中性粒细胞膜包被纳米颗粒在抗微生物耐药肺炎克雷伯菌感染模型中表现出增强的抗菌活性

IF 4.7 4区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jun Liu MM , Xiaochun Chen BS , Lei Xu MM , Fan Tu BS , Xiaohong Rui BS , Lizhu Zhang MM , Zhihan Yan BS , Yun Liu MM , Renjing Hu BS
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引用次数: 2

摘要

目的探讨中性粒细胞膜包被纳米颗粒介导的KLA肽(KLAKLAKKLAKLAK)和庆大霉素靶向治疗耐药肺炎克雷伯菌(K. pneumonia)肺部感染的疗效和安全性。方法采用动态光散射(DLS)、透射电镜(TEM)、SDS-PAGE、Western blot、定量流式细胞术(QFCM)和共聚焦显微镜对kla -中性粒细胞纳米颗粒(NNPs)进行鉴定。通过小鼠溶血试验、血小板α颗粒膜蛋白浓度、蛋白吸附量、体外巨噬细胞吞噬量、体重变化、肝功能指标、血液生化指标、重要脏器病理变化等评价KLA-NNPs的体外和体内安全性。KLA-NNPs的疗效通过时间杀伤试验、荧光标记试验、细胞内细菌含量、caspase-1活性、存活率和HE染色在体外和体内进行检测。结果制备的KLA-NNPs具有典型的“核壳”结构,纳米尺寸均匀,并将膜蛋白保留在中性粒细胞膜上,达到功能性效果。体外安全性分析表明KLA-NNPs具有良好的血液相容性,在体外可抑制巨噬细胞吞噬。KLA- nnps能有效释放KLA,显著降低胞内细菌和caspase-1活性。体内安全性和有效性分析表明KLA-NNPs具有良好的生物相容性,可有效提高小鼠存活率。结论制备的KLA-NNPs具有良好的纳米医学理化性能和安全性。它可以逃避免疫系统的清除,实现对细菌感染部位的高效靶向聚集和药物递送,有效抑制耐药肺炎克雷伯菌诱导的肺炎的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neutrophil membrane-coated nanoparticles exhibit increased antimicrobial activities in an anti-microbial resistant K. pneumonia infection model

Neutrophil membrane-coated nanoparticles exhibit increased antimicrobial activities in an anti-microbial resistant K. pneumonia infection model

Objective

To investigate the efficacy and safety of neutrophil membrane-coated nanoparticles mediated KLA peptides (KLAKLAKKLAKLAK) and gentamicin in the targeted therapy of anti-microbial resistant Klebsiella pneumoniae (K. pneumonia) lung infection.

Methods

The characteristics of KLA-neutrophils nanoparticles (NNPs) are identified via dynamic light scattering (DLS), transmission electron microscope (TEM), SDS-PAGE, Western blot, quantitative flow cytometry (QFCM) and confocal microscopy. The safety of KLA-NNPs both in vitro and in vivo is evaluated by hemolysis test, platelet α granule membrane protein concentration, protein adsorption capacity, in vitro macrophage phagocytosis, weight change, liver function indicators, blood biochemical indicators, and pathological changes of vital organs in mice. The efficacy of KLA-NNPs is determined by time-kill assay, fluorescent label test, intracellular bacterial content, caspase-1 activity, survival rate, and HE staining both in vitro and in vivo.

Results

The prepared KLA-NNPs have a typical “core-shell” structure, uniform nanometer size, and retain the membrane proteins on the neutrophil membrane that achieve functional effects. In vitro safety analysis showed that KLA-NNPs have good blood compatibility and can inhibit macrophage phagocytosis in vitro. KLA-NNPs can effectively release KLA and significantly reduce intracellular bacteria and caspase-1 activity. In vivo safety analysis and efficacy analysis revealed that KLA-NNPs have good biocompatibility and could effectively improve the survival rate of mice.

Conclusion

The prepared KLA-NNPs have good nano-medicine chemical and physical properties and safety. It can evade immune system clearance, achieve high-efficiency targeted aggregation and drug delivery to bacterial infection sites, and effectively inhibit the development of pneumonia induced by drug-resistant K. pneumonia.

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来源期刊
CiteScore
8.10
自引率
3.60%
发文量
104
审稿时长
4.6 months
期刊介绍: Nanomedicine: Nanotechnology, Biology and Medicine (NBM) is an international, peer-reviewed journal presenting novel, significant, and interdisciplinary theoretical and experimental results related to nanoscience and nanotechnology in the life and health sciences. Content includes basic, translational, and clinical research addressing diagnosis, treatment, monitoring, prediction, and prevention of diseases.
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