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具有 pH 响应释放和抗菌活性的碳点修饰的明胶-戊二醛淀粉水凝胶的构建及性能。

Construction and properties of a carbon dots-decorated gelatin-dialdehyde starch hydrogel with pH response release and antibacterial activity.

机构信息

College of Food Science, Northeast Agricultural University, Harbin 150030, China.

College of Food Science, Northeast Agricultural University, Harbin 150030, China.

出版信息

Int J Biol Macromol. 2024 Jan;254(Pt 3):127929. doi: 10.1016/j.ijbiomac.2023.127929. Epub 2023 Nov 14.

DOI:10.1016/j.ijbiomac.2023.127929
PMID:37972844
Abstract

An antibacterial carbon dot hydrogel (GDS) was constructed based on gelatin, dialdehyde starch (DS) and carbon dots (S-PCDs). The formation mechanism of GDS hydrogels was attributed to the synergistic cross-linking of hydrogen bonds and dynamic covalent bonds. With increasing S-PCD content, the mechanical and rheological properties of GDS hydrogels can be improved, and the micropore size becomes denser. GDS hydrogels had pH-dependent swelling and degradation behavior, with a high swelling rate under acidic conditions and relatively low swelling under neutral and alkaline conditions. The cumulative release of S-PCDs from the same hydrogel in an acidic environment was higher than that in an alkaline environment, indicating that the GDS hydrogel had a pH-dependent controlled release ability. The release behavior of S-PCDs conformed to the first-order kinetic release model (R > 0.95), and the release mechanism was related to Fickian diffusion. The synergistic antibacterial mechanism of GDS hydrogels against Staphylococcus aureus suggested that bacterial metabolism leads to an acidic culture environment, which releases S-PCDs and destroys the bacterial cell membrane for antibacterial purposes. In GDS hydrogels, S-PCDs play the main antibacterial role, and the hydrogel plays a synergistic role in trapping bacteria. Carbon dot hydrogels are promising materials to fulfil the functions of antibacterial and controlled release in the food and biomedical fields.

摘要

基于明胶、二醛淀粉(DS)和碳点(S-PCDs)构建了一种抗菌碳点水凝胶(GDS)。GDS 水凝胶的形成机制归因于氢键和动态共价键的协同交联。随着 S-PCD 含量的增加,GDS 水凝胶的力学和流变性能可以得到改善,微孔尺寸变得更加致密。GDS 水凝胶具有 pH 依赖性溶胀和降解行为,在酸性条件下具有较高的溶胀率,而在中性和碱性条件下溶胀率较低。相同水凝胶在酸性环境中的 S-PCDs 累积释放量高于碱性环境,表明 GDS 水凝胶具有 pH 依赖性控制释放能力。S-PCDs 的释放行为符合一级动力学释放模型(R>0.95),释放机制与菲克扩散有关。GDS 水凝胶对金黄色葡萄球菌的协同抗菌机制表明,细菌代谢导致酸性培养环境,从而释放 S-PCDs 并破坏细菌细胞膜以达到抗菌目的。在 GDS 水凝胶中,S-PCDs 发挥主要的抗菌作用,而水凝胶在捕获细菌方面发挥协同作用。碳点水凝胶是满足食品和生物医学领域抗菌和控制释放功能的有前途的材料。

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