Dart Alexander, Sarviya Nandini, Babaie Ali, Clare Jessie, Bhave Mrinal, Sumer Huseyin, de Haan Judy B, Giri Jyotsnendu, Kingshott Peter
Department of Chemistry and Biotechnology, Swinburne University of Technology, Hawthorn, Victoria 3122, Australia.
Department of Chemistry and Biotechnology, Swinburne University of Technology, Hawthorn, Victoria 3122, Australia; Baker Heart and Diabetes Institute, Melbourne, Victoria 3004, Australia.
Biomater Adv. 2023 Nov;154:213641. doi: 10.1016/j.bioadv.2023.213641. Epub 2023 Sep 26.
In this study, a wound dressing of electrospun polycaprolactone (PCL) fibers incorporating the antimicrobial peptide (AMP) nisin was fabricated. Nisin was physically adsorbed to the PCL fibers and tested for antibacterial activity against both Staphylococcus aureus (S. aureus) and Pseudomonas aeruginosa (P. aeruginosa). The PCL fibers had an average diameter of 1.16 μm ± 0.42 μm and no significant change in diameter occurred after nisin adsorption. X-ray photoelectron spectroscopy (XPS) analysis of the fibers detected nitrogen indicative of adsorbed nisin and the signal was used to quantify the levels of coverage on the fiber surfaces. In vitro nisin release studies showed a burst release profile with 80 % of the nisin being released from the fibers within 30 min. Air plasma pre-treatment of the PCL fibers to render them hydrophilic improved nisin loading and release. Antibacterial testing was performed using minimum inhibitory concentration (MIC) and surface attachment assays. The released nisin remained active against both Gram positive S. aureus and Gram negative P. aeruginosa, which has previously been difficult to achieve with single polymer fiber systems. Mammalian cell culture of the nisin coated fibers with L-929 mouse fibroblasts and human epidermal keratinocytes (HEKa) showed that the nisin did not have a significant effect on the biocompatibility of the PCL fibers. The results presented here demonstrate that the physical adsorption, which is a post-treatment, overcomes the potential limitations of harsh chemicals and fabrication conditions of electrospinning from organic solvents and provides a drug loading system having effective antibacterial properties in wound dressings.
在本研究中,制备了一种包含抗菌肽(AMP)乳链菌肽的电纺聚己内酯(PCL)纤维伤口敷料。乳链菌肽被物理吸附到PCL纤维上,并测试了其对金黄色葡萄球菌(S. aureus)和铜绿假单胞菌(P. aeruginosa)的抗菌活性。PCL纤维的平均直径为1.16μm±0.42μm,乳链菌肽吸附后直径无显著变化。对纤维进行X射线光电子能谱(XPS)分析检测到表明乳链菌肽吸附的氮,该信号用于量化纤维表面的覆盖水平。体外乳链菌肽释放研究显示出突发释放曲线,30分钟内80%的乳链菌肽从纤维中释放出来。对PCL纤维进行空气等离子体预处理使其具有亲水性,改善了乳链菌肽的负载和释放。使用最低抑菌浓度(MIC)和表面附着试验进行抗菌测试。释放的乳链菌肽对革兰氏阳性金黄色葡萄球菌和革兰氏阴性铜绿假单胞菌均保持活性,这在以前的单一聚合物纤维系统中很难实现。用L-929小鼠成纤维细胞和人表皮角质形成细胞(HEKa)对涂有乳链菌肽的纤维进行哺乳动物细胞培养表明,乳链菌肽对PCL纤维的生物相容性没有显著影响。此处给出的结果表明,作为后处理的物理吸附克服了有机溶剂静电纺丝中苛刻化学物质和制造条件的潜在限制,并提供了一种在伤口敷料中具有有效抗菌性能的药物负载系统。