用于封装蜂胶提取物的酪蛋白基纳米载体:设计、制造和表征

JSFA reports Pub Date : 2024-05-31 DOI:10.1002/jsf2.205
Javad Feizy, Mansooreh Soleimanifard, Francesca Maestrelli
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引用次数: 0

摘要

背景 蜂胶因含有天然生物活性化合物而具有多种生物和药理特性。尽管蜂胶具有潜在的健康功效,但由于其香气浓郁、极不稳定、水溶性低和生物利用度低等特点,其在保健食品和药品中的应用非常有限。本研究的目的是制造一种合适、稳定和可生物降解的酪蛋白基纳米载体,作为蜂胶的输送系统。研究人员以不同的蜂胶提取物/酪蛋白比例制备了蜂胶负载酪蛋白纳米载体,并对其理化、结构和热性能进行了评估。 结果 纳米载体的粒径随着蜂胶提取物/酪蛋白比率和酪蛋白浓度的增加而增大。图像处理研究显示,随着纳米载体中蜂胶提取物含量的增加,L*参数(89.743)增加,而b*参数显示黄色减少(14.655)。表面显微照片表明,蜂胶提取物的增加会降低纳米载体的网络紧密度,这与蜂胶提取物/酪蛋白比率越高,载体中蜂胶提取物的包埋量越低有关。X 射线衍射图表明,蜂胶封装会降低酪蛋白的结晶度,而差示扫描量热法和热重/差热分析热图则证明,随着蜂胶提取物含量的增加,纳米载体的热稳定性也会增加。 结论 封装在酪蛋白纳米载体中的蜂胶提取物具有方便的理化特性,可作为生物活性载荷用于食品/医疗系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Casein-based nanocarriers for encapsulation of propolis extract: Design, fabrication, and characterization

Casein-based nanocarriers for encapsulation of propolis extract: Design, fabrication, and characterization

Background

Propolis exhibits multiple biological and pharmacological properties attributed to the presence of natural bio active compounds. In spite of its potential healthy effects, its use in health-food and pharmaceutical products is very restricted due to its intense aroma, highly unstable, low aqueous solubility, and low bioavailability. The purpose of this study is to fabricate an appropriate, stable, and biodegradable casein-based nanocarrier as propolis delivery system. Propolis-loaded casein nanocarriers were prepared at different propolis extract/caseinate ratio and assessed for physicochemical, structural, and thermal properties.

Results

The nanocarriers showed an increase of particle size augmenting propolis extract/caseinate ratio and caseinate concentration. Image processing studies revealed an increase in L* parameter (89.743), while b* parameter revealed a reduction in the yellow color (14.655) increasing the amount propolis extract in the nanocarrier. Surface photomicrographs evidenced that an increment of propolis extract decreased the network compactness of the nanocarriers correlated with the lower entrapment of propolis extract into carriers at higher propolis extract/caseinate ratio. X-ray diffraction pattern suggested that propolis encapsulation produced a decrement in the caseinate crystallinity while differential scanning calorimetry and thermogravimetric/differential thermal analysis thermograms evidenced an increment of thermal stability of nanocarrier with increasing propolis extract content.

Conclusion

Propolis extract encapsulated within casein nanocarriers represented convenient physicochemical attributes and could provide as bioactive load in food/medical system.

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