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通过美拉德反应交联的电吹纺葡聚糖/玉米醇溶蛋白纳米纤维的可调物理性质

Tunable Physical Properties of Electro-Blown Spinning Dextran/Zein Nanofibers Cross-Linked by Maillard Reaction.

作者信息

Ren Yupeng, An Jianhui, Tian Cheng, Shang Longchen, Tao Yexing, Deng Lingli

机构信息

College of Biological and Food Engineering, Hubei Minzu University, Enshi 445000, China.

Hubei Key Laboratory of Selenium Resource Research and Biological Application, Hubei Minzu University, Enshi 445000, China.

出版信息

Foods. 2024 Jun 27;13(13):2040. doi: 10.3390/foods13132040.

Abstract

Electrospinning biopolymer nanofibers have emerged as promising candidates for food packaging applications. In this study, dextran/zein nanofibers were fabricated using electro-blown spinning and subsequently cross-linked via the Maillard reaction (MR) at 60 °C and 50% relative humidity. Compared to traditional electrospinning, the introduction of air-blowing improved the sample preparation speed by 10 times. SEM analysis revealed that the nanofiber morphology remained stable upon MR treatment for 24 h. FTIR spectroscopy confirmed that the MR led to a deformation in the protein conformation and an increase in hydrophilicity and elasticity in the nanofibers cross-linked for 6 h. MR treatment for 18 h considerably enhanced the hydrophobicity and elastic modulus owing to covalent bond formation. Thermal analysis indicated an improved thermal stability with increasing MR duration. Mechanical property analysis revealed an increase in elastic modulus and a decrease in elongation at break for the nanofibers cross-linked for more than 6 h, indicating a trade-off between rigidity and flexibility. Notably, the water vapor permeability of the nanofibers cross-linked for 6 and 18 h was remarkably higher, which can be ascribed to the fiber morphology retention upon water evaporation. Overall, MR-cross-linked dextran/zein/xylose nanofibers showed tunable properties, making them a suitable encapsulation system for bioactive compounds.

摘要

静电纺丝生物聚合物纳米纤维已成为食品包装应用中很有前景的候选材料。在本研究中,使用电吹纺丝法制备了葡聚糖/玉米醇溶蛋白纳米纤维,随后在60℃和50%相对湿度下通过美拉德反应(MR)进行交联。与传统静电纺丝相比,引入吹气使样品制备速度提高了10倍。扫描电子显微镜(SEM)分析表明,在美拉德反应处理24小时后,纳米纤维形态保持稳定。傅里叶变换红外光谱(FTIR)证实,美拉德反应导致蛋白质构象变形,交联6小时的纳米纤维亲水性和弹性增加。由于共价键形成,18小时的美拉德反应处理显著提高了疏水性和弹性模量。热分析表明,随着美拉德反应时间的增加,热稳定性得到改善。力学性能分析表明,交联超过6小时的纳米纤维弹性模量增加,断裂伸长率降低,这表明在刚性和柔韧性之间存在权衡。值得注意的是,交联6小时和18小时的纳米纤维的水蒸气透过率显著更高,这可归因于水分蒸发后纤维形态的保留。总体而言,美拉德反应交联的葡聚糖/玉米醇溶蛋白/木糖纳米纤维表现出可调节的性能,使其成为生物活性化合物的合适包封系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b99/11241757/6f5ccd3635ac/foods-13-02040-g001.jpg

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