用于引导骨再生的医用级PLA/PEG共聚物自立膜

Ricardo Rojas , Juan P. Zanín , Rocío Martínez , German A. Gil
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引用次数: 0

摘要

可吸收膜和不可吸收膜由于其生物可降解性和生物相容性而被广泛研究作为引导骨再生(GBR)的屏障材料。为了优化其在骨再生中的性能,必须精确设计这些膜的化学、物理和生物特性,平衡机械强度和控制降解。在这项研究中,从医用级PLA/聚乙二醇(PEG)共聚物中开发了用于GBR应用的自立膜。以二氯甲烷为溶剂,羟基磷灰石(HA)和聚乙二醇(PEG)链为添加剂,采用自旋涂覆共聚物油墨制备薄膜。所得薄膜厚度为120 ~ 150 μm,共聚物链排列无序,初始韧性较差。聚乙二醇的掺入增加了薄膜的韧性和亲水性,加速了它们的降解,而透明质酸提高了它们的生物活性,但损害了它们的机械性能。透明质酸和聚乙二醇的结合产生的薄膜在机械完整性和生物活性之间取得了良好的平衡。细胞相容性被证实与MC3T3-E1前成骨细胞,支持这些膜在GBR应用的潜力。在缺乏透明质酸的薄膜中,成骨分化减少,而透明质酸通过作为分化细胞的粘附节点,大大改善了成骨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Self-standing films of medical grade PLA/PEG copolymers for guided bone regeneration
Both resorbable and non-resorbable membranes are intensely investigated as barriers materials for guided bone regeneration (GBR) due to their biodegradability and biocompatibility. To optimize their performance in bone regeneration, the chemical, physical, and biological properties of these membranes must be precisely engineered, balancing mechanical strength and controlled degradation. In this study, self-standing films for GBR applications were developed from medical-grade PLA/polyethylene glycol (PEG) copolymers. The films were prepared by spin coating of copolymer inks that included dichloromethane as a solvent, and hydroxyapatite (HA) and polyethylene glycol (PEG) chains as additives. The resulting films exhibited a thickness of 120–150 μm, a disordered arrangement of the copolymer chains, and initial poor toughness. The incorporation of PEG increased the toughness and hydrophilicity of the films and accelerated their degradation while HA improved their bioactivity but compromised their mechanical properties. The combination of HA and PEG produced films with a favorable balance between mechanical integrity and bioactivity. Cytocompatibility was confirmed with MC3T3-E1 pre-osteoblastic cells, supporting the potential of these films for GBR applications. Osteogenic differentiation was reduced in films lacking HA, whereas HA substantially improved osteogenesis by serving as adhesion nodes for differentiated cells.
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