柠檬酸盐包覆银纳米颗粒体内外抗鲍曼不动杆菌活性研究

I. G. Auda, I. Salman, Dalal Abed Al-Sattar, Jameelah Ghadban Oduha
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引用次数: 0

摘要

银纳米粒子(AgNPs)由于其有效的抗菌和抗病毒活性而引起潜在的兴趣。封端剂用于表现出比未封端的Ag NP更好的抗菌活性。很少有报道显示AgNPs用于体内抗菌治疗。采用柠檬酸盐还原法制备了柠檬酸盐封端的纳米银;Cit-AgNP的尺寸通过原子力显微镜(AFM)测定,并且在15-90nm之间。鲍曼不动杆菌分离株是唯一对CitAgNP敏感的菌种。Cit-AgNPs的MIC和MBC是用鲍曼菌测定的。结果显示了Cit-AgNPs的添加效应。四组小鼠经腹膜内注射亚致死剂量的鲍曼不动杆菌(IP)。Cit-AgNPs和亚胺培南加Cit-AgNP组合的单日剂量给予IP。亚胺培南和磷酸盐缓冲盐水(PBS)分别作为阳性对照和阴性对照。有趣的是,只有PBS处理组在牺牲小鼠的肝脏和脾脏中显示出鲍曼不动杆菌的生长。在组织病理学上,Cit-AgNPs在体内外与亚胺培南联合使用时表现出抗菌活性并具有相加作用。此外,Cit-AgNPs显示出剂量依赖性活性,即使在高剂量给药后,器官对Cit-AgNP毒性作用的照射也不同。总之,Cit封端的AgNPs对多重耐药(MDR)鲍曼菌具有抗菌活性,但对肺炎克雷伯菌和大肠杆菌没有抗菌活性。Cit封端的AgNPs以加性效应增加了亚胺培南的抑制区;Citpapped AgNPs的最小抑制浓度和最小杀菌浓度相对较低。当单独或与亚胺培南联合给药时,Cit封端的AgNPs在体内消除了鲍曼不动杆菌感染。Cit-AgNPs的细胞毒性是剂量依赖性的,并且在高剂量给药后,器官对Cit-AgNP炎症作用的照射不同。不建议系统使用Cit封端的AgNPs,尽管它们具有宝贵的附加抗菌作用,特别是在高剂量和与亚胺培南联合使用时,需要评估局部给药。
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In-vivo and In-vitro Anti-Acinetobacter baumannii Activity of Citrate-Capped Silver Nanoparticles
Silver nanoparticles (AgNPs) are of potential interest because of their effective antibacterial and antiviral activities. Capping agents are used for exhibiting a better antibacterial activity than uncapped Ag NPs. There are very few reports that have shown the usage of AgNPs for in-vivo antibacterial therapy. Citrate-capped silver nanoparticles were synthesized chemically by citrate reduction method; the size of Cit-AgNPs was determined by an atomic force microscope (AFM) and was between 15 90 nm. Acinetobacter baumannii (A. baumannii) isolates were the only sensitive species to CitAgNPs. MICs and MBC of Cit-AgNPs were determined by using A. baumannii. The results showed an additive effect of Cit-AgNPs. Four mice groups were infected with a sub-lethal dose of A. baumannii intraperitoneally, IP. The single daily dose of Cit-AgNPs and imipenem plus Cit-AgNPs combination were administered IP. Imipenem and phosphate buffer saline (PBS) was used as positive control and negative control, respectively. Interestingly, only the PBS-treated group showed growth of A. baumannii in the liver and spleen of sacrificed mice. Histopathologically, Cit-AgNPs showed antibacterial activity and had an additive effect when combined with imipenem in vivo and in vitro. Moreover, the Cit-AgNPs showed dose-dependent activity and the organs differed in the illumination of the toxicity effect of Cit-AgNPs even after high dose administration. In conclusion, Cit-capped AgNPs had antibacterial activity against multiple drug resistant (MDR) A. baumannii but not against K. pneumoniae and E. coli. Cit-capped AgNPs increased the inhibition zone of imipenem in additive effect; the minimum inhibitory concentration and the minimum bactericidal concentration of Citcapped AgNPs were relatively low. Cit-capped AgNPs eliminated A. baumannii infection in vivo when it was given alone or in combination with imipenem. The cytotoxicity of Cit-AgNPs was dosedependent and the organs differed in the illumination of the inflammatory effect of Cit-AgNPs after high dose administration. It is not recommended to use Cit-capped AgNPs systemically despite their valuable additive antibacterial effect especially with a high dose and the combination with imipenem, Topical administration needs to be evaluated.
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Nano Biomedicine and Engineering
Nano Biomedicine and Engineering Engineering-Biomedical Engineering
CiteScore
3.00
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0.00%
发文量
9
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