摘要
以含3,5-二正丁氧基苯基取代邻菲啰啉衍生物(DBPIP)为主配体合成了一个多吡啶钌配合物Ru-1。通过最低抑菌浓度、时间杀伤曲线、生物被膜实验、耐药性评价等探索了钌化合物对金黄色葡萄球菌的抗菌活性。通过大蜡螟幼虫感染模型研究了Ru-1的体内抗菌活性。结果表明,此钌配合物对金黄色葡萄球菌具有优良的抗菌活性。
A polypyridine ruthenium complexes were synthesized with 3,5-di-butyxyphenyl derivatives as the main ligand(DBPIP):Ru-1.The antibacterial activities of ruthenium complexes against S.aureus was evaluated by the minimum inhibitory concentration,time killing curve,biofilm experiments and drug resistance study experiments.The antibacterial activity of Ru-1 was investigated by the model of infection.The results showed that this ruthenium complexes showed excellent antibacterial activity against S.aureus.
作者
陈则文
熊艳师
廖向文
王金涛
Chen Zewen;Xiong Yanshi;Liao Xiangwen;Wang Jintao(School of Pharmacy,Jiangxi Science&Technology Normal University,Nanchang 330013,China)
出处
《广东化工》
CAS
2024年第4期34-36,共3页
Guangdong Chemical Industry
基金
国家自然科学基金(22067007,22067006)。
关键词
钌配合物
抗菌活性
抗菌机制
生物安全性
金黄色葡萄球菌
ruthenium complex
antibacterial activity
antibacterial mechanism
Biosafety
Staphylococcus aureus