食品科学 ›› 2026, Vol. 47 ›› Issue (7): 89-100.doi: 10.7506/spkx1002-6630-20250926-216

• 食品化学 • 上一篇    下一篇

湿磨-喷雾制备虾青素微胶囊:载体油对其理化特性、稳定性和生物可及性的影响

陈佳玲,冯裕杰,赵凯欣,肖杰,曹庸,刘晓娟   

  1. (华南农业大学食品学院,广东省功能食品活性物重点实验室,广东 广州 510642)
  • 出版日期:2026-04-15 发布日期:2026-05-08
  • 基金资助:
    广州市重点研发计划项目(SL2022B03J00806);国家自然科学基金面上项目(32172195)

Astaxanthin Microcapsules Prepared by Wet Milling and Spray Drying: Effect of Carrier Oil on Their Physicochemical Properties, Stability, and Bioaccessibility

CHEN Jialing, FENG Yujie, ZHAO Kaixin, XIAO Jie, CAO Yong, LIU Xiaojuan   

  1. (Guangdong Provincial Key Laboratory of Nutraceuticals and Functional Foods, College of Food Science, South China Agricultural University, Guangzhou 510642, China)
  • Online:2026-04-15 Published:2026-05-08

摘要: 通过湿磨-喷雾干燥技术制备无油微胶囊(F1)与含油微胶囊(F2),结合高压均质-喷雾干燥技术制备含赋形剂乳液微胶囊(F3),以物化性质、微观形态、包封效率和表观溶解度为指标,通过加热和储存表征其稳定性,并使用体外模拟消化模型阐明各微胶囊的生物可及性特性。结果表明,F1综合性能最优,虾青素负载量最高(10.12%),水分质量分数较低(3.23%),流动性好,包封率高达98.36%。扫描电镜显示其表面光滑、包覆完整,差示扫描量热、傅里叶变换红外光谱和X射线衍射分析进一步证实其包覆良好。同时,F1的表观溶解度分别是游离虾青素、F2和F3的6.41、2.30、2.32 倍,再水化后粒径最小(420.83 nm),F2次之(441.28 nm),分散稳定性良好。经100 ℃处理,F1及其再分散液中虾青素保留率分别为游离虾青素的1.62、2.04 倍。4 ℃/常温下储存微胶囊210 d后,F1虾青素保留率仍高于81%,是F2和F3的1.04~1.08 倍;储存70 d的再分散液中,F1保留率超85%,F2超80%(均优于F3)。此外,F1的生物可及性是游离虾青素和F3的19.95 倍和1.17 倍,F2的生物可及性是F3的1.30 倍。综上,湿磨-喷雾干燥制备的无载体油虾青素微胶囊在物化特性、稳定性及生物可及性上优势突出,研究结果为其在食品和医药等领域的应用提供了理论基础和技术指导。

关键词: 虾青素;湿磨;微胶囊;载体油;物化特性

Abstract: In this study, oil-free (F1) and direct-contact oil-containing (F2) astaxanthin microcapsules were prepared by wet milling followed by spray drying, and indirect-contact astaxanthin microcapsules (F3) with excipient-emulsified oil were produced by high-pressure homogenization followed by spray drying. The microcapsules were characterized for their physicochemical properties, morphological characteristics, encapsulation efficiency, and apparent solubility. Their stability was evaluated under thermal and long-term storage conditions, and bioaccessibility was determined using an in vitro simulated digestion model. Results demonstrated that among the three types of microcapsules, F1 exhibited the highest astaxanthin payload (10.12%), middle moisture content (3.23%), favorable flowability, and a high encapsulation efficiency of 98.36%. Under scanning electron microscopy (SEM), F1 exhibited smooth and intact surfaces, and differential scanning calorimetry (DSC), Fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD) confirmed the formation of a densely encapsulated structure. The apparent solubility of F1 was 6.41-, 2.30-, and 2.32-fold greater than those of free astaxanthin, F2, and F3, respectively. After rehydration, the particle size of F1 was the smallest (420.83 nm), and F2 was in the middle (441.28 nm), indicating that F1 had the best dispersion stability. After thermal treatment at 100 ℃, F1 and its redispersed solution showed 1.62- and 2.04-fold higher astaxanthin retention than free astaxanthin, respectively. Following 210 days of storage at 4 ℃ or ambient temperature, F1 retained more than 81% of its initial astaxanthin content, 1.04 to 1.08 times that of F2 and F3, respectively. After being stored for 70 days, the redispersed solutions of F1 and F2 showed higher (more than 85% and 80%) astaxanthin retention than that of F3. The bioaccessibility of F1 was 19.95 and 1.17 times those of free astaxanthin and F3, respectively, and the bioaccessibility of F2 was 1.30 times that of F3. In summary, the oil-free astaxanthin microcapsules prepared by wet milling and spray drying offer distinct advantages in terms of physicochemical properties, stability, and bioaccessibility, thereby being promising for applications in functional foods, pharmaceuticals, and related industries.

Key words: astaxanthin; wet grinding; microencapsulation; carrier oil; physicochemical properties

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