{"title":"通过点击化学技术开发细菌纤维素-透明质酸多组分水凝胶,用于生物医学应用","authors":"Şeyma Turan Okulmuş, Burcu Oktay, Dilek Kazan, Nilhan Kayaman Apohan","doi":"10.1134/S0965545X23600564","DOIUrl":null,"url":null,"abstract":"<p>The cross-linking of bacterial cellulose (BC), hydroxypropyl methylcellulose (HPMC), and hyaluronic acid (HA) accomplished with the Copper (I) catalyzed azide-alkyne cycloaddition (CuAAC) click reaction was investigated to obtain the multicomponent hydrogels that allow selective control of material properties. Click chemistry is one of many design methodologies that can be used to create hydrogels for multi-component systems. BC, HPMC, and HA are the most preferred and suitable natural polymers for tissue engineering studies. However, in order to combine their properties in a synergistic way, they must be functionalized to interact with each other. In this study, azide-functional HA was achieved by the reaction of hyaluronic acid with 1-azido-2,3-epoxypropane. To obtain multicomponent hydrogel alkyne-terminated cellulose is also prepared. The cellulose and hyaluronic acid functionalization was confirmed by using FTIR and NMR analysis. The crosslinking reaction took place at ambient conditions for 24 h. It was observed that the swelling capacity of the multi-component hydrogel declined with the increasing amount of BC due to its high crosslinking degree. In addition, the porous morphology of hydrogels makes them suitable for wound dressing applications. SEM results revealed that pore size and porosity decreased with increasing BC concentration. MTT assay demonstrated that the hydrogels promote cell proliferation and adhesion for 3T3 cells. 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SEM results revealed that pore size and porosity decreased with increasing BC concentration. MTT assay demonstrated that the hydrogels promote cell proliferation and adhesion for 3T3 cells. 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引用次数: 0
摘要
摘要 通过铜(I)催化的叠氮-炔环加成(CuAAC)单击反应,研究了细菌纤维素(BC)、羟丙基甲基纤维素(HPMC)和透明质酸(HA)的交联,以获得可选择性控制材料特性的多组分水凝胶。点击化学是可用于制造多组分系统水凝胶的多种设计方法之一。BC、HPMC 和 HA 是组织工程研究中最受欢迎和最合适的天然聚合物。然而,为了以协同增效的方式将它们的特性结合在一起,必须对它们进行官能化处理,使其能够相互影响。在本研究中,通过透明质酸与 1-叠氮-2,3-环氧丙烷的反应实现了叠氮功能化 HA。为了获得多组分水凝胶,还制备了炔端纤维素。傅立叶变换红外光谱和核磁共振分析证实了纤维素和透明质酸的功能化。交联反应在环境条件下进行了 24 小时。观察发现,由于 BC 的交联度较高,多组分水凝胶的溶胀能力随着 BC 用量的增加而下降。此外,水凝胶的多孔形态使其适合用于伤口敷料。扫描电镜结果显示,孔径和孔隙率随着 BC 浓度的增加而减小。MTT 试验表明,水凝胶能促进 3T3 细胞的增殖和粘附。体外细胞培养结果表明,水凝胶具有良好的细胞铺展性。
Development of Bacterial Cellulose-Hyaluronic Acid Multicomponent Hydrogels via Click Chemistry for Biomedical Applications
The cross-linking of bacterial cellulose (BC), hydroxypropyl methylcellulose (HPMC), and hyaluronic acid (HA) accomplished with the Copper (I) catalyzed azide-alkyne cycloaddition (CuAAC) click reaction was investigated to obtain the multicomponent hydrogels that allow selective control of material properties. Click chemistry is one of many design methodologies that can be used to create hydrogels for multi-component systems. BC, HPMC, and HA are the most preferred and suitable natural polymers for tissue engineering studies. However, in order to combine their properties in a synergistic way, they must be functionalized to interact with each other. In this study, azide-functional HA was achieved by the reaction of hyaluronic acid with 1-azido-2,3-epoxypropane. To obtain multicomponent hydrogel alkyne-terminated cellulose is also prepared. The cellulose and hyaluronic acid functionalization was confirmed by using FTIR and NMR analysis. The crosslinking reaction took place at ambient conditions for 24 h. It was observed that the swelling capacity of the multi-component hydrogel declined with the increasing amount of BC due to its high crosslinking degree. In addition, the porous morphology of hydrogels makes them suitable for wound dressing applications. SEM results revealed that pore size and porosity decreased with increasing BC concentration. MTT assay demonstrated that the hydrogels promote cell proliferation and adhesion for 3T3 cells. In vitro cell culturing within the hydrogel demonstrated good cell spreading.
期刊介绍:
Polymer Science, Series A is a journal published in collaboration with the Russian Academy of Sciences. Series A includes experimental and theoretical papers and reviews devoted to physicochemical studies of the structure and properties of polymers (6 issues a year). All journal series present original papers and reviews covering all fundamental aspects of macromolecular science. Contributions should be of marked novelty and interest for a broad readership. Articles may be written in English or Russian regardless of country and nationality of authors. All manuscripts are peer reviewed. Online submission via Internet to the Series A, B, and C is available at http://polymsci.ru.