四环素
流出
细菌
共轭体系
抗生素
化学
纳米颗粒
膜
碳纤维
微生物学
生物物理学
纳米技术
材料科学
生物化学
生物
有机化学
复合数
复合材料
聚合物
遗传学
作者
Tak H. Kim,Asim Raiz,Aradhana Devi Unni,Shweta Murhekar,Bogdan C. Donose,Matthias Floetenmeyer,Ian Edwin Cock,Christopher L. Brown
标识
DOI:10.1002/adbi.202000074
摘要
Nontoxic carbon nanoparticle samples prepared by both bottom-up and top-down approaches do not inhibit Gram-negative bacterial growth, indicating excellent biocompatibilities. However, cell growth inhibitory efficacies increase considerably when the carbon nanoparticles are conjugated with the antibiotic tetracycline. In tetracycline-resistant bacteria, these efficacies can approach tenfold higher activities when compared to tetracycline alone. No structural abnormality such as membrane disruptions is evident in the tested bacterial strains; this is in contrast with other nanocarbon systems such as graphene oxides, carbon nanotubes, and amine-functionalized carbon nanoparticles which do exhibit membrane disruptions. In comparison, the tetracycline-conjugated carbon nanoparticles induce membrane perturbations (but not membrane disruptions), inhibiting bacterial efflux mechanisms. It is proposed that when tetracycline is conjugated to the surface of carbon nanoparticles, it functions to direct the nanoparticles to membrane-associated tetracycline efflux pumps, thereby blocking and subsequently inhibiting their function. The conjugation between biocompatible carbon nanoparticles and subtherapeutic but well-established antibiotic molecules may provide hybrid antibiotic assembly strategies resulting in effective multidrug efflux inhibition for combating antibiotic resistance.
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