纳米纤维经黏膜贴片的研制。

Harleen Grewal, Sanjay R Dhakate, Amit K Goyal, Tanmay S Markandeywar, Basant Malik, Goutam Rath
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引用次数: 19

摘要

在目前的工作中,我们试图利用静电纺聚己内酯(PCL)纳米纤维开发一种新的双氯芬酸钠经黏膜贴片。采用静电纺丝技术制备了不同聚合物浓度的聚氯乙烯纳米纤维。采用扫描电镜(SEM)、红外光谱(FTIR)、载药及Franz扩散池体外释放研究等方法对纳米纤维进行表征。研究表明,13% PCL制备的纳米纤维无断裂、无珠状、超细,直径为120nm。释放研究证实了PCL纳米纤维的缓释行为。纳米纤维可用于非甾体抗炎药的经黏膜给药,提高治疗效果。
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Development of transmucosal patch using nanofibers.

In the present work we have attempted to develop a novel transmucosal patch of diclofenac sodium using electrospun polycaprolactone (PCL) nanofibers. PCL nanofibers were prepared by electrospinning techniques using different polymer concentrations. Nanofibers formulations were characterized by SEM, FTIR, drug loading, and in-vitro release study using Franz diffusion cell. Studies revealed the nanofibers fabricated from 13% PCL were fracture-free, non-beaded, and ultrafine with 120 nm diameter. Release studies demonstrated the sustained release behavior of PCL nanofibers. Nanofibers can be exploited for transmucosal drug delivery of NSAID with improved therapeutic efficacy.

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