石墨烯-生物活性玻璃-P(3HB-co-4HB)复合支架作为伤口愈合前景生物材料的开发与理化评估。

Mohd Aiman Hakimi Abdul Rahim, Siti Fatimah Samsurrijal, Amirul Al-Ashraf Abdullah, Siti Noor Fazliah Mohd Noor
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引用次数: 0

摘要

由于敷料的选择必须优先考虑提供适当的屏障和愈合特性,并考虑患者的顺应性因素,如舒适性、功能性和实用性,因此伤口的临床管理面临着相当大的挑战。本研究的主要目的是开发一种复合支架贴片,以用于伤口愈合。聚(3-羟基丁酸-4-羟基丁酸)[P(3HB-co-4HB)]是一种源自细菌的生物聚合物。由于其独特的机械和物理特性适用于生物医学应用,因此广受认可。石墨烯(G)和生物活性玻璃(BG)对人体具有生物相容性,通过添加生物聚合物可增强其特性。本研究采用溶剂浇注法,将不同比例的 4HB 单体增强的 P(3HB-co-4HB)与 G(3.0 wt.%)和 BG(2.5 wt.%)相结合,开发了两种类型的复合支架:P(3HB-co-25%4HB)/G/BG 和 P(3HB-co-37%4HB)/G/BG。根据对复合材料中有机和无机元素的化学评估,成功研制出了统一结构的复合支架。纯聚合物表面光滑,而添加到复合材料支架中的 BG 和 G 增加了表面粗糙度,形成了不规则的孔隙和突起。就吸水性而言,复合材料的润湿性和亲水性显著提高了 40%。结晶温度的升高降低了复合材料支架的柔韧性。Presto Blue 生物相容性评估表明,复合材料支架调节介质的用量低于 25.00 mg/mL,无毒性。L929 成纤维细胞在两种类型的复合材料支架上都表现出了极佳的粘附性,在 14 天的暴露过程中观察到的细胞存活率增加就是证明。这些研究结果表明,优化复合支架中的每种成分及其相互关系非常重要,可为实现优异的材料特性和提高伤口愈合应用潜力铺平道路。
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Development and physiochemical assessment of graphene-bioactive glass-P(3HB-co-4HB) composite scaffold as prospect biomaterial for wound healing.

The clinical management of wounds presents a considerable challenge because dressing selection must prioritise the provision of appropriate barrier and the healing properties, consider patient's compliance factors such as comfort, functionality and practicality. This study primarily aimed to develop a composite scaffold patch for potential application in wound healing. Poly(3-hydroxybutyrate-co-4-hydroxybutyrate) [P(3HB-co-4HB)] is a biopolymer that originated from bacteria. It is well-recognised owing to its distinctive mechanical and physical characteristics suitable for biomedical applications. Graphene (G) and bioactive glass (BG) are biocompatible towards humans, and enhanced properties are achievable by adding biopolymer. In this study, composite scaffolds were developed by combining P(3HB-co-4HB) at a distinct proportion of 4HB monomer reinforced with G (3.0 wt.%) and BG (2.5 wt.%) by using solvent casting, resulting in two types of composite scaffolds: P(3HB-co-25%4HB)/G/BG and P(3HB-co-37%4HB)/G/BG. A successful composite scaffold as a unified structure was achieved based on chemical assessments of organic and inorganic elements within the composites. The pure polymer displayed a smooth surface, and the BG and G addition into the composite scaffolds increased surface roughness, forming irregular pores and protuberances. The wettability and hydrophilicity of the composites significantly improved up to 40% in terms of water uptake. An increment in crystallisation temperature diminished the flexibility of the composite's scaffolds. Evaluation of Presto Blue biocompatibility demonstrated nontoxic behaviour with a dosage of less than 25.00 mg ml-1of composite scaffold-conditioned media. The L929 fibroblast cells displayed excellent adhesion to both types of composite scaffolds, as evidenced by the increased percentage of cell viability observed throughout 14 d of exposure. These findings demonstrate the importance of optimising each component within the composite scaffolds and their interrelation, paving the way for excellent material properties and enhancing the potential for wound healing applications.

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