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首页> 外文期刊>Journal of biomaterials science >Release characteristics and processing-structure-performance relationship of electro-spinning curcumin-loaded polyethersulfone based porous ultrafine fibers
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Release characteristics and processing-structure-performance relationship of electro-spinning curcumin-loaded polyethersulfone based porous ultrafine fibers

机译:电纺丝姜黄素负载聚醚砜基多孔超细纤维的释放特性及加工结构 - 性能关系

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摘要

Polymeric porous ultrafine fibers with different structures as drug carrier could be facilely prepared. However, the drug release characteristics and relevant mechanism of different structural porous ultrafine fibers were not well studied. In the present work, different structural Poly-Ether-Sulfone (PES) based porous ultrafine fibers, namely PES, PES/Poly-Ethylene-Glycol (PEG) and PES/Water were prepared by electro-spinning. Curcumin was chosen as drug model loaded in these fibers. Investigation of curcumin release characteristics was carried out by the total immersion in buffer solution. The surface and inner structure of PES based ultrafine fibers were studied by scanning electron microscopy (SEM) in detail. It is found that there is significant difference in the accumulate release amount and release rate with similar structure. About 92.5% of curcumin released within 600min for PES/PEG ultrafine fibers and only 58.9% of curcumin flowed out from PES with 1000min. In order to discuss the fact of this phenomenon, the development structure of PES based porous ultrafine fibers was studied with curcumin release. The results indicated that the curcumin release was directly involved with the structure. For PES/PEG, curcumin around the surface layer released in advance. And then, some penetrable structure emerged with PEG dissolving in the buffer solution, which result in larger specific surface area and more embedded curcumin from the interior structure of the ultrafine fibers diffusing out. For the others, curcumin release only through its own pores of ultrafine fibers. Finally, the processing-structure-performance relationship of PES based porous ultrafine fibers were confirmed by the diversity of porosity and contact angle. The research results demonstrate that PES based porous ultrafine fibers have the potential to be used as drug carrier in the drug delivery according to the practical clinical requirements.
机译:可以易于制备具有不同结构作为药物载体的聚合物多孔超细纤维。然而,不同结构多孔超细纤维的药物释放特性和相关机制尚未得到很好的研究。在本作工作中,通过电动纺丝制备不同结构聚醚 - 砜(PES)的多孔超细纤维,即PE,PE /聚乙二醇(PEG)和PES /水。选择姜黄素作为装载在这些纤维中的药物模型。通过缓冲溶液中的总浸渍进行姜黄素释放特性的研究。通过详细扫描电子显微镜(SEM)研究基于PE的超细纤维的表面和内部结构。发现累积释放量和具有相似结构的释放速率存在显着差异。对于PES / PEG超细纤维,约92.5%的姜黄素释放,仅为58.9%的姜黄素从1000分钟的PE流出。为了讨论这种现象的事实,用姜黄素释放研究了基于PE的多孔超细纤维的显影结构。结果表明,姜黄素释放直接涉及该结构。对于PES / PEG,预先释放的表面层周围的姜黄素。然后,溶解在缓冲溶液中的一些可渗透结构,其导致较大的特定表面积和从漫射的超细纤维的内部结构中的更嵌入的姜黄素。对于其他人来说,姜黄素仅通过其自身的超细纤维毛孔释放。最后,通过孔隙率和接触角的多样性证实了基于PE的多孔超细纤维的加工结构性能关系。研究结果表明,基于PES的多孔超细纤维具有根据实际临床要求在药物递送中用作药物载体的可能性。

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