表皮葡萄球菌
大肠杆菌
抗菌活性
金黄色葡萄球菌
微生物学
生物膜
最小抑制浓度
化学
抗菌剂
细菌
肺炎克雷伯菌
铜绿假单胞菌
肉汤微量稀释
锌
细菌生长
生物
生物化学
有机化学
遗传学
基因
作者
Noppason Pangprasit,Aphisek Kongkaew,Duanghathai Saipinta,Surachai Pikulkaew,Montira Intanon,Witaya Suriyasathaporn,Wasana Chaisri
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2025-02-06
卷期号:17 (2): 209-209
标识
DOI:10.3390/pharmaceutics17020209
摘要
Background/Objectives: This research aimed to determine the efficacy of metallic oxide nanoparticles, especially zinc oxide nanoparticles (ZnO-NPs), in inhibiting a wide range of bacteria isolated from animal wounds, indicating their potential as alternative antimicrobial therapies in veterinary medicine. Method: The disc diffusion technique, broth microdilution technique, and time-kill kinetic assay were performed to determine the antibacterial activity of the ZnO-NPs. Results: Transmission electron microscopy (TEM) and scanning electron microscopy (SEM showed that the ZnO-NPs were spherical and polygonal with sizes ranging from 50 to 100 nm, while DLS (NanoSizer) measured an average size of 512.3 to 535.7 nm with a polydispersity index (PDI) of 0.50 to 0.63 due to particle size agglomeration. The ZnO-NPs exhibited antibacterial activity against several bacterial strains isolated from animal wounds, including Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae, with inhibition zones ranging from 10.0 to 24.5 mm, average MIC values ranging from 1.87 ± 0.36 to 3.12 ± 0.62 mg/mL, and an optimum inhibitory effect against Staphylococcus spp. The time-kill kinetic assay revealed that the Zn-ONPs eradicated Staphylococcus spp. and Klebsiella pneumoniae, as well as Escherichia coli and Pseudomonas aeruginosa (99.9% or 3-log10 reduction), within 30 min of treatment. They also demonstrated a varying degree of antibiofilm formation activity, as indicated by the percentage reduction in biofilm formation compared to the untreated biofilm-forming bacterial strains. Conclusion: ZnO-NPs effectively inhibit bacterial growth and biofilm formation in animal wound isolates.
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