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β-乳球蛋白/海藻酸钠复合凝聚体用于黑胡椒(Piper nigrum L.)精油的微胶囊化:模拟胃肠道条件和释放动力学建模。

Complex coacervates of β-lactoglobulin/sodium alginate for the microencapsulation of black pepper (Piper nigrum L.) essential oil: Simulated gastrointestinal conditions and modeling release kinetics.

机构信息

Programa de Pós-graduação em Ciência e Tecnologia de Alimentos (PPGCTA), Universidade Federal Rural do Rio de Janeiro (UFRRJ), Rodovia BR 465, Km 7, 23890-000 Seropédica, RJ, Brazil.

Laboratório de Engenharia e Tecnologia Agroindustrial (LETA), Universidade Federal Fluminense (UFF), Av. dos Trabalhadores, 420, 27255-125 Volta Redonda, RJ, Brazil.

出版信息

Int J Biol Macromol. 2020 Oct 1;160:861-870. doi: 10.1016/j.ijbiomac.2020.05.265. Epub 2020 Jun 1.

DOI:10.1016/j.ijbiomac.2020.05.265
PMID:32497672
Abstract

This study evaluated the most appropriate conditions (pH and biopolymers ratio) for the formation of the complex between β-lactoglobulin (β-lg) and sodium alginate (NaAlg). Furthermore, we microencapsulated black pepper essential oil (EO) using these biopolymers and transglutaminase as a cross-linking agent, and stability during in vitro digestion and its release in food models were studied. A ratio of 17:1 (β-lg/NaAlg) at a pH of 4.5 was the optimal condition for the formation of the complex. The encapsulation efficiency (85.01% ± 0.26) and chemical and morphological characteristics suggested that black pepper EO was microencapsulated using polymers and cross-linking agent naturals. The particle size demonstrated that the capsules produced were on micro scale. The black pepper EO microcapsules lost lower release in water, and the Rigger-Peppas model indicated that the Fickian diffusion mechanism occurred. The microcapsules demonstrated a low release of black pepper EO during oral and gastric digestion and a higher release in intestinal digestion. The black pepper EO after digestion presented high stability (84.8% ± 0.07), and bioaccessibility (31.16% ± 0.3). The results suggest that the black pepper EO was microencapsulated and, preserved in aqueous food model and during oral and gastric conditions tested in vitro.

摘要

本研究评估了β-乳球蛋白(β-lg)与海藻酸钠(NaAlg)形成复合物的最适条件(pH 和生物聚合物比例)。此外,我们使用这些生物聚合物和转谷氨酰胺酶作为交联剂来微封装黑胡椒精油(EO),并研究了其在体外消化过程中的稳定性及其在食品模型中的释放。在 pH 值为 4.5 时,β-lg/NaAlg 比例为 17:1 是形成复合物的最佳条件。包封效率(85.01%±0.26)和化学及形态特征表明,黑胡椒 EO 是使用天然聚合物和交联剂进行微封装的。粒径表明所制备的胶囊处于微尺度。黑胡椒 EO 微胶囊在水中的释放量较低,且 Rigger-Peppas 模型表明发生了菲克扩散机制。微胶囊在口腔和胃消化过程中对黑胡椒 EO 的释放较低,而在肠消化过程中释放较高。消化后的黑胡椒 EO 具有较高的稳定性(84.8%±0.07)和生物利用度(31.16%±0.3)。结果表明,黑胡椒 EO 被微封装,并在水相食品模型以及体外测试的口腔和胃条件下得到保存。

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