首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >Preparation of mussel-inspired injectable hydrogels based on dual-functionalized alginate with improved adhesive, self-healing, and mechanical properties
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Preparation of mussel-inspired injectable hydrogels based on dual-functionalized alginate with improved adhesive, self-healing, and mechanical properties

机译:基于双官能化藻酸盐的贻贝启发注射水凝胶的制备,具有改善的粘合剂,自愈和机械性能

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Injectable hydrogels have aroused much attention for the advantages such as minimally invasive surgery, avoidance of surgical trauma, and filling and repairing irregularly shaped tissue defects. Mussel-inspired injectable hydrogels can be immobilized on the surface of tissues, resulting in stable biomaterial–tissue integration. However, the commonly used biomimetic mussel-inspired hydrogels are prepared by the oxidation of catechol groups, which involves the introduction or production of cytotoxic substances. Moreover, mussel-inspired hydrogels generally display weak mechanical strength and poor adhesiveness because of the consumption of catechol groups during oxidation. Herein, we described a strategy to prepare mussel-inspired injectable hydrogels via the Schiff base reaction. We grafted dopamine, an adhesive motif discovered in the holdfast pads of mussels, to aldehyde-modified alginate backbones. A series of injectable mussel-inspired adhesive, self-healing hydrogels were fabricated by in situ crosslinking of hydrazide-modified poly( L -glutamic acid) (PLGA–ADH) and dual-functionalized alginate (catechol- and aldehyde-modified alginate, ALG–CHO–Catechol). Also, oxidized ALG–CHO–Catechol hydrogels and PLGA/ALG–CHO hydrogels were prepared for comparison. The effects of the crosslinking method, catechol grafting ratio and solid content on the mechanical properties, self-healing behavior, adhesive properties, and hemostatic ability were investigated. Compared with the observations for oxidized ALG–CHO–Catechol hydrogels, more reasonable gelation time and notably enhanced mechanical properties and adhesive behavior were detected in the PLGA/ALG–CHO–Catechol hydrogel system. The PLGA/ALG–CHO–Catechol hydrogels also displayed clear self-healing ability and good cytocompatibility. The strong bioadhesion endowed the PLGA/ALG–CHO–Catechol hydrogels with superior hemostatic performance. These results suggested that PLGA/ALG–CHO–Catechol hydrogel might have great potential as an antibleeding and tissue repair material.
机译:可注射水凝胶引起了很多关注的优势,如微创手术,避免手术创伤,填充和修复不规则形状的组织缺陷。贻贝激发的注射水凝胶可以固定在组织表面上,导致稳定的生物材料 - 组织积分。然而,常用的杀菌贻贝式水凝胶是通过儿茶酚基团的氧化制备的,这涉及细胞毒性物质的引入或产生。此外,由于在氧化过程中消耗儿茶酚基团,贻贝鼓励水凝胶通常显示出弱机械强度和粘合性差。在此,我们描述了一种通过Schiff基础反应制备贻贝启动的注射水凝胶的策略。我们嫁接多巴胺,在贻贝的Holdfast垫中发现的粘合剂图案,到醛改性的藻酸盐骨干。通过酰肼改性聚(L-乙酸)(PLGA-ADH)和双官能化藻酸盐(儿茶酚和醛改性的藻酸盐,ALG,通过原位交联制造一系列可注射贻贝的粘合剂,自愈合水凝胶,通过酰肼交联(PLGA-ADH)和双官能化藻酸盐(儿科和醛改性的藻酸盐,ALG) -cho-catechol)。此外,制备氧化的藻ChO-CateChol水凝胶和PLGA / ALG-CHO水凝胶进行比较。研究了交联方法,儿茶酚接枝比和固体含量对机械性能,自愈合行为,粘合性能和止血能力的影响。与氧化的Alg-Cho-catechol水凝胶的观察结果相比,在PLGA / Alg-Cho-Catechol水凝胶系统中检测到更合理的凝胶化时间和显着提高的机械性能和粘合性能。 PLGA / ALG-CHO-CATECHOL水凝胶还显示出清晰的自我愈合能力和良好的细胞组合。强生的生物粘度赋予PLGA / Alg-Cho-CateChol水凝胶,具有出色的止血性能。这些结果表明,PLGA / Alg-Cho-CateChol Hydrogel可能具有巨大的潜力作为防精和组织修复材料。

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