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Effect of micropatterning induced surface hydrophobicity on drug release from electrospun cellulose acetate nanofibers

机译:微图案诱导的表面疏水性对静电纺丝醋酸纤维素纳米纤维释放药物的影响

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Sustained release and prevention of burst release for low half-life drugs like Diclofenac sodium is crucial to prevent drug related toxicity. Electrospun nanofibers have emerged recently as potential carrier materials for controlled and sustained drug release. Here, we present a facile method to prevent burst release by tuning the surface wettability through template assisted micropatterning of drug loaded electrospun cellulose acetate (CA) nanofibers. A known amount of drug (Diclofenac sodium) was first mixed with CA and then electrospun in the form of a nanofabric. This as-spun network was hydrophilic in nature. However, when electrospinning was carried out through non-conducting templates, viz nylon meshes with 50 and 100 mu m size openings, two kinds of hydrophobic micro-patterned CA nanofabrics were produced. In vitro transdermal testing of our nanofibrous mats was carried out; these tests were able to show that it would be possible to create a patch for transdermal drug release. Further, our results show that with optimized micro-patterned dimensions, a zero order sustained drug release of up to 12 h may be achieved for the transdermal system when compared to non-patterned samples. This patterning caused a change in the surface wettability, to a hydrophobic surface, resulting in a controlled diffusion of the hydrophilic drug. Patterning assisted in controlling the initial burst release, which is a significant finding especially for low half-life drugs. (C) 2017 Elsevier B.V. All rights reserved.
机译:低半衰期药物(如双氯芬酸钠)的缓释和防止突释对于防止药物相关毒性至关重要。电纺纳米纤维近来已经成为控制和持续释放药物的潜在载体材料。在这里,我们提出了一种简便的方法,可通过负载药物的静电纺丝醋酸纤维素(CA)纳米纤维的模板辅助微图案化来调节表面润湿性,从而防止突发释放。首先将已知量的药物(双氯芬酸钠)与CA混合,然后以纳米织物的形式进行电纺丝。这种初生网络本质上是亲水的。但是,当通过非导电模板(即具有50和100μm尺寸的开口的尼龙网)进行静电纺丝时,会产生两种疏水的微图案CA纳米织物。对我们的纳米纤维垫进行了体外透皮测试;这些测试表明,有可能创建一种用于透皮药物释放的贴剂。此外,我们的结果表明,与无图案的样品相比,通过优化的微图案尺寸,经皮系统可以实现长达12小时的零级持续药物释放。该图案化导致表面向疏水性表面的润湿性改变,从而导致亲水性药物的受控扩散。图案化有助于控制初始突释,这是一个重要发现,尤其是对于低半衰期药物。 (C)2017 Elsevier B.V.保留所有权利。

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