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Functionalised nanoparticles complexed with antibiotic efficiently kill MRSA and other bacteria.
Wang, Lei; Chen, Yung Pin; Miller, Kristen P; Cash, Brandon M; Jones, Shonda; Glenn, Steven; Benicewicz, Brian C; Decho, Alan W.
Afiliação
  • Wang L; Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA.
Chem Commun (Camb) ; 50(81): 12030-3, 2014 Oct 18.
Article em En | MEDLINE | ID: mdl-25136934
ABSTRACT
Antibiotic-resistant bacterial infections are a vexing global health problem and have rendered ineffective many previously-used antibiotics. Here we demonstrate that antibiotic-linkage to surface-functionalized silica nanoparticles (sNP) significantly enhances their effectiveness against Escherichia coli, and Staphylococcus aureus, and even methicillin-resistant S. aureus (MRSA) strains that are resistant to most antibiotics. The commonly-used antibiotic penicillin-G (PenG) was complexed to dye-labeled sNPs (15 nm diameter) containing carboxyl groups located as either surface-functional groups, or on polymer-chains extending from surfaces. Both sNPs configurations efficiently killed bacteria, including MRSA strains. This suggests that activities of currently-ineffective antibiotics can be restored by nanoparticle-complexation and used to avert certain forms of antibiotic-resistance.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanopartículas / Staphylococcus aureus Resistente à Meticilina / Antibacterianos Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanopartículas / Staphylococcus aureus Resistente à Meticilina / Antibacterianos Idioma: En Ano de publicação: 2014 Tipo de documento: Article