食品科学 ›› 2020, Vol. 41 ›› Issue (7): 14-22.doi: 10.7506/spkx1002-6630-20190307-096

• 基础研究 • 上一篇    下一篇

植物糖原-槲皮素复合物的制备及特征

韦倩倩,樊金玲,朱文学,白喜婷,任国艳   

  1. (河南科技大学食品与生物工程学院,河南 洛阳 471023)
  • 出版日期:2020-04-15 发布日期:2020-04-20
  • 基金资助:
    国家自然科学基金面上项目(31571800);河南省高校科技创新团队支持计划项目(17IRTSTHN016); 河南科技大学实验技术开发基金项目(SY1920001)

Preparation and Characterization of Phytoglycogen-Quercetin Complex

WEI Qianqian, FAN Jinling, ZHU Wenxue, BAI Xiting, REN Guoyan   

  1. (College of Food and Bioengineering, Henan University of Science and Technology, Luoyang 471023, China)
  • Online:2020-04-15 Published:2020-04-20

摘要: 本实验以植物糖原(phytoglycogen,PG)为载体负载槲皮素(quercetin,Qu),制备PG-Qu复合物,研究PG-Qu复合物对Qu的增溶效果,探讨复合物的抗氧化活性以及对癌细胞的抑制作用,并采用动态激光光散射、透射电子显微镜、傅里叶变换红外光谱、X射线衍射对PG-Qu复合物的粒径、形貌、分子相互作用等结构表征进行了分析。结果表明:PG是Qu的高效载体,形成的PG-Qu复合物显著提高了Qu的表观溶解度(P<0.05),负载效果与PG和Qu质量浓度有关,碱性条件有利于PG对Qu的负载,NaCl和醋酸盐的存在不影响复合物的形成。采用5 mg/mL的PG溶液和6 mg/mL的Qu-乙醇溶液在pH 8、不含磷酸盐的条件下负载,制备了PG-Qu复合物溶液,制备的PG-Qu复合物冻干后复溶至PG质量浓度为50 mg/mL时,Qu的表观溶解度为509.46 μg/mL,负载能力为9.68 μg/mg,负载效率为79.88%。与游离Qu相比,PG-Qu复合物的总还原力、羟自由基清除能力以及对癌细胞(MCF-7细胞和A549细胞)增殖的抑制作用均有显著提高;PG和PG-Qu复合物均呈光滑的球形结构,激光粒度仪测定复合物的平均粒径为68~72 nm,且粒度分布均匀;PG负载Qu后Zeta电位由-4.12 mV显著下降至约-10 mV;Qu在PG-Qu复合物中以无定型非晶体的形式存在;氢键是Qu与载体PG发生作用的主要作用力。因此,PG是一种高效的载体,PG-Qu复合物制备简单,可显著提高Qu的表观溶解度、抗氧化活性和癌细胞抑制作用。制备PG-Qu复合物有望成为保障Qu生物学效应、拓宽其在食品工业领域应用的重要途径。

关键词: 植物糖原, 槲皮素, 结构表征, 表观溶解度, 抗氧化活性, 癌细胞抑制能力

Abstract: In this paper, phytoglycogen (PG) was used as a carrier to load quercetin (Qu) to prepare phytoglycogen-quercetin (PG-Qu) complex. The solubility enhancing effect of PG-Qu complex on Qu was studied. The antioxidant activity of PG-Qu complex and its inhibition on cancer cells were investigated. Dynamic laser light scattering, transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) were used to analyze the particle size characteristics, morphology and molecular interaction of the complex. The results showed that PG was a high-efficiency carrier of Qu, and the formed PG-Qu complex significantly improved the apparent solubility of Qu (P < 0.05). The loading efficiency was related to the concentration of PG and Qu. Alkaline condition was beneficial to the loading of PG onto Qu. The presence of NaCl and acetate did not affect the formation of complexes. PG-Qu complex was prepared from 5 mg/mL PG solution and ethanol solution containing 6 mg/mL of Qu at pH 8 without phosphate, which could be lyophilized and reconstituted. When the PG concentration was 50 mg/mL, the solubility of Qu was 509.46 μg/mL, loading capacity 9.68 μg/mg, and loading efficiency 79.88%. Compared with free Qu, the total reducing power, hydroxyl radical scavenging capacity of PG-Qu complex and its inhibitory activity against MCF-7 and A549 cells were significantly improved. Both PG and PG-Qu complex had a smooth spherical structure; the average particle size of the complex was 68–72 nm, and the particle size distribution was uniform. The zeta potential of PG decreased from ?4.12 to ?10 mV after being loaded with Qu. Qu existed in the amorphous form in PG-Qu complex; hydrogen bonding is the main driving force for the interaction between Qu and PG. Therefore, PG is a highly efficient carrier and the preparation of PG-Qu complex is simple, which can significantly improve the apparent solubility, antioxidant activity and anticancer activity of Qu. The preparation of PG-Qu complex is expected to be an important way to maintain the biological effects of Qu and broaden its application in the food industry.

Key words: phytoglycogen (PG), quercetin (Qu), structural characterization, apparent solubility, antioxidant activity, inhibition of cancer cells

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