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The loading and release property of nanoporous anodic alumina for delivery of drugs and drug carriers

机译:纳米多孔阳极氧化铝递送药物和药物携带者的装载和释放性能

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A two-step electrochemical anodisation approach was adopted in this work to create a series of highly ordered mesopores etched with different diameter (60 to 160 nm) and uniform nanotube length in anodised aluminium oxide (AAO). The loading and release characteristics of model drug (indomethacin) and drug carriers (micelles named Pluronic F127, TPGS, PEO-PPO-PEO) were presented to investigate the influence of micelle size, pore diameter and surface modification of AAO on release studies. Surface chemistry was varied via silanation process, using AFTES and PFPTES. It was discovered that quicker release of drugs was induced by larger pore size and smaller micelles. Moreover drug release was found to favour hydrophobic surface as the release was faster in PFPTES modified AAO than the one with APTES.
机译:在这项工作中采用了两步电化学散热方法,以创建一系列高度有序的中孔,其具有不同直径(60至160nm)和阳极氧化铝(AAO)中的均匀纳米管长度。提出了模型药物(吲哚美辛)和药物载体(胶束命名为Pluronic F127,TPG,PEO-PPO-PEO)的装载和释放特性,以研究胶束尺寸,孔径和AAO对释放研究的影响。表面化学通过硅烷工艺改变,使用尾剂和pfptes。有人发现,通过较大的孔径和较小的胶束诱导更快的药物释放。此外,发现药物释放有利于疏水表面,因为释放在pfptes中更快地改性Aao而不是具有脂肪的释放。

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