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Synthesis and characterization of flurbiprofen axetil-loaded electrospun MgAl-LDHs/poly(lactic-co-glycolic acid) composite nanofibers

机译:氟比洛芬酯固定电纺丝MgAl-LDHs /聚乳酸-乙醇酸复合纳米纤维的合成与表征

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摘要

We have reported a facile method to fabricate drug-loaded hybrid nanofibers for drug sustained release. In our work, a model drug FA was intercalated into the interlayers of layered double hydroxides (LDHs) by ion-exchange intercalation. The particles were dispersed into the PLGA solution to form the electrospun hybrid nanofibers. The intercalation of FA into the LDHs interlayers (MgAl-FA-LDHs) and the composite nanofibers were characterized via different techniques. The results of XRD and FTIR indicate that FA molecules are intercalated into the MgAl-LDHs interlayers. The formed composite nanofibers exhibit a uniform and smooth morphology and the hydrophilicity did not improve significantly. Importantly, the drug-loaded MgAl-FA-LDHs/PLGA shows a sustained release profile which indicates the MgAl-LDHs can be candidates for drug sustained release.
机译:我们已经报告了一种简便的方法来制造载药的杂化纳米纤维,以实现药物的缓释。在我们的工作中,通过离子交换嵌入将模型药物FA嵌入层状双氢氧化物(LDHs)的中间层。将颗粒分散到PLGA溶液中以形成电纺杂化纳米纤维。通过不同的技术对FA插入LDHs中间层(MgAl-FA-LDHs)和复合纳米纤维中进行了表征。 XRD和FTIR的结果表明,FA分子嵌入MgAl-LDHs中间层。形成的复合纳米纤维表现出均匀且光滑的形态,并且亲水性没有显着改善。重要的是,载有药物的MgAl-FA-LDHs / PLGA显示出持续释放曲线,这表明MgAl-LDHs可以作为药物持续释放的候选药物。

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