共包封亲水性L-抗坏血酸和疏水性槲皮素的复合凝聚微胶囊化研究
首发时间:2021-02-23
摘要:亲水性和亲脂性活性成分的共包封因其功能协同效应而备受关注。本文选择L-抗坏血酸和槲皮素建立共包封模型,制备了初级W/O乳液,再利用明胶和羧甲基纤维素钠进行复合凝聚,最后通过单宁酸的交联作用进一步稳定抗坏血酸-槲皮素微胶囊。制备的微胶囊平均粒径为69.56 μm,包封效率为65.31%(L-抗坏血酸)和89.61%(槲皮素)。显微形态观察表明,在2%总生物聚合物浓度下,微胶囊为具有多室结构的单核椭圆形,其表面上有一些凹痕和皱缩。X射线衍射光谱表明,L-抗坏血酸和槲皮素的特征衍射峰消失,转变为非结晶结构存在于微胶囊中。热重分析证实双载微胶囊在250 ℃热降解温度下具有良好的热稳定性。共包封的L-抗坏血酸和槲皮素在胃相中都得到了良好的保护,同时在肠相实现了缓释,显着提高了二者的消化稳定性。与游离的L-抗坏血酸和槲皮素相比,其生物利用率均提高了近四倍。
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Co-encapsulation of hydrophilic L-ascorbic acid and hydrophobic quercetin through complex coacervation
Abstract:Co-encapsulation of hydrophilic and hydrophobic nutraceuticals has attracted widespread attention due to its synergistic effect and nutrient collocation. L-ascorbic acid and quercetin were chosen as co-encapsulated models to fabricate a two-step emulsification prior to complex coacervation, including preparation of primary emulsion, gelatin/sodium carboxymethyl cellulose complex coacervation and tannic acid as the cross-linker. The microcapsules had an average particle size of 69.56 μm and the encapsulation efficiency of L-ascorbic acid and quercetin were 65.31% and 89.61%, respectively. Moreover, micro-morphology analysis showed that at 2% total biopolymer concentration, microcapsules exhibited a mononuclear ellipse-like shape with some dents and shrinkages on their surface. X-ray diffraction spectroscopy showed that the co-encapsulated L-ascorbic acid and quercetin were transformed into an amorphous structure in the microcapsules. Also, thermogravimetric analysis indicated better stability at higher thermal degradation temperature. The co-encapsulated L-ascorbic acid and quercetin were both well protected in the gastric phase, while obtaining controlled release in the intestinal phase, significantly improving the stability in vitro release. Compared with free L-ascorbic acid and quercetin, the bioavailability of the encapsulated ones had a fourfold increase.
Keywords: Co-encapsulation Double emulsions Complex coacervation L-ascorbic acid Quercetin
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共包封亲水性L-抗坏血酸和疏水性槲皮素的复合凝聚微胶囊化研究
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