利奈唑啉
杀生物剂
抗菌剂
背景(考古学)
最小抑制浓度
等结构
抗生素
微生物学
材料科学
化学
生物
细菌
金黄色葡萄球菌
万古霉素
有机化学
古生物学
晶体结构
遗传学
作者
Dalia Ramos,Javier Águila-Rosas,Carlos Tomás Quirino-Barreda,Alfonso Santiago-Téllez,Hugo A. Lara-García,Ariel Guzmán‐Vargas,Ilich A. Ibarra,Enrique Lima
摘要
Linezolid (LNZ) is a new-generation synthetic molecule for the antibacterial treatment of severe infections, particularly in infective cases where the bacterial resistance to first-choice drugs is caused by Gram-positive pathogens. In this context, since 2009, some strains resistant to LNZ in patients with long-term treatments have been reported. Therefore, there is a need to use not only new drug molecules with antibacterial activities in the dosage form but also a different approach to pharmacotherapeutic strategies for skin infections, which lead to a reduction in the concentration of biocides. This work explores LNZ hosted at two isostructural MOFs, MOF-74(Zn) and MOF-74(Cu), as promising antimicrobial systems for gradual biocide release within 6 h. These systems reach a lower minimum inhibitory concentration (MIC) in comparison to free LNZ. Even a decreased MIC value is also observed, which is an encouraging result regarding the efficiency of the systems to control concentration-dependent antimicrobial resistance.
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