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Fabrication and characterization of hydroxyapatite/sodium alginate/ chitosan composite microspheres for drug delivery and bone tissue engineering

机译:羟基磷灰石/藻酸钠/壳聚糖复合微球的制备与表征

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Hydroxyapatite/sodium alginate/chitosan (HA/SA/CS) composite microspheres, which possess good biocompatibility for specific biomedical application, were prepared using an emulsion crosslink technique; calcium ions were used as a cross-linking agent. The effect of the concentration of sodium alginate (SA), the volume ratio of water to oil, the content of hydroxyapatite (HA) nanoparticles, as well as rotation speed, on the morphology and dispersion of composite microspheres were investigated. Also investigated were the drug loading, release behaviors, in vitro hemolysis activity, cytotoxicity, cell adhesion and proliferation capacity of the materials. The results demonstrate that the HA/SA/CS composite microspheres were successfully prepared; their drug loading and encapsulation efficiency are much higher than that of HA nanoparticles. Dox-loaded HA/SA/CS composite microspheres show good pH-sensitive drug-release capability. The hemolysis and cytotoxicity tests suggest that the microspheres have good blood and cell compatibility. Furthermore, the prepared composite microspheres display better cell adhesion and proliferation capacity than HA nanoparticles and HA/SA composite microspheres. Therefore, the HA/SA/CS composite microspheres might have potential as drug carriers in a pH-responsive controlled-release drug delivery system and as candidates for application in bone tissue engineering.
机译:采用乳液交联技术制备了具有良好生物相容性的羟基磷灰石/藻酸钠/壳聚糖(HA / SA / CS)复合微球。钙离子用作交联剂。研究了藻酸钠(SA)的浓度,水与油的体积比,羟基磷灰石(HA)纳米颗粒的含量以及旋转速度对复合微球形态和分散性的影响。还研究了该材料的载药量,释放行为,体外溶血活性,细胞毒性,细胞粘附和增殖能力。结果表明已成功制备了HA / SA / CS复合微球。它们的载药量和包封效率远高于HA纳米颗粒。载有Dox的HA / SA / CS复合微球具有良好的pH敏感药物释放能力。溶血和细胞毒性试验表明,微球具有良好的血液和细胞相容性。此外,与HA纳米颗粒和HA / SA复合微球相比,制备的复合微球显示出更好的细胞粘附和增殖能力。因此,HA / SA / CS复合微球可能具有作为pH响应型控释药物输送系统中的药物载体以及在骨组织工程中应用的候选物。

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