Heparinized chitosan/hydroxyapatite scaffolds stimulate angiogenesis

Griselda V. Nájera-Romero, Muhammad Yar, Ihtesham Ur Rehman
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引用次数: 9

Abstract

Formation of blood vessels during bone regeneration represents a major challenge for tissue engineered constructs. Poor revascularization can lead to scaffold failure and consequently, leads to non-healing fracture. Heparin is known to bind with angiogenic growth factors influencing the process of new blood vessels formation. There are several problems associated with the use of growth factors in clinic such as low stability, uncontrolled delivery to the site, and high price. The aim of the present study was to explore the potential of heparin to produce pro-angiogenic bone regeneration materials. Chitosan/hydroxyapatite freeze-gelled scaffolds were prepared and loaded with heparin. Different concentrations of heparin were successfully loaded onto the scaffolds, its release from the scaffold was analysed by toluidine blue assay and their angiogenic effect was evaluated by chorioallantoic membrane (CAM) assay to determine the optimal concentration of heparin to induce a proangiogenic effect. It was noted that low heparin concentrations exhibited a positive effect, with approximately 28?μg per scaffold indicating a significant increment in blood vessels. The synthesized materials showed no cytotoxic effects when evaluated by using U2OS cell line.

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肝素化壳聚糖/羟基磷灰石支架刺激血管生成
骨再生过程中血管的形成是组织工程构建的主要挑战。血运重建不良可导致支架失效,从而导致无法愈合的骨折。已知肝素与血管生成生长因子结合,影响新血管形成过程。生长因子在临床应用中存在稳定性低、不可控的给药、价格高等问题。本研究的目的是探索肝素在促血管生成骨再生材料中的潜力。制备了壳聚糖/羟基磷灰石冷冻凝胶支架,并负载肝素。将不同浓度的肝素成功加载到支架上,用甲苯胺蓝法分析其在支架上的释放量,用绒毛尿囊膜(CAM)法评价其血管生成效果,以确定肝素诱导血管生成的最佳浓度。值得注意的是,低肝素浓度表现出积极的作用,约为28?μg /每个支架表明血管显著增加。经U2OS细胞株检测,合成材料无细胞毒作用。
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