Pd/ZIF-8纳米酶介导光热—酶促协同抗菌的研究

The synergistic antibacterial effects of photothermal and enzymatic catalysis mediated by Pd/ZIF-8 nanozyme

  • 摘要:
    目的 探讨Pd/ZIF-8纳米酶介导的光热与酶促协同抗菌性能,评估其在生物医学领域的应用潜力。
    方法 通过水热法制备Pd/ZIF-8纳米酶,并通过透射电子显微镜(TEM)和X射线衍射(XRD)进行结构表征。评估Pd/ZIF-8纳米酶的光热转换性能以及其模拟类过氧化物酶(POD)和谷胱甘肽过氧化物酶(GPx)活性的能力。采用细胞计数试剂盒(CCK-8)检测Pd/ZIF-8对人皮肤成纤维细胞(HDF-a)的毒性情况,同时利用红细胞溶血试验检测其血液相容性。检测在808 nm近红外光照射条件下Pd/ZIF-8对革兰阴性菌(大肠杆菌,E.coli)和革兰阳性菌(耐甲氧西林金黄色葡萄球菌,MRSA)的抗菌性能。
    结果 TEM和XRD分析证实Pd/ZIF-8纳米酶合成成功。Pd/ZIF-8纳米酶具有良好的光热性能,光热转换率达65.3%,且稳定性良好。同时,Pd/ZIF-8纳米酶表现出优异的双重类酶活性(POD和GPx)。细胞毒性及溶血结果表明Pd/ZIF-8具有良好的生物相容性。在近红外光照射下,Pd/ZIF-8对E.coliMRSA的抗菌率分别为97.3% 和99.41%(P<0.000 1)。
    结论 Pd/ZIF-8纳米酶具有介导光热与酶促达到协同抗菌的性能,该纳米材料在抗感染治疗领域展现出良好的应用前景,为开发新型抗菌剂提供了重要思路。

     

    Abstract:
    Objective To explore the synergistic antibacterial performance of photothermal and enzymatic catalysis mediated by Pd/ZIF-8 nanozyme, and assess its potential for biomedical applications.
    Methods The Pd/ZIF-8 nanozyme was prepared by the hydrothermal method, and its structure was characterized by transmission electron microscopy (TEM) and X-ray diffraction (XRD). The photothermal conversion performance of the Pd/ZIF-8 nanozyme and its ability to mimic the activities of peroxidase (POD) and glutathione peroxidase (GPx) were evaluated. The cell counting kit-8 (CCK-8) method was used to detect the toxicity of Pd/ZIF-8 to human dermal fibroblasts (HDF-a), and the erythrocyte hemolysis test was used to detect its blood compatibility. The antibacterial performance of Pd/ZIF-8 against Gram-negative bacteria (Escherichia coli, E. coli) and Gram-positive bacteria (methicillin-resistant Staphylococcus aureus, MRSA) under the irradiation of 808 nm near-infrared light was detected.
    Results TEM and XRD analyses confirmed the successful synthesis of the Pd/ZIF-8 nanozyme. The Pd/ZIF-8 nanozyme exhibited good photothermal performance with a photothermal conversion rate of 65.3% and good stability. Meanwhile, the Pd/ZIF-8 nanozyme exhibited excellent dual enzyme-like activities (POD and GPx). The results of cytotoxicity and hemolysis tests indicated that Pd/ZIF-8 had good biocompatibility. Under near infrared light irradiation, the antibacterial rates of Pd/ZIF-8 against E. coli and MRSA were 97.3% and 99.41%, respectively (P < 0.0001).
    Conclusion The Pd/ZIF-8 nanozyme has the ability to mediate photothermal and enzymatic promotion to achieve synergistic antimicrobial properties. This nanomaterial shows promising application prospects in the field of anti-infection treatment and provides important ideas for the development of new antibacterial agents.

     

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