De Maio Flavio, Palmieri Valentina, Santarelli Giulia, Perini Giordano, Salustri Alessandro, Palucci Ivana, Sali Michela, Gervasoni Jacopo, Primiano Aniello, Ciasca Gabriele, Sanguinetti Maurizio, De Spirito Marco, Delogu Giovanni, Papi Massimiliano
Dipartimento di Scienze di Laboratorio e Infettivologiche, Fondazione Policlinico Universitario "A. Gemelli" IRCSS, 00168 Rome, Italy.
Dipartimento di Scienze biotecnologiche di base, cliniche intensivologiche e perioperatorie-Sezione di Microbiologia, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Nanomaterials (Basel). 2020 Jul 22;10(8):1431. doi: 10.3390/nano10081431.
Global pandemic management represents a serious issue for health systems. In some cases, repurposing of existing medications might help find compounds that have the unexpected potential to combat microorganisms. In the same way, changing cell-drug interaction by nanotechnology could represent an innovative strategy to fight infectious diseases. Tuberculosis (TB) remains one of the most alarming worldwide infectious diseases and there is an urgent need for new drugs and treatments, particularly for the emergence and spread of drug-resistant () strains. New nanotechnologies based on carbon nanomaterials are now being considered to improve anti-TB treatments, and graphene oxide (GO) showed interesting properties as an anti-TB drug. GO, which preferentially accumulates in the lungs and is degraded by macrophagic peroxidases, can trap and in a dose-dependent manner, reducing the entry of bacilli into macrophages. In this paper, combinations of isoniazid (INH), amikacin (AMK) and linezolid (LZD) and GO anti-mycobacterial properties were evaluated against H37Rv by using a checkerboard assay or an in vitro infection model. Different GO effects have been observed when incubated with INH, AMK or LZD. Whereas the INH and AMK anti-mycobacterial activities were blocked by GO co-administration, the LZD bactericidal effect increased in combination with GO. GO-LZD significantly reduced extracellular mycobacteria during infection and was able to kill internalized bacilli. GO-LZD co-administration is potentially a new promising anti-TB treatment at the forefront in fighting emerging antibiotic-resistant strains where LZD administration is suggested. This innovative pharmacological approach may lead to reduced treatment periods and decreased adverse effects. More importantly, we demonstrate how nanomaterials-drugs combinations can represent a possible strategy to quickly design drugs for pandemics treatment.
全球大流行管理对卫生系统而言是一个严峻问题。在某些情况下,重新利用现有药物可能有助于找到具有对抗微生物意外潜力的化合物。同样,通过纳米技术改变细胞与药物的相互作用可能是对抗传染病的一种创新策略。结核病仍然是全球最令人担忧的传染病之一,迫切需要新的药物和治疗方法,尤其是针对耐药菌株的出现和传播。基于碳纳米材料的新型纳米技术目前正被考虑用于改善抗结核治疗,氧化石墨烯(GO)作为一种抗结核药物展现出了有趣的特性。GO优先在肺部积聚并被巨噬细胞过氧化物酶降解,它能以剂量依赖的方式捕获结核菌和其他物质,减少杆菌进入巨噬细胞。在本文中,通过棋盘法或体外感染模型评估了异烟肼(INH)、阿米卡星(AMK)和利奈唑胺(LZD)与GO的组合对结核分枝杆菌H37Rv的抗分枝杆菌特性。当与INH、AMK或LZD一起孵育时,观察到了不同的GO效应。虽然联合使用GO会阻断INH和AMK的抗分枝杆菌活性,但LZD与GO联合使用时杀菌效果增强。GO-LZD在感染期间显著减少了细胞外分枝杆菌,并能够杀死内化的杆菌。在建议使用LZD治疗新兴抗生素耐药菌株的前沿领域,联合使用GO-LZD可能是一种新的有前景的抗结核治疗方法。这种创新的药理学方法可能会缩短治疗周期并减少不良反应。更重要的是,我们展示了纳米材料与药物的组合如何可能成为快速设计大流行治疗药物的一种策略。