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酶交联硫酸化细菌多聚半乳糖醛酸作为 FGF-2 的基于亲和性的载体用于治疗性血管生成。

Enzymatically cross-linkable sulfated bacterial polyglucuronic acid as an affinity-based carrier of FGF-2 for therapeutic angiogenesis.

机构信息

Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-Cho, Toyonaka, Osaka 560-8531, Japan.

Université Clermont Auvergne, Clermont Auvergne INP, CNRS, Institut Pascal, F-63000 Clermont-Ferrand, France; Institut Universitaire de France (IUF), 1 Rue Descartes, 75005 Paris, France.

出版信息

J Biosci Bioeng. 2024 Dec;138(6):541-547. doi: 10.1016/j.jbiosc.2024.08.011. Epub 2024 Sep 28.

Abstract

The fibroblast growth factor-2 (FGF-2) is a critical protein for biological processes such as angiogenesis and tissue regeneration. Recently, hydrogels based on semi-synthetic sulfated polysaccharides have been developed for the controlled delivery of FGF-2. These affinity-based FGF-2 carriers utilizing hydrogels based on sulfated polysaccharides enable sustained delivery of FGF-2, yet choice of materials is limited. Here, we demonstrate a novel synthetic sulfated polysaccharide-based hydrogel based on bacterial polyglucuronic acid (PGU). We synthesized phenol-grafted sulfated PGU (PGUS-Ph), an enzymatically cross-linkable PGU derivative that exhibited an enhanced affinity for FGF-2. The aqueous solution of PGUS-Ph, when combined with FGF-2, could be injected into affected sites and form a hydrogel in a minimally invasive manner. The FGF-2 released from the PGUS-Ph hydrogel induced blood vessel formation, as proven by a chick embryo-based angiogenesis assay. Our results indicate that the PGUS-Ph has the potential as an enzymatically cross-linkable and minimally invasively injectable affinity-based FGF-2 delivery system.

摘要

成纤维细胞生长因子-2(FGF-2)是一种对生物过程至关重要的蛋白质,如血管生成和组织再生。最近,基于半合成硫酸化多糖的水凝胶已被开发用于 FGF-2 的控制释放。这些基于硫酸化多糖的基于亲和力的 FGF-2 载体能够持续释放 FGF-2,但材料的选择有限。在这里,我们展示了一种基于细菌聚葡萄糖醛酸(PGU)的新型合成硫酸化多糖水凝胶。我们合成了酚基接枝硫酸化 PGU(PGUS-Ph),这是一种酶交联的 PGU 衍生物,对 FGF-2 表现出增强的亲和力。PGUS-Ph 的水溶液与 FGF-2 结合后,可以微创方式注入受影响的部位并形成水凝胶。PGUS-Ph 水凝胶释放的 FGF-2 诱导了血管生成,这已通过鸡胚血管生成试验得到证实。我们的结果表明,PGUS-Ph 具有作为酶交联和微创可注射亲和力 FGF-2 递送系统的潜力。

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