Jixian Zhang , Xinying Lin , Zhiyi Zhang , Jieyu Wang , Ying Wang , Guoyan Liu , Li Liang , Xiaofang Liu , Chaoting Wen , Youdong Li , Xin Xu
{"title":"不同乳化方法制备的核桃油微胶囊:结构、稳定性及释放机理","authors":"Jixian Zhang , Xinying Lin , Zhiyi Zhang , Jieyu Wang , Ying Wang , Guoyan Liu , Li Liang , Xiaofang Liu , Chaoting Wen , Youdong Li , Xin Xu","doi":"10.1016/j.foodhyd.2025.112073","DOIUrl":null,"url":null,"abstract":"<div><div>In the present study, whey protein isolate (WPI), octenyl succinic anhydride (OSA), and resveratrol (Res) were used as wall materials for the preparation of walnut oil microcapsules via the direct mixing method (DM), the layer-by-layer method (LbL), and the Maillard combined mixing method (MCM), respectively. The structural characteristics, release characteristics, and molecular mechanism of microcapsules prepared by different emulsification methods were studied. The results showed that microcapsules prepared by DM (DM-M) exhibit excellent encapsulation performance and oxidation stability compared with microcapsules prepared by LbL (LbL-M) and MCM (MCM-M). The embedding rate of DM-M was 98.88 ± 0.09 %, and the particle size was the smallest (571.33 ± 24.65 nm), showing a smooth and uniform spherical structure. At the end of the intestinal digestion stage, the walnut oil release ratio of DM-M was as high as 80.92 ± 0.86 %, and the free fatty acid release amount was 37.90 ± 2.47 μmol/g, indicating that the shell of DM-M was completely broken down during intestinal digestion. Besides, the order of the interaction forces of DM-M was hydrophobic interaction (S3-S2: 9.99 ± 0.15 mg/mL) > hydrogen bond (S2-S1: 9.89 ± 0.09 mg/mL) > ionic bond (S1: 8.49 ± 0.19 mg/mL) > disulfide bond (S4-S3: 2.60 ± 0.07 mg/mL). The strength of the hydrophobic interaction, hydrogen bond, and ionic bond of LbL-M and MCM-M is weaker than that of DM-M, except for the disulfide bond. DM-M exhibited the strongest non-covalent force of the three microcapsules, which could form a dense structure and effectively prevent walnut oil droplet aggregation. This study provides a theoretical basis for developing high-quality walnut oil microcapsules, extending the shelf life of walnut oil, and embedding fat-soluble active substances.</div></div>","PeriodicalId":320,"journal":{"name":"Food Hydrocolloids","volume":"172 ","pages":"Article 112073"},"PeriodicalIF":11.0000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Walnut oil microcapsules prepared with different emulsification methods: Structure, stability, and release mechanism\",\"authors\":\"Jixian Zhang , Xinying Lin , Zhiyi Zhang , Jieyu Wang , Ying Wang , Guoyan Liu , Li Liang , Xiaofang Liu , Chaoting Wen , Youdong Li , Xin Xu\",\"doi\":\"10.1016/j.foodhyd.2025.112073\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In the present study, whey protein isolate (WPI), octenyl succinic anhydride (OSA), and resveratrol (Res) were used as wall materials for the preparation of walnut oil microcapsules via the direct mixing method (DM), the layer-by-layer method (LbL), and the Maillard combined mixing method (MCM), respectively. The structural characteristics, release characteristics, and molecular mechanism of microcapsules prepared by different emulsification methods were studied. The results showed that microcapsules prepared by DM (DM-M) exhibit excellent encapsulation performance and oxidation stability compared with microcapsules prepared by LbL (LbL-M) and MCM (MCM-M). The embedding rate of DM-M was 98.88 ± 0.09 %, and the particle size was the smallest (571.33 ± 24.65 nm), showing a smooth and uniform spherical structure. At the end of the intestinal digestion stage, the walnut oil release ratio of DM-M was as high as 80.92 ± 0.86 %, and the free fatty acid release amount was 37.90 ± 2.47 μmol/g, indicating that the shell of DM-M was completely broken down during intestinal digestion. Besides, the order of the interaction forces of DM-M was hydrophobic interaction (S3-S2: 9.99 ± 0.15 mg/mL) > hydrogen bond (S2-S1: 9.89 ± 0.09 mg/mL) > ionic bond (S1: 8.49 ± 0.19 mg/mL) > disulfide bond (S4-S3: 2.60 ± 0.07 mg/mL). The strength of the hydrophobic interaction, hydrogen bond, and ionic bond of LbL-M and MCM-M is weaker than that of DM-M, except for the disulfide bond. DM-M exhibited the strongest non-covalent force of the three microcapsules, which could form a dense structure and effectively prevent walnut oil droplet aggregation. This study provides a theoretical basis for developing high-quality walnut oil microcapsules, extending the shelf life of walnut oil, and embedding fat-soluble active substances.</div></div>\",\"PeriodicalId\":320,\"journal\":{\"name\":\"Food Hydrocolloids\",\"volume\":\"172 \",\"pages\":\"Article 112073\"},\"PeriodicalIF\":11.0000,\"publicationDate\":\"2025-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Food Hydrocolloids\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0268005X25010331\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Food Hydrocolloids","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0268005X25010331","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Walnut oil microcapsules prepared with different emulsification methods: Structure, stability, and release mechanism
In the present study, whey protein isolate (WPI), octenyl succinic anhydride (OSA), and resveratrol (Res) were used as wall materials for the preparation of walnut oil microcapsules via the direct mixing method (DM), the layer-by-layer method (LbL), and the Maillard combined mixing method (MCM), respectively. The structural characteristics, release characteristics, and molecular mechanism of microcapsules prepared by different emulsification methods were studied. The results showed that microcapsules prepared by DM (DM-M) exhibit excellent encapsulation performance and oxidation stability compared with microcapsules prepared by LbL (LbL-M) and MCM (MCM-M). The embedding rate of DM-M was 98.88 ± 0.09 %, and the particle size was the smallest (571.33 ± 24.65 nm), showing a smooth and uniform spherical structure. At the end of the intestinal digestion stage, the walnut oil release ratio of DM-M was as high as 80.92 ± 0.86 %, and the free fatty acid release amount was 37.90 ± 2.47 μmol/g, indicating that the shell of DM-M was completely broken down during intestinal digestion. Besides, the order of the interaction forces of DM-M was hydrophobic interaction (S3-S2: 9.99 ± 0.15 mg/mL) > hydrogen bond (S2-S1: 9.89 ± 0.09 mg/mL) > ionic bond (S1: 8.49 ± 0.19 mg/mL) > disulfide bond (S4-S3: 2.60 ± 0.07 mg/mL). The strength of the hydrophobic interaction, hydrogen bond, and ionic bond of LbL-M and MCM-M is weaker than that of DM-M, except for the disulfide bond. DM-M exhibited the strongest non-covalent force of the three microcapsules, which could form a dense structure and effectively prevent walnut oil droplet aggregation. This study provides a theoretical basis for developing high-quality walnut oil microcapsules, extending the shelf life of walnut oil, and embedding fat-soluble active substances.
期刊介绍:
Food Hydrocolloids publishes original and innovative research focused on the characterization, functional properties, and applications of hydrocolloid materials used in food products. These hydrocolloids, defined as polysaccharides and proteins of commercial importance, are added to control aspects such as texture, stability, rheology, and sensory properties. The research's primary emphasis should be on the hydrocolloids themselves, with thorough descriptions of their source, nature, and physicochemical characteristics. Manuscripts are expected to clearly outline specific aims and objectives, include a fundamental discussion of research findings at the molecular level, and address the significance of the results. Studies on hydrocolloids in complex formulations should concentrate on their overall properties and mechanisms of action, while simple formulation development studies may not be considered for publication.
The main areas of interest are:
-Chemical and physicochemical characterisation
Thermal properties including glass transitions and conformational changes-
Rheological properties including viscosity, viscoelastic properties and gelation behaviour-
The influence on organoleptic properties-
Interfacial properties including stabilisation of dispersions, emulsions and foams-
Film forming properties with application to edible films and active packaging-
Encapsulation and controlled release of active compounds-
The influence on health including their role as dietary fibre-
Manipulation of hydrocolloid structure and functionality through chemical, biochemical and physical processes-
New hydrocolloids and hydrocolloid sources of commercial potential.
The Journal also publishes Review articles that provide an overview of the latest developments in topics of specific interest to researchers in this field of activity.