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Electrostatically Self-Assembled Biodegradable Microparticles from Pseudoproteins and Polysaccharide: Fabrication, Characterization, and Biological Properties

机译:伪蛋白质和多糖的静电自组装可生物降解微粒:制备,表征和生物学性质。

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Electrostatically self-assembling hybrid microparticles derived from novel cationic unsaturated arginine-based poly(ester amide) polymers (UArg-PEA) and anionic hyaluronic acid (HA) were fabricated into sub-micron-sized particles in aqueous medium with subsequent UV crosslinking treatment to stabilize the structure. These hybrid microparticles were characterized for size, charge, viscosity, chemical structure, morphology, and biological properties. Depending on the feed ratio of cationic UArg-PEA to anionic HA, the crosslinked microparticles formed spherical structures of 0.772-22.08 mu m in diameter, whereas the uncrosslinked microparticles formed a core with an outer petal-like structure of 2.49-15 mu m in diameter. It was discovered that the morphological structure of the self-assembled microparticles had a profound influence on their biological properties. At a 1:1 feed ratio of UArg-PEA to HA, the uncrosslinked microparticles showed no cytotoxicity toward NIH 3T3 fibroblasts at concentrations up to 20 mu g/mL, and the crosslinked particles exhibited no cytotoxicity at concentrations up to 10 mu g/mL. The UArg-PEA/HA hybrid microparticles exhibited a significantly lower macrophage-induced proinflammatory response (via TNF-alpha) than that from a pure hyaluronic acid control while retaining the beneficial anti-inflammatory IL-10 production by HA. The UArg-PEA/HA microparticles also stimulated size-dependent induction of arginase activity. Therefore, self-assembling these two types of biomaterials in a favorable nontoxic aqueous environment, having complementary biological properties like those of the currently reported UArg-PEA/HA hybrid microparticles, may provide a new class of biomaterials to improve the overall tissue microenvironment for promoting wound healing.
机译:将新型阳离子不饱和精氨酸基聚(酯酰胺)聚合物(UArg-PEA)和阴离子透明质酸(HA)衍生的静电自组装杂化微粒在水性介质中制成亚微米尺寸的颗粒,随后进行UV交联处理稳定结构。这些杂化微粒的尺寸,电荷,粘度,化学结构,形态和生物学特性进行了表征。取决于阳离子UArg-PEA与阴离子HA的进料比,交联的微粒形成直径为0.772-22.08μm的球形结构,而未交联的微粒形成的核芯具有2.49-15μm的外花瓣状结构。直径。已经发现,自组装微粒的形态结构对其生物学特性具有深远的影响。在UArg-PEA与HA的进料比为1:1的情况下,未交联的微粒对浓度高达20μg / mL的NIH 3T3成纤维细胞没有细胞毒性,而交联的微粒对浓度高达10μg / mL的聚乙烯醇没有细胞毒性。 。与纯透明质酸对照相比,UAg-PEA / HA杂合微粒显示出明显更低的巨噬细胞诱导的促炎反应(通过TNF-α),同时保留了HA产生的有益抗炎IL-10。 UArg-PEA / HA微粒还刺激了精氨酸酶活性的大小依赖性诱导。因此,在有利的无毒水性环境中自组装这两种类型的生物材料,具有与目前报道的UArg-PEA / HA杂化微粒相似的互补生物学特性,可能会提供一类新型的生物材料,以改善整体组织的微环境,从而促进伤口愈合。

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