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通过高强度超声获得的β-乳球蛋白微粒作为生物活性肽浓缩物的潜在递送系统。

β-Lactoglobulin microparticles obtained by high intensity ultrasound as a potential delivery system for bioactive peptide concentrate.

作者信息

Tavares Tânia, Ramos Oscar L, Malcata F Xavier

机构信息

LEPABE - Laboratory of Engineering of Processes, Environment, Biotechnology and Energy, Rua Dr Roberto Frias, 4200-264 Porto, Portugal.

REQUIMTE/Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge Viterbo Ferreira n.º 228, 4050-313 Porto, Portugal.

出版信息

J Food Sci Technol. 2017 Dec;54(13):4387-4396. doi: 10.1007/s13197-017-2912-1. Epub 2017 Oct 12.

Abstract

This work attempted to assess the effect of high intensity ultrasound (HIUS) upon development of bio-based delivery systems, from β-lactoglobulin (β-Lg) gelled microparticles, for encapsulation of a bioactive peptide concentrate (PepC). Solutions of 150 g L of commercial β-Lg and 30 g L PepC, at various pH values (3.0, 4.0 and 5.5), were accordingly subjected to gelation for 30 min using a dry bath kept at 80 °C. The gelled systems were then exposed to HIUS at 0-4 °C, and the effect of processing time (2.5-20.0 min) was ascertained. Laser light scattering and confocal microscopy were used to characterize the particle size distribution, prior to and immediately after HIUS treatment. Gels obtained at pH 5.5 and 4.0 were harder than those obtained at pH 3.0. Ultrasound treatment of gels produced an important reduction in particle mean diameter as sonication time elapsed. Confocal microscopy indicated that application of HIUS led to almost round and monodispersed particles, at both pH 5.5 and 4.0. The peptide encapsulation efficiency was assessed by chromatography and accompanied by assay for bioactivity, after precipitation of the encapsulated material and analysis of the soluble peptides therein.

摘要

本研究旨在评估高强度超声(HIUS)对基于β-乳球蛋白(β-Lg)凝胶化微粒的生物基递送系统开发的影响,该系统用于包封生物活性肽浓缩物(PepC)。将150 g/L商业β-Lg和30 g/L PepC的溶液在不同pH值(3.0、4.0和5.5)下,使用保持在80°C的干浴进行30分钟的凝胶化处理。然后将凝胶化系统在0-4°C下暴露于HIUS,并确定处理时间(2.5-20.0分钟)的影响。在HIUS处理之前和之后,使用激光散射和共聚焦显微镜来表征粒径分布。在pH 5.5和4.0下获得的凝胶比在pH 3.0下获得的凝胶更硬。随着超声处理时间的延长,凝胶的超声处理使颗粒平均直径显著减小。共聚焦显微镜表明,在pH 5.5和4.0下,应用HIUS可产生几乎呈圆形且单分散的颗粒。在包封材料沉淀并分析其中的可溶性肽后,通过色谱法评估肽的包封效率,并同时进行生物活性测定。

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