四环素
抗生素
细菌
抗生素耐药性
抗菌剂
细胞毒性
化学
微生物学
四环素类抗生素
细菌细胞结构
生物
体外
生物化学
遗传学
作者
Larissa Brentano Capeletti,Luciane F. de Oliveira,Kaliandra de Almeida Gonçalves,Jessica Fernanda Affonso de Oliveira,Ângela Saito,Jörg Kobarg,João Henrique Zimnoch dos Santos,Mateus Borba Cardoso
出处
期刊:Langmuir
[American Chemical Society]
日期:2014-06-05
卷期号:30 (25): 7456-7464
被引量:107
摘要
New and more aggressive antibiotic resistant bacteria arise at an alarming rate and represent an ever-growing challenge to global health care systems. Consequently, the development of new antimicrobial agents is required to overcome the inefficiency of conventional antibiotics and bypass treatment limitations related to these pathologies. In this study, we present a synthesis protocol, which was able to entrap tetracycline antibiotic into silica nanospheres. Bactericidal efficacy of these structures was tested against bacteria that were susceptible and resistant to antibiotics. For nonresistant bacteria, our composite had bactericidal efficiency comparable to that of free-tetracycline. On the other hand, the synthesized composites were able to avoid bacterial growth of resistant bacteria while free-tetracycline has shown no significant bactericidal effect. Finally, we have investigated the cytotoxicity of these nanoparticles against mammalian cells to check any possible poisoning effect. It was found that these nanospheres are not apoptosis-inducers and only a reduction on the cell replication rate was seen when compared to the control without nanoparticles.
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