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载 LL37 的 ZnO/壳聚糖纳米复合材料作为一种新方法及其对临床分离耐甲氧西林金黄色葡萄球菌生物膜形成抑制作用的评价。

ZnO/chitosan nanocomposites as a new approach for delivery LL37 and evaluation of the inhibitory effects against biofilm-producing Methicillin-resistant Staphylococcus aureus isolated from clinical samples.

机构信息

Department of Microbiology, Faculty of Medicine, Iranshahr University of Medical Sciences, Iranshahr, Iran.

College of Humanities and Sciences, Department of Mathematics, and Science, Ajman University, P.O. Box 346, Ajman, UAE.

出版信息

Int J Biol Macromol. 2023 Dec 31;253(Pt 8):127583. doi: 10.1016/j.ijbiomac.2023.127583. Epub 2023 Oct 20.

Abstract

Modification surface of chitosan nanoparticles using ZnO nanoparticles is important interest in drug delivery because of the beneficial properties. In this study, we proposed a chitosan/ZnO nanocomposite for the targeted delivery of antibacterial peptide (LL37). Synthesized LL37-loaded chitosan/ZnO nanocomposite (CS/ZnO/LL37-NCs) was based on the ionotropic gelation method. The antibacterial activity of the synthesized platform versus Methicillin-resistant Staphylococcus aureus (MRSA) was determined by the microdilution method in 10 mM sodium phosphate buffer. The biofilm formation inhibitory was also evaluated using microtiter plate method. In addition, the ability of CS/ZnO/LL37-NCs on the icaA gene expression level was assessed by the Real-Time PCR. The loading and release investigations confirmed the suitability of CS/ZnO-NCs for LL37 encapsulation. Results showed 6 log CFU/ml reduction in MRSA treated with the CS/ZnO/LL37-NPs. Moreover, CS/ZnO/LL37-NCs showed 81 % biofilm formation inhibition than LL37 alone. Also, icaA gene expression decreased 1-fold in the face of CS/ZnO/LL37-NCs. In conclusion, the modification surface of chitosan nanoparticles with ZnO nanoparticles is a suitable chemical platform for the delivery of LL37 that could be used as a promising nanocarrier for enhancing the delivery of antibacterial peptide and improving the antibacterial activity of LL37.

摘要

壳聚糖纳米粒子表面修饰氧化锌纳米粒子在药物传递中很重要,因为其具有有益的特性。在这项研究中,我们提出了一种壳聚糖/氧化锌纳米复合材料,用于靶向递送抗菌肽(LL37)。合成的负载 LL37 的壳聚糖/氧化锌纳米复合材料(CS/ZnO/LL37-NCs)是基于离子凝胶化方法。通过微量稀释法在 10 mM 磷酸钠缓冲液中测定合成平台对耐甲氧西林金黄色葡萄球菌(MRSA)的抗菌活性。还通过微量滴定板法评估了生物膜形成抑制作用。此外,通过实时 PCR 评估 CS/ZnO/LL37-NCs 对 icaA 基因表达水平的影响。载药和释放研究证实了 CS/ZnO-NCs 适合封装 LL37。结果表明,用 CS/ZnO/LL37-NPs 处理后,MRSA 的减少量为 6 对数 CFU/ml。此外,CS/ZnO/LL37-NCs 比单独的 LL37 表现出 81%的生物膜形成抑制作用。此外,面对 CS/ZnO/LL37-NCs,icaA 基因表达降低了 1 倍。总之,壳聚糖纳米粒子表面修饰氧化锌纳米粒子是一种适合 LL37 传递的化学平台,可作为增强抗菌肽传递和提高 LL37 抗菌活性的有前途的纳米载体。

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