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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Effect of Biphasic Calcium Phosphates on Drug Release and Biological and Mechanical Properties of Poly(epsilon-Caprolactone) Composite Membranes
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Effect of Biphasic Calcium Phosphates on Drug Release and Biological and Mechanical Properties of Poly(epsilon-Caprolactone) Composite Membranes

机译:双相磷酸钙对聚(ε-己内酯)复合膜药物释放及生物力学性能的影响

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Poly(epsion-caprolactorte) (PCL) and biphasic calcium phosphate (CaP) composite membranes were prepared for use in tissue regeneration by a novel solvent casting-pressing method. An antibiotic drug, tetracycline hydrochloride (TCH), was entrapped within the membranes to investigate the efficacy of the material as a drug delivery system. The CaP powders were varied in amount (0-50 wt percent) and in powder characteristics by heat treating at different temperatures, and their effects on the mechanical and biological properties and drug release of the membranes were examined. With CaP addition up to 30 wt percent, the elastic modulus of the membranes was enhanced much due to the rigidity of CaP. While the tensile strength and elongation rate decreased gradually with CaP addition because the CaP powders acted as a failure source. The osteoblast-like cells cultured on the CaP-PCL composite membranes exhibited significant improvements in proliferation and alkaline phos-phatase (ALP) activity compared to pure PCL and culture plastic control, indicating excellent cell viability and func-tional activity. The TCH drugs were released from the PCL and CaP-PCL membranes in a similar fashion; an initial burst followed by a reduced release rate. The initial burst effect diminished much by the addition of CaP powders. The CaP addition increased the drug release rate after an initial period, and this was attributed to the high water uptake capacity and dissolution of the CaP containing membranes. Compared to the composite membranes containing heat-treated CaP powders, those with as-precipitated ones had higher dissolution and drug releases. These observations on mechanical properties and cellular responses as well as on drug release profiles suggested that the CaP-PCL composite membranes are potentially applicable to tissue regeneration and drug delivery system.
机译:通过新型溶剂浇铸-压制方法制备了聚己内酯(PCL)和磷酸双相(CaP)复合膜,用于组织再生。抗生素药物四环素盐酸盐(TCH)被截留在膜中,以研究该材料作为药物输送系统的功效。通过在不同温度下进行热处理,CaP粉末的含量(0-50 wt%)和粉末特性会发生变化,并检查了它们对膜的机械和生物学特性以及药物释放的影响。当CaP添加量高达30 wt%时,由于CaP的刚性,膜的弹性模量大大提高。添加CaP会导致拉伸强度和伸长率逐渐降低,因为CaP粉末会成为失效源。与纯PCL和培养塑料对照相比,在CaP-PCL复合膜上培养的成骨样细胞在增殖和碱性磷酸酶(ALP)活性方面表现出显着改善,表明细胞活力和功能极好。 TCH药物以类似的方式从PCL和CaP-PCL膜释放。最初的爆发,然后释放速度降低。通过添加CaP粉末,初始爆裂效果大大降低。 CaP的添加在初始阶段后增加了药物释放速率,这归因于高吸水能力和含CaP膜的溶解。与包含热处理的CaP粉末的复合膜相比,具有沉淀的复合膜具有更高的溶解度和药物释放。这些对机械性能和细胞反应以及药物释放曲线的观察表明,CaP-PCL复合膜可能适用于组织再生和药物输送系统。

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