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Fabrication and characterization of bioactive chitosan microspheres incorporated with mesoporous silica nanoparticles for biomedical applications

机译:结合中孔二氧化硅纳米粒子用于生物医学应用的生物活性壳聚糖微球的制备和表征

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Mesoporous silica nanoparticles (MSNs) were prepared using sol-gel method. Chitosan-MSNs microspheres scaffold loaded with ciprofloxacin also prepared via an ionotropic gelation method. The prepared samples were characterized using FE-SEM, TEM, FTIR and XRD analysis. The pore volume and mean pore diameter for MSNs was determined by the Brunauer-Emmett-Teller (BET) method. The in vitro drug test was evaluated by using UV-Vis spectrophotometry at lambda(max) of 275 nm. The estimated (measured) MSNs pore volume and pore diameter were 0.9227 cm(3)/g and 2.6058 nm, respectively. The Chitosan-MSNs loaded with ciprofloxacin show a spherical surface with good and uniform distribution of the MSNs in the microspheres. The in vitro drug release confirms that the MSNs containing beads shows a retarding release (approximate to 90% in 9 h) than beads without MSNs (approximate to 90% in 2 h). In the light of these findings, the developed delivery system scaffold holds great potential for bone regeneration by control drug release used in activation osteoblast cells.
机译:使用溶胶-凝胶法制备了介孔二氧化硅纳米粒子(MSNs)。载有环丙沙星的壳聚糖-MSNs微球支架也是通过离子凝胶法制备的。使用FE-SEM,TEM,FTIR和XRD分析对制备的样品进行表征。 MSN的孔体积和平均孔径通过Brunauer-Emmett-Teller(BET)方法确定。通过使用紫外可见分光光度法在λ(最大)为275 nm的条件下评估体外药物测试。 MSN的估计(测量)孔径和孔径分别为0.9227 cm(3)/ g和2.6058 nm。载有环丙沙星的壳聚糖-MSNs显示球形表面,MSNs在微球中分布良好且均匀。体外药物释放证实,与不含MSNs的珠子(在2小时内约90%)相比,含MSN的珠子显示出延迟释放(9小时内约90%)。根据这些发现,通过控制用于活化成骨细胞的药物释放,开发的递送系统支架具有巨大的骨再生潜力。

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