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聚乙二醇包覆、载有环丙沙星的氧化铜纳米粒子的绿色合成及其对金黄色葡萄球菌的抗菌活性。

Green synthesis of polyethylene glycol coated, ciprofloxacin loaded CuO nanoparticles and its antibacterial activity against Staphylococcus aureus.

机构信息

Department of Microbiology, The University of Haripur, Haripur, 22620, Pakistan.

Department of Botany, Rawalpindi Women University, Rawalpindi, 4600, Pakistan.

出版信息

Sci Rep. 2024 Sep 11;14(1):21246. doi: 10.1038/s41598-024-72322-1.

Abstract

Antibacterial resistance requires an advanced strategy to increase the efficacy of current therapeutics in addition to the synthesis of new generations of antibiotics. In this study, copper oxide nanoparticles (CuO-NPs) were green synthesized using Moringa oleifera root extract. CuO-NPs fabricated into a form of aspartic acid-ciprofloxacin-polyethylene glycol coated copper oxide-nanotherapeutics (CIP-PEG-CuO) to improve the antibacterial activity of NPs and the efficacy of the drug with controlled cytotoxicity. These NPs were charachterized by Fourier transform infrared spectroscopy (FTIR), x-rays diffraction spectroscopy (XRD), scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS). Antibacterial screening and bacterial chemotaxis investigations demonstrated that CIP-PEG-CuO NPs show enhanced antibacterial potential against Gram-positive and Gram-negative clinically isolated pathogenic bacterial strains as compared to CuO-NPs. In ex-vivo cytotoxicity CIP-PEG-CuO-nano-formulates revealed 88% viability of Baby Hamster Kidney 21 cell lines and 90% RBCs remained intact with nano-formulations during hemolysis assay. An in-vivo studies on animal models show that Staphylococcus aureus were eradicated by this newly developed formulate from the infected skin and showed wound-healing properties. By using specially designed nanoparticles that are engineered to precisely transport antimicrobial agents, these efficient nano-drug delivery systems can target localized infections, ensure targeted delivery, enhance efficacy through increased drug penetration through physical barriers, and reduce systemic side effects for more effective treatment.

摘要

抗菌耐药性需要一种先进的策略,除了合成新一代抗生素之外,还要提高现有治疗方法的疗效。在这项研究中,使用辣木根提取物绿色合成了氧化铜纳米粒子(CuO-NPs)。将 CuO-NPs 制成天冬氨酸-环丙沙星-聚乙二醇包裹的氧化铜纳米治疗剂(CIP-PEG-CuO)的形式,以提高 NPs 的抗菌活性和药物的疗效,并具有控制细胞毒性的作用。这些 NPs 通过傅里叶变换红外光谱(FTIR)、X 射线衍射光谱(XRD)、扫描电子显微镜(SEM)和能谱(EDS)进行了表征。抗菌筛选和细菌趋化性研究表明,与 CuO-NPs 相比,CIP-PEG-CuO NPs 对革兰氏阳性和革兰氏阴性临床分离的致病性细菌菌株表现出增强的抗菌潜力。在体外细胞毒性试验中,CIP-PEG-CuO 纳米制剂显示出 88%的 Baby Hamster Kidney 21 细胞系活力,在溶血试验中 90%的 RBC 保持完整。动物模型的体内研究表明,这种新开发的制剂可以从感染的皮肤中消除金黄色葡萄球菌,并具有伤口愈合特性。通过使用专门设计的纳米粒子,这些纳米粒子被设计成精确地输送抗菌剂,这些高效的纳米药物输送系统可以靶向局部感染,确保靶向输送,通过物理屏障增加药物渗透来提高疗效,并减少全身副作用,从而实现更有效的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3461/11390890/b14079ae241f/41598_2024_72322_Fig1_HTML.jpg

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