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首页> 外文期刊>Biomedical materials >Establishing contact between cell-laden hydrogels and metallic implants with a biomimetic adhesive for cell therapy supported implants
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Establishing contact between cell-laden hydrogels and metallic implants with a biomimetic adhesive for cell therapy supported implants

机译:用仿生粘合剂建立细胞 - 升水水凝胶和金属植入物的接触,用于植入植入物

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For in-dwelling implants, controlling the biological interface is a crucial parameter to promote tissue integration and prevent implant failure. For this purpose, one possibility is to facilitate the establishment of the interface with cell-laden hydrogels fixed to the implant. However, for proper functioning, the stability of the hydrogel on the implant should be ensured. Modification of implant surfaces with an adhesive represents a promising strategy to promote the adhesion of a cell-laden hydrogel on an implant. Herein, we developed a peptidic adhesive based on mussel foot protein (L-DOPA-L-lysine)_2-L-DOPA that can be applied directly on the surface of an implant. At physiological pH, unoxidized (L-DOPA-L-lysine)_2-L-DOPA was supposed to strongly adhere to metallic surfaces but it only formed a very thin coating (less than 1 nm). Once oxidized at physiological pH, (L-DOPA-L-lysine)_2-L-DOPA forms an adhesive coating about 20nmthick. In oxidized conditions, L-lysine can adhere to metallic substrates via electrostatic interaction. Oxidized L-DOPA allows the formation of a coating through self-polymerization and can react with amines so that this adhesive can be used to fix extra-cellular matrix based materials on implant surfaces through the reaction of quinones with amino groups. Hence, a stable interface between a soft gelatin hydrogel and metallic surfaces was achieved and the strength of adhesion was investigated.Wehave shown that the adhesive is non-cytotoxic to encapsulated cells and enabled the adhesion of gelatin soft hydrogels for 21 days on metallic substrates in liquid conditions. The adhesion properties of this anchoring peptide was quantified by a 180° peeling test with a more than 60% increase in peel strength in the presence of the adhesive.Wedemonstrated that by using a biomimetic adhesive, for the application of cell-laden hydrogels to metallic implant surfaces, the hydrogel/implant interface can be ensured without relying on the properties of t
机译:对于内居植入物,控制生物界面是促进组织整合的关键参数,并防止植入物失效。为此,一种可能性是促进与固定到植入物的细胞载体水凝胶的界面建立。然而,为了适当的功能,应确保植入物上的水凝胶的稳定性。用粘合剂改性植入物表面代表了促进细胞升水胶体对植入物的粘附性的有希望的策略。在此,我们开发了基于贻贝泊蛋白(L-DOPA-L-赖氨酸)_2-L-DOPA的肽粘合剂,其可以直接施加在植入物的表面上。在生理pH下,不氧化(L-DOPA-L-赖氨酸)_2-L-DOPA应该强烈地粘附到金属表面上,但它只形成非常薄的涂层(小于1nm)。一旦在生理pH下氧化,(L-DOPA-L-赖氨酸)_2-L-DOPA形成约20nmthick的粘合剂涂层。在氧化条件下,L-赖氨酸可以通过静电相互作用粘附到金属基材上。氧化的L-DOPA允许通过自聚合形成涂层,并可与胺反应,使得通过醌与氨基的反应将该粘合剂固定在植入表面上的细胞基基质基质。因此,实现了柔软明胶水凝胶和金属表面之间的稳定界面,并研究了粘合强度。粘合剂表明,粘合剂是封装细胞的非细胞毒性,使明胶软水凝胶的粘附在金属基材上21天。液体条件。该锚固肽的粘附性能通过180°的剥离试验量化,在粘合剂存在下,剥离强度的增加超过60%。通过使用仿生粘合剂,将细胞 - 载载体水凝胶施用于金属的剥离剂。植入表面,可以确保水凝胶/植入界面而不依赖于T的性质

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