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Preparation and characterization of a novel polylactic acid/hydroxyapatite composite scaffold with biomimetic micro-nanoflbrous porous structure

机译:具有仿生微纳源覆盖多孔结构的新型聚乳酸/羟基磷灰石复合支架的制备与表征

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摘要

Combining synthetic polymer scaffolds with inorganic bioactive factors is widely used to promote the bioactivity and bone conductivity of bone tissue. However, except for the chemical composition of scaffold, the biomimetic structure also plays an important role in its application. In this study, we report the fabrication of polylactic acid/hydroxyapatite (PLA/HA) composite nanofibrous scaffolds via phase separation method to mimic the native extracellular matrix (ECM). The SEM analysis showed that the addition of HA dramatically impacted the morphology of the PLA matrix, which changed from 3D nanofibrous network structure to a disorderly micro-nanofibrous porous structure. At the same time, HA particles could be evenly dispersed at the end of the fiber. The FTIR and XRD demonstrated that there was not any chemical interaction between PLA and HA. Thermal analyses showed that HA could decrease the crystallization of PLA, but improve the thermal decomposition temperature of the composite scaffold. Moreover, water contact angle analysis of the PLA/HA composite scaffold demonstrated that the hydrophilicity increased with the addition of HA. Furthermore, apatite-formation ability tests confirmed that HA could not only more and faster induced the deposition of weak hydroxyapatite but also induced specific morphology of HA.[GRAPHICS].
机译:将合成聚合物支架与无机生物活性因子相结合,广泛用于促进骨组织的生物活性和骨电片。然而,除了支架的化学成分外,仿生结构也在其应用中起重要作用。在这项研究中,我们通过相分离方法报告聚乳酸/羟基磷灰石(PLA / HA)复合纳米纤维支架的制备以模拟天然细胞外基质(ECM)。 SEM分析表明,HA的添加显着影响了PLA矩阵的形态,其从3D纳米纤维网络结构变为无序的微纳米纤维多孔结构。同时,HA颗粒可以均匀地分散在纤维的末端。 FTIR和XRD表明,PLA和HA之间没有任何化学相互作用。热分析表明,HA可以降低PLA的结晶,但是改善了复合支架的热分解温度。此外,PLA / HA复合支架的水接触角分析证明了亲水性随着HA的添加而增加。此外,磷灰石形成能力测试证实,HA不仅越来越快,诱导弱羟基磷灰石的沉积,但也诱导了HA的具体形态。[图形]。

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  • 来源
    《Journal of materials science》 |2020年第8期|74.1-74.11|共11页
  • 作者单位

    Fuzhou Univ Coll Mat Sci & Engn Fuzhou 350108 Peoples R China|Wuyi Univ Coll Ecol & Resource Engn Wuyishan 354300 Peoples R China;

    Fuzhou Univ Coll Mat Sci & Engn Fuzhou 350108 Peoples R China;

    Wuyi Univ Coll Ecol & Resource Engn Wuyishan 354300 Peoples R China;

    Wuyi Univ Coll Ecol & Resource Engn Wuyishan 354300 Peoples R China;

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