食品科学 ›› 2026, Vol. 47 ›› Issue (3): 67-78.doi: 10.7506/spkx1002-6630-20250825-174

• 食品化学 • 上一篇    下一篇

壳聚糖添加量对壳聚糖-籼米淀粉二元基壬酸复合物的影响

关皓天,黄永春,唐湘毅,胡欣月,李子康,王成龙   

  1. (1.广西科技大学生物与化学工程学院,广西 柳州 545005;2.广西糖资源绿色加工重点实验室,广西柳州螺蛳粉技术创新中心,广西 柳州 545005;3.广西职业技术学院食品绿色加工与营养调控研究中心,广西 南宁 530226)
  • 出版日期:2026-02-01 发布日期:2026-03-16
  • 基金资助:
    国家自然科学基金地区科学基金项目(32560587);广西自然科学基金项目(2022JJB160019)

Effect of Chitosan Concentration on Nonanoic Acid-Encapsulated Chitosan-Indica Rice Starch Complex

GUAN Haotian, HUANG Yongchun, TANG Xiangyi, HU Xinyue, LI Zikang, WANG Chenglong   

  1. (1. College of Biological and Chemical Engineering, Guangxi University of Science and Technology, Liuzhou 545005, China; 2. Guangxi Key Laboratory of Green Processing of Suger Resources, Guangxi Liuzhou Luosifen Technology Innovation Center, Liuzhou 545005, China; 3. Research Center for Green Food Processing and Nutritional Regulation, Guangxi Vocational & Technical College, Nanning 530226, China)
  • Online:2026-02-01 Published:2026-03-16

摘要: 为探究壳聚糖-淀粉二元复合物对风味分子壬酸的包埋机制及性能调控规律,本研究系统考察不同分子质量(50、200、500、1 000 kDa)和质量分数(1%、1.5%、2%)的壳聚糖与淀粉形成的复合基质对壬酸包埋能力、包埋稳定性及复合物结构理化特性的影响。对复合凝胶进行质构分析发现,改变壳聚糖分子质量与质量分数可显著调控复合凝胶的质构特性:低至中等分子质量(50、200 kDa)组的硬度、咀嚼性随壳聚糖质量分数升高而降低,500 kDa组则呈上升趋势;流变学特性表明,添加壳聚糖可以增加复合凝胶的储能模量(G′)和损耗模量(G″),糊化温度的调控效果依赖于壳聚糖分子质量与添加量的共同作用,50 kDa壳聚糖以质量分数为1%时延迟糊化效果最优,200、500 kDa壳聚糖则以1.5%添加量效果最佳,1 000 kDa壳聚糖在质量分数为2%时有最佳延迟糊化效果。X射线衍射分析显示,随壳聚糖添加量增加,复合物在7.8°、13°、20°处衍射峰更尖锐;短程有序性分析表明,官能团峰值发生移动但无新特征峰形成,证实分子间作用力发生改变;微观形貌呈现表面光滑、规则的蜂窝状结构;X射线光电子能谱验证了淀粉与壳聚糖的相互作用;热重分析结果表明,1.5%添加量下复合物残余量最大(27.91%,200 kDa组)。本研究可为开发高效风味分子包埋载体及优化食品风味稳定化技术提供理论依据。

关键词: 壳聚糖;淀粉;风味分子;包埋;复合物凝胶

Abstract: To explore the encapsulation mechanism and performance regulatory effect of a chitosan-starch mixture on the flavor molecule nonanoic acid, this study systematically investigated the effects of different molecular masses (50, 200, 500, and 1 000 kDa) and concentrations (1%, 1.5%, and 2%) of chitosan on the encapsulation capacity and stability of nonanoic acid, as well as the structural and physicochemical properties of the resulting complexes. Texture analysis revealed that changing the molecular mass and concentration of chitosan significantly regulated the textural properties of the composite gels: the hardness and chewiness of the low-to-medium molecular weight groups (50 kDa and 200 kDa) decreased with increasing chitosan mass fraction, whereas those of the 500 kDa group showed an upward trend. Rheological properties indicated that the storage modulus (G′) and loss modulus (G″) increased significantly with chitosan addition. The gelatinization temperature was regulated by the joint action of the molecular mass and addition level of chitosan-50, 200, 500, 1 000 kDa chitosan were most effective in delaying starch gelatinization at 1%, 1.5%, 1.5%, and 2% addition levels, respectively. X-ray diffraction (XRD) analysis showed that the diffraction peaks of the complexes at 7.8°, 13°, and 20° became sharper with increasing amount of chitosan. Short-range order analysis indicated that the peak positions of functional groups shifted without the formation of new characteristic peaks, demonstrating changes in intermolecular forces. The morphology presented a regular honeycomb structure with a smooth surface. X-ray photoelectron spectroscopy (XPS) verified the interaction between starch and chitosan. Thermogravimetric analysis (TGA) results showed that the residual amount of the complex with 200 kDa chitosan at 1.5% was the highest (27.91%). This study provides a theoretical basis for the development of efficient carriers for flavor molecules and the optimization of food flavor stabilization technology.

Key words: chitosan; starch; flavor molecules; encapsulation; composite gel

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