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1.
Microbiol Spectr ; 11(6): e0193023, 2023 Dec 12.
Artigo em Inglês | MEDLINE | ID: mdl-37861330

RESUMO

IMPORTANCE: Multi-drug resistance (MDR) by virtue of evolving resistance and virulence mechanisms among A. baumannii is a global concern which is responsible for lethal hospital-acquired infections. Therefore, it is crucial to develop new therapeutics against it. Metal complexes are compact structures with diverse mechanisms that the pathogens cannot evade easily which make them a strong drug candidate. In this study, we assessed the in vitro and in vivo efficacy of lithium complex {[Li(phen)2 sal]} against biofilm-forming MDR A. baumannii. The lithium complex displayed strong antimicrobial activity and reduced the pre-formed mature biofilm which is key barrier for antimicrobial action. Moreover, it employs oxidative stress as one of its mode of actions and causes cellular rupturing. Lithium complex was non-toxic and was significantly effective to overcome pneumonia in mice model. These results highlight the untapped potential of metal complexes that can be explored and utilized for combating notorious A. baumannii infections.


Assuntos
Infecções por Acinetobacter , Acinetobacter baumannii , Anti-Infecciosos , Complexos de Coordenação , Animais , Camundongos , Antibacterianos/farmacologia , Antibacterianos/uso terapêutico , Lítio/farmacologia , Farmacorresistência Bacteriana Múltipla , Complexos de Coordenação/farmacologia , Infecções por Acinetobacter/tratamento farmacológico , Anti-Infecciosos/farmacologia , Biofilmes , Testes de Sensibilidade Microbiana
2.
Int J Nanomedicine ; 14: 3983-3993, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31213810

RESUMO

Background: Infections caused by drug resistant bacteria are a major health concern worldwide and have prompted scientists to carry out efforts to overcome this challenge. Researchers and pharmaceutical companies are trying to develop new kinds of antimicrobial agents by using different physical and chemical methods to overcome these problems. Materials and methods: In the present study, rifampicin conjugated silver (Rif-Ag) nanoparticles have successfully been synthesized using a chemical method. Characterization of the nanoparticles was performed using a UV-Vis spectrophotometer, FTIR, SEM, TEM, and AFM. Results: The AFM, SEM, and TEM results showed that the average particle size of Rif-Ag nanoparticles was about 15-18±4 nm. The FTIR spectra revealed the conjugation of -NH2 and -OH functional moiety with silver nanoparticles surface. Considering the penetrating power of rifampicin, the free drug is compared with synthesized nanoparticle for antimicrobial, biofilm inhibition, and eradication potential. Synthesized nanoparticles were found to be significantly active as compared to drug alone. Conclusion: This study has shown greater biofilm inhibitory and eradicating potential against methicillin resistant Staphylococcus aureus and Klebsiella pneumoniae, as evident by crystal violet, MTT staining, and microscopic analysis. So, it will be further modified, and studies for the mechanism of action are needed.


Assuntos
Biofilmes/efeitos dos fármacos , Klebsiella pneumoniae/fisiologia , Nanopartículas Metálicas/química , Staphylococcus aureus Resistente à Meticilina/fisiologia , Rifampina/farmacologia , Prata/farmacologia , Antibacterianos/farmacologia , Temperatura Alta , Humanos , Concentração de Íons de Hidrogênio , Klebsiella pneumoniae/efeitos dos fármacos , Nanopartículas Metálicas/ultraestrutura , Staphylococcus aureus Resistente à Meticilina/efeitos dos fármacos , Testes de Sensibilidade Microbiana , Rifampina/química , Sais , Prata/química , Espectroscopia de Infravermelho com Transformada de Fourier
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