Characterization of physicochemical properties of mung bean protein isolate and κ-carrageenan hydrogel as a delivery system for propolis extract.

Amin Sabouri Moghadam, Maryam Sadat Mirmohammad Meiguni, Maryam Salami, Gholamreza Askari, Zahra Emam-Djomeh, Mona Miran, Harpal S Buttar, Charles Brennan
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Abstract

A wide range of protein and polysaccharide structures have been applied for the encapsulation of bioactive compounds. In this research, a hydrogel was prepared using mung bean protein isolate and κ-carrageenan as a copolymer. The obtained hydrogel was used for encapsulating propolis at 1 % and 3 % (w/v). The rheological properties and the elasticity of the hydrogel samples with different percentages of propolis was investigated to determine resilience of the hydrogel. The textural analysis illustrated that propolis encapsulation does not change the hydrogel's chewiness, adhesiveness, and hardness. Fluorescence spectroscopy, FTIR, and SDS-PAGE techniques were used to determine the interactions between κ-carrageenan and mung bean protein isolate. The results suggested that electrostatic interactions and covalent bindings are responsible for gel preparation. Hydrophobic interactions contributed to propolis encapsulation. The quenching of aromatic amino acid residue and the clear propolis peak observed in fluorescence spectroscopy represented the role of hydrophobic interactions in encapsulation and gel formation. The water holding capacity (WHC) of >99 % and syneresis of <0.03 % of κ-carrageenan and mung bean protein isolate hydrogel represented an efficient structure of the hydrogel. The peak shifts of κ-carrageenan and mung bean protein isolates illustrated in the FTIR spectra were in line with SDS-PAGE results and fluorescence spectroscopy. The significantly increased encapsulation efficiency of >99 %, release rate of >50 %, and antioxidant activity of propolis encapsulated in κ-carrageenan and mung bean protein isolate suggested that the κ-carrageenan and mung bean protein isolate hydrogel is a potential delivery system and carrier for hydrophobic bioactive compounds, especially propolis.

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绿豆蛋白分离物和κ-卡拉胶水凝胶作为蜂胶提取物输送系统的理化特性表征。
各种蛋白质和多糖结构已被用于封装生物活性化合物。本研究使用绿豆蛋白分离物和κ-卡拉胶作为共聚物制备了一种水凝胶。获得的水凝胶用于封装蜂胶,含量分别为 1 % 和 3 %(重量/体积比)。研究了不同比例蜂胶水凝胶样品的流变特性和弹性,以确定水凝胶的回弹性。纹理分析表明,蜂胶封装不会改变水凝胶的咀嚼性、粘附性和硬度。荧光光谱、傅立叶变换红外光谱和 SDS-PAGE 技术用于确定κ-卡拉胶和绿豆蛋白分离物之间的相互作用。结果表明,静电相互作用和共价结合是凝胶制备的原因。疏水相互作用有助于蜂胶的封装。荧光光谱中观察到的芳香族氨基酸残基淬灭和清晰的蜂胶峰代表了疏水相互作用在封装和凝胶形成中的作用。在κ-卡拉胶和绿豆蛋白分离物中封装的蜂胶的持水量(WHC)大于 99%,滞水量大于 99%,释放率大于 50%,并具有抗氧化活性,这表明κ-卡拉胶和绿豆蛋白分离物水凝胶是一种潜在的疏水性生物活性化合物(尤其是蜂胶)的输送系统和载体。
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