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纸质出版:2009
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邹志慧,余加林,刘官信,李芳,林丽华,林雅茵.纳米银离子对铜绿假单胞菌生物被膜的细菌死亡率的影响[J].陆军军医大学学报(原第三军医大学学报),2009,31(14):1337-1340.
ZOU Zhi-hui,YU Jia-lin,LIU Guan-xin,LI Fang,LIN Li-hua,LIN Ya-yin.Silver nanoparticles bactericide P. aeruginosa in in vitro biofilm[J].J Amry Med Univ (J Third Mil Med Univ),2009,31(14):1337-1340.
邹志慧,余加林,刘官信,李芳,林丽华,林雅茵.纳米银离子对铜绿假单胞菌生物被膜的细菌死亡率的影响[J].陆军军医大学学报(原第三军医大学学报),2009,31(14):1337-1340. DOI:
ZOU Zhi-hui,YU Jia-lin,LIU Guan-xin,LI Fang,LIN Li-hua,LIN Ya-yin.Silver nanoparticles bactericide P. aeruginosa in in vitro biofilm[J].J Amry Med Univ (J Third Mil Med Univ),2009,31(14):1337-1340. DOI:
目的 探讨纳米银离子对细菌生物被膜(biofilm,BF)的细菌死亡率的影响。 方法 采用摇床法,以纳米银离子含量不同的乙烯-醋酸乙烯酯(Ethylene-Vinyl acetate, EVA)塑料为细菌粘附载体,模拟体内铜绿假单胞菌(P.aeruginosa
PA)BF形成的微环境,建立体外BF模型;将培养3 d的空白标本分别在扫描电子显微镜(SEM)下及用FITC-ConA染色后荧光显微镜下观察不含纳米银离子EVA中BF的形成情况;将生长0.5、1、2、3、5 d的BF模型行SYTO9/PI染色,激光共聚焦扫描电镜(CLSM)下摄取不同层面的图像,然后采用Image Pro Plus 6.0分析软件分析不同干预条件下BF的细菌的死亡率。 结果 运用SEM及荧光显微镜的方法,在以不含纳米银离子EVA塑料的细菌粘附载体上培养3 d的标本中均观察到流线状的BF形成;纳米银离子含量、作用时间对BF的细菌死亡率均有明显影响(F值分别为84.62
85.67,P0.01);不同时间点含有纳米银离子材料的BF细菌死亡率均显著高于空白对照组(P0.05),但纳米银离子含量不同的2种材料上BF的细菌死亡率无明显影响(P0.05);纳米银离子含量不同的(0、0.05%、0.1%)材料上的BF,其第1、2、3天细菌死亡率均分别显著高于第0.5、5天的细菌死亡率(P0.05);含纳米银离子0.1%的材料上BF在作用的第2天其细菌死亡率最高[(88.53±1.88)%]。 结论 运用摇床法成功建立了体外BF模型,纳米银离子对BF内的细菌有明显杀灭作用。
Objective To explore the bactericidal effect of silver nanoparticle on P. aeruginosa in an in vitro model of biofilms. Methods The ethylene-vinyl acetate (EVA) plastics with 0.01% or 0.05% silver nanoparticle in it were used as carriers for the bacteria adhesion
on which bacterial biofilm models in vitro were built by using shaking method to mimic the micro-environment in vivo. The samples not containing silver nanoparticle which had been cultured for 3 d were scanned by scanning electron microscopy (SEM) and were observed by fluorescence microscope after stained with FITC-ConA to observe biofilm formation. The model specimens which had been cultured for 0.5
1
2
3 or 5 d with shaking method were stained by the fluorescent antibody SYTO9/PI
and then detected under confocal laser scanning microscopy (CLSM) to take the images at different levels. The image were were then analyzed by the software of Image-Pro Plus 6.0. The bacterial mortalities under the different conditions (concentration of silver nanoparticles and culture times) were calculated. Results SEM and fluorescence microscope displayed the linear flow of bacterial biofilm formation in the 3-day-cultured EVA plastic carriers
indicating the establishment of in vitro model of biofilm. Mortality of bacteria was obviously affected by the different concentrations of silver ion
duration of action (F=84.62
85.67
P0.0001). The mortality of bacterial of silver nanoparticle was significantly higher than control group at different time points (P0.05). However
there was no significant difference in the mortality between the concentration of 0.05% and 0.1% silver nanoparticle. The mortality of bacteria in the specimens cultured for 1
2 and 3 d was significantly higher than those cultured for 0.5 and 5 d. The mortality rate of bacteria on 0.1% silver nanoparticle EVA plastic cultured for 2 d was the highest among all groups [(88.53±1.88)%]. Conclusion In vitro model of bacterial biofilm is successfully established by using the shaking method. The bacteria in biofilm can be killed by silver nanoparticle.
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