Development and characterization of Nile tilapia (Oreochromis niloticus) protein isolate-based biopolymer films incorporated with essential oils and nanoclay

极限抗拉强度 甘油 溶解度 生物高聚物 尼罗罗非鱼 俄勒冈 材料科学 等电点 化学 食品科学 核化学 复合材料 有机化学 生物 渔业 聚合物
作者
Cintia Granzotti da Silva Scudeler,Thayná de Lima Costa,William Renzo Cortez‐Vega,Carlos Prentice,Gustavo Graciano Fonseca
出处
期刊:Food Packaging and Shelf Life [Elsevier BV]
卷期号:25: 100542-100542 被引量:41
标识
DOI:10.1016/j.fpsl.2020.100542
摘要

Fish residues are a natural resource of valuable components, e.g. proteins. The aim of this work was to develop biopolymer films from Nile tilapia (Oreochromis niloticus) protein isolate (NTPI), incorporated with glycerol, montmorillonite nanoclay, and essential oils. The extracted protein was characterized for its isoelectric potential, proximate composition, solubility, water retention capacity (WRC), oil retention capacity (ORC), and color. The casting technique was utilized to obtain the films. Experiments were conducted using a 2(5–1) factorial design with central point. The films were characterized for thickness, solubility in water (Sw), solubility in acid (Sa), water vapor permeability (WVA), and mechanical, structural, and thermal properties. The protein isolate concentered 85 % of the total protein from the raw material. Glycerol, nanoclay, and clove and oregano essential oils were successfully incorporated to the films. The films with the best characteristics were obtained with T6 (1.5 g NTPI, 0.2 g glycerol, 0.4 g oregano essential oil, 0.3 of nanoclay), and T12 (1.5 g NTPI, 0.4 g glycerol, 0.4 g clove essential oil, 0.1 g nanoclay) because they were more stabilized within the cross-linking protein structure. The increase of the protein isolate decreased the Sw of the films but increased the Sa and tensile strength. The Sw ranged from 30.62 to 85.45 %, the Sa between 13.19 and 45.92 %, the WVP between 2.38 and 4.02 g mm/kPa day m2. Tensile strength ranged from 0.65 to 2.76 MPa and elongation from 0.29 to 2.07 %. The essential oils did not show antimicrobial activity when incorporated to the polymer matrix of the films.
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