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Encapsulation and controlled release of bioactive compounds in lactoferrin-glycomacropeptide nanohydrogels : curcumin and caffeine as model compounds

机译:乳铁蛋白-糖肽肽纳米水凝胶中生物活性化合物的包封和控制释放:姜黄素和咖啡因为模型化合物

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摘要

Curcumin and caffeine (used as lipophilic and hydrophilic model compounds, respectively) were successfully encapsulated in lactoferrin-glycomacropeptide (Lf-GMP) nanohydrogels by thermal gelation showing high encapsulation efficiencies (>90 %). FTIR spectroscopy confirmed the encapsulation of bioactive compounds in Lf-GMP nanohydrogels and revealed that according to the encapsulated compound different interactions occur with the nanohydrogel matrix. The successful encapsulation of bioactive compounds in Lf-GMP nanohydrogels was also confirmed by fluorescence measurements and confocal laser scanning microscopy. TEM images showed that loaded nanohydrogels maintain their spherical shape with sizes of 112 and 126 nm for curcumin and caffeine encapsulated in Lf-GMP nanohydrogels, respectively; in both cases a polydispersity of 0.2 was obtained.The release mechanisms of bioactive compounds through Lf-GMP nanohydrogels were evaluated at pH 2 and pH 7, by fitting the Linear Superimposition Model to the experimental data. The bioactive compounds release was found to be pH-dependent: at pH 2, relaxation is the governing phenomenon for curcumin and caffeine compounds and at pH 7 Ficks diffusion is the main mechanism of caffeine release while curcumin was not released through Lf-GMP nanohydrogels.
机译:姜黄素和咖啡因(分别用作亲脂性和亲水性模型化合物)通过热凝胶法成功地包裹在乳铁蛋白-糖皮质激素肽(Lf-GMP)纳米水凝胶中,显示出高的包裹效率(> 90%)。 FTIR光谱证实了Lf-GMP纳米水凝胶中生物活性化合物的封装,并揭示了根据封装的化合物与纳米水凝胶基质发生不同的相互作用。通过荧光测量和共聚焦激光扫描显微镜也证实了生物活性化合物在Lf-GMP纳米水凝胶中的成功包封。 TEM图像表明,负载的纳米水凝胶对姜黄素和咖啡因分别封装在Lf-GMP纳米水凝胶中保持其球形,大小分别为112和126 nm。在这两种情况下,均获得了0.2的多分散性。通过将线性叠加模型与实验数据进行拟合,评估了生物活性化合物通过Lf-GMP纳米水凝胶的释放机理。发现生物活性化合物的释放是pH依赖性的:在pH 2时,松弛是姜黄素和咖啡因化合物的主要现象,而在pH 7时,Ficks扩散是咖啡因释放的主要机理,而姜黄素不是通过Lf-GMP纳米水凝胶释放的。

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