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Microporous Nano-hydroxyapatite/collagen/phosphatidylserine Scaffolds Embedding Collagen Microparticles for Controlled Drug Delivery in Bone Tissue Engineering

机译:微孔纳米羟基磷灰石/胶原/磷脂酰丝氨酸支架包埋胶原蛋白微粒以控制药物在骨组织工程中的传递

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AbstractScaffolds featuring spatiotemporal control of drug release is highly desirable for bone tissue regeneration. The objective of this study was to construct a scaffold with gradient porosity and drug distribution and evaluate the effect of scaffold structure on drug release kinetics and cell bioactivity. Nano-hydroxyapatite/collagen/phosphatidylserine scaffolds embedded with steroidal saponin loaded collagen microparticles were prepared using a porogen leaching protocol. Morphological characterization showed that the scaffolds consisted of dense layer and loose layer, and pores were interconnective. The microparticles were entrapped at the center of the scaffolds follow a gradient distribution. Release kinetics correlated with the structure. The loose layer showed greater drug release amount as compared to the dense layer. Such differences in release kinetics have distinct effects on cell bioactivity. Cell proliferated much more in loose layer than that in the dense layer. Such spatial and temporal control over drug deposition and delivery within the scaffolds could provide opportunities for tissue regeneration associated with optimum drug doses at wound site, and lessen undesirable drug release and side-effects at uninjured site.
机译:摘要具有时空控制药物释放特性的脚手架是骨骼组织再生的理想之选。本研究的目的是构建具有梯度孔隙率和药物分布的支架,并评估支架结构对药物释放动力学和细胞生物活性的影响。使用致孔剂浸出方案制备了包埋有类固醇皂苷的胶原蛋白微粒的纳米羟基磷灰石/胶原蛋白/磷脂酰丝氨酸支架。形态学表征表明,支架由致密层和疏松层组成,孔相互连通。微粒按照梯度分布截留在支架的中心。释放动力学与结构相关。与致密层相比,疏松层显示出更大的药物释放量。释放动力学的这种差异对细胞生物活性具有明显的影响。细胞在疏松层中的增殖比在致密层中的增殖得多。对支架内药物沉积和递送的这种时空控制可以为伤口部位的最佳药物剂量相关的组织再生提供机会,并减少未受伤部位的不良药物释放和副作用。

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