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基于脲基双子表面活性剂的低分子量水凝胶作为新型可注射生物材料。

Low molecular weight hydrogels derived from urea based-bolaamphiphiles as new injectable biomaterials.

机构信息

Univ. Bordeaux, ARNA Laboratory, F-33016 Bordeaux, France; INSERM U1212, CNRS UMR 5320, ARNA Laboratory, F-33016 Bordeaux, France.

INSERM, U1226, Biotis Laboratory, F-33016 Bordeaux, France.

出版信息

Biomaterials. 2017 Nov;145:72-80. doi: 10.1016/j.biomaterials.2017.08.034. Epub 2017 Aug 19.

DOI:10.1016/j.biomaterials.2017.08.034
PMID:28850933
Abstract

There is a critical need for soft materials in the field of regenerative medicine and tissue engineering. However, designing injectable hydrogel scaffolds encompassing both adequate mechanical and biological properties remains a key challenge for in vivo applications. Here we use a bottom-up approach for synthesizing supramolecular gels to generate novel biomaterial candidates. We evaluated the low molecular weight gels candidates in vivo and identified one urea-containing molecule, compound 16, that avoid foreign body reactions in mice. The self-assembly of bolaamphiphiles creates a unique hydrogel supramolecular structures featuring fast gelation kinetics, high elastic moduli, thixotropic, and thermal reversibility properties. This soft material, which inhibits recognition by macrophages and fibrous deposition, exhibits long-term stability after in vivo injection.

摘要

在再生医学和组织工程领域,软物质材料具有重要的应用价值。然而,设计兼具良好机械性能和生物性能的可注射水凝胶支架仍然是体内应用的一个关键挑战。在这里,我们采用自下而上的方法合成超分子凝胶,以生成新型生物材料候选物。我们对候选的低分子量凝胶进行了体内评估,并鉴定出一种含有尿素的分子,即化合物 16,它可以避免小鼠的异物反应。两亲性 bola 化合物的自组装形成了独特的水凝胶超分子结构,具有快速的凝胶化动力学、高弹性模量、触变性和热可逆性。这种能够抑制巨噬细胞识别和纤维沉积的软物质材料在体内注射后具有长期稳定性。

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