纳米纤维
静电纺丝
壳聚糖
抗菌活性
傅里叶变换红外光谱
材料科学
化学工程
扫描电子显微镜
环糊精
聚丙烯腈
聚合物
透射电子显微镜
水溶液
聚电解质
三氯生
高分子化学
作者
Safa Ouerghemmi,Stéphanie Degoutin,Mickaël Maton,Nicolas Tabary,Frédéric Cazaux,Christel Neut,Nicolas Blanchemain,Bernard Martel
出处
期刊:Polymers
[MDPI AG]
日期:2022-05-11
卷期号:14 (10): 1955-1955
被引量:4
标识
DOI:10.3390/polym14101955
摘要
This work focuses on the manufacture of core-sheath nanofibers (NFs) based on chitosan (CHT) as sheath and cyclodextrin polymer (PCD) as core and loaded with triclosan (TCL). In parallel, monolithic NFs consisting of blended CHT-PCD and TCL were prepared. Nanofibers were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Fourier Transform Infrared spectroscopy (FTIR). SEM displayed the morphology of NFs and the structure of the nanowebs, while TEM evidenced the core-sheath structure of NFs prepared by coaxial electrospinning. The core diameters and sheath thicknesses were found dependent on respective flow rates of both precursor solutions. Nanofibers stability and TCL release in aqueous medium were studied and correlated with the antibacterial activity against Staphylococcus aureus and Escherichia coli. Results showed that the release profiles of TCL and therefore the antibacterial activity were directly related to the type of nanofibers. In the case of monolithic nanofibers, the NFs matrix was composed of polyelectrolyte complex (PEC formed between CHT and PCD) and resulted in a prolonged release of TCL and a sustained antibacterial effect. In the case of core-sheath NFs, the PEC was formed only at the core-sheath interface, leading to less stable NFs and therefore to a faster release of TCL, and to a less extended antibacterial activity compared to monolithic ones.
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