Department of Microbiology, Faculty of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Institute of Nano Science and Nano Technology, University of Kashan, P.O. Box 87317-51167, Kashan, Iran.
Carbohydr Polym. 2022 Sep 1;291:119634. doi: 10.1016/j.carbpol.2022.119634. Epub 2022 May 19.
In this study, the fabrication of LL37-loaded chitosan nanoparticles (CS/LL37-NPs) was based on an ionotropic gelation method between sodium tripolyphosphate (TPP) and chitosan. Synthesized chitosan nanoparticles (CS-NPs) were approved by Fourier Transform Infrared (FTIR), UV-vis spectroscopy, Dynamic Light Scattering (DLS), Scanning Electron Microscope (SEM), and Transmission Electron Microscopy (TEM). The encapsulation efficiency of LL37 in this delivery system (CS/LL37-NPs) was 86.9%. According to in vitro release profile, the release of LL37 from CS/LL37-NPs was almost complete after 5 days. Additionally, CS/LL37-NPs can cause an increase in the half-life and prolonged LL37 antibacterial activity against Methicillin-resistant Staphylococcus aureus (MRSA). This delivery system demonstrated 68% biofilm formation inhibition compared to the LL37 alone. Also, icaA gene expression in the face of CS/LL37-NPs was significantly decreased. This study showed the important role of delivery systems in enhancing LL37 antibacterial and antibiofilm activity which can be suggested as a promising agent in the inhibition of bacterial growth and the prevention of biofilm formation.
在这项研究中,载 LL37 的壳聚糖纳米粒(CS/LL37-NPs)的制备是基于三聚磷酸钠(TPP)与壳聚糖之间的离子凝胶化方法。合成的壳聚糖纳米粒(CS-NPs)经傅里叶变换红外(FTIR)、紫外可见分光光度法、动态光散射(DLS)、扫描电子显微镜(SEM)和透射电子显微镜(TEM)得到证实。该递药系统(CS/LL37-NPs)中 LL37 的包封效率为 86.9%。根据体外释放曲线,CS/LL37-NPs 中的 LL37 在 5 天后几乎完全释放。此外,CS/LL37-NPs 可使耐甲氧西林金黄色葡萄球菌(MRSA)的半衰期延长,并延长 LL37 的抗菌活性。与单独使用 LL37 相比,该递药系统对生物膜形成的抑制率达到 68%。此外,CS/LL37-NPs 还能显著降低 icaA 基因的表达。本研究表明,递药系统在增强 LL37 的抗菌和抗生物膜活性方面具有重要作用,可作为抑制细菌生长和预防生物膜形成的有前途的药物。