姜黄油的稳定性和抗氧化活性,能进入肠道进行有效释放消化,研究结果可为姜黄油高值化开发利用提供理论基础。

关键词: 姜黄油微乳液;伪三元相图;表征;生物活性;体外消化

Abstract: The active components of turmeric oil (TO) were analyzed using gas chromatography-mass spectrometry (GC-MS), gas chromatography-ion mobility spectrometry (GC-IMS), and electronic nose. The major components of TO were found to be ar-curcumone (23.09%), curcumone (21.36%), and β-curcumone (14.93%). In order to maximize the stability of TO and to mask its irritating substances, a microemulsion encapsulating it (TO-ME) was constructed by the water titration method. Based on the pseudo ternary phase diagram constructed, the optimal process parameters were determined as follows: TO as the oil phase, Tween-80 as the surfactant, propylene glycol as the co-surfactant, deionized water as the aqueous phase, a mass ratio of surfactant to co-surfactant of 4:1, a mass ratio of mixed surfactant to oil phase of 8:2, and a water content of 70% in the microemulsion. The largest area of the microemulsion region was formed under these conditions. The resultant microemulsion had a pH of 6.81 ± 0.02, a density of (1.053 ± 0.001) g/mL, a polydispersity index (PDI) of 0.27 ± 0.11, and an average particle size of (32.81 ± 14.54) nm. The microemulsion was characterized as an oil-in-water (O/W) type microemulsion, with spherical or ellipsoidal droplets. The prepared TO-ME exhibited good centrifugal stability, storage stability, and resistance to oral and gastric digestion, and could be released and utilized in the intestine. The microemulsion system significantly improved the scavenging capacity of TO against 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) cation radical. In conclusion, microemulsion encapsulation significantly improved the stability and antioxidant activity of TO while effectively facilitating its release and digestion in the intestine. Our research results provide a theoretical basis for the high-value development and utilization of TO.

Key words: turmeric oil microemulsion; pseudo-ternary phase diagram; characterization; bioactivity; in vitro digestion

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