在3月，春暖花開的季節(jié)，讓我們熱烈恭賀中國農(nóng)業(yè)大學(xué)的譚老師成功贏取了恒遠(yuǎn)生物“SCI文獻(xiàn)獎(jiǎng)學(xué)金”！譚老師之前訂購了恒遠(yuǎn)生物高敏ELISA試劑盒，使用了我們的產(chǎn)品在《ADVANCED SCIENCE》雜志上發(fā)表了文獻(xiàn)——Designing Self-Assembling Chimeric Peptide Nanoparticles with High Stability for Combating Piglet Bacterial Infections，IF影響因子高達(dá)16.8分！恒遠(yuǎn)生物在此也非常感謝譚老師對我們信任與支持，希望通過我們的不懈努力能為科研事業(yè)做出更大的貢獻(xiàn)！讓我們再次祝賀譚老師！
Blood was collected from the orbital vein of the mice, ａnd using an enzyme-linked immunoassay to analyze cytokine levels in the serum. The inflammatory factor kit was purchased from Shanghai Hengyuan Biological Technology Co., Ltd.
Moreover, compared with the saline treatment group, the levels of pro-inflammatory factors TNF-α, interleukin-6 (IL-6), ａnd interleukin-1 (IL-1) in the serum of mice in the peptide nanoparticle treatment group were significantly reduced (Figure 6j–l). These cytokines are key factors affecting the inflammatory response in acute sepsis. Considering the action mechanism of peptide nanoparticles, combining them with LPS to reduce the circulation of endotoxins in vivo may limit the immunogenic potential of mice.[41] These results indicate that peptide nanoparticles not only exert direct antibacterial effects but also have immunomodulatory properties. These effects complement each other ａnd help prevent systemic bacterial infections. Hematoxylin ａnd eosin (H&E) staining showed pathological changes in the tissues of infected mice, including hepatocyte damage, vacuoles around the glomerulus, ａnd inflammatory cell infiltration (Figure 6i). After peptide nanoparticle treatment, tissue damage was largely prevented or restored
