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Supramolecular antibiotics: a strategy for conversion of broad-spectrum to narrow-spectrum antibiotics for Staphylococcus aureus.
Koyasseril-Yehiya, Thameez M; García-Heredia, Alam; Anson, Francesca; Rangadurai, Poornima; Siegrist, M Sloan; Thayumanavan, S.
Afiliação
  • Koyasseril-Yehiya TM; Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, USA. thai@umass.edu.
  • García-Heredia A; Molecular and Cellular Biology Program, University of Massachusetts, Amherst, Massachusetts 01003, USA.
  • Anson F; Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, USA. thai@umass.edu.
  • Rangadurai P; Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, USA. thai@umass.edu.
  • Siegrist MS; Molecular and Cellular Biology Program, University of Massachusetts, Amherst, Massachusetts 01003, USA and Department of Microbiology, University of Massachusetts, Amherst, Massachusetts 01003, USA. siegrist@umass.edu and Models to Medicine, Institute for Applied Life Sciences, University of Massach
  • Thayumanavan S; Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, USA. thai@umass.edu and Molecular and Cellular Biology Program, University of Massachusetts, Amherst, Massachusetts 01003, USA and Models to Medicine, Institute for Applied Life Sciences, University of Massachusetts,
Nanoscale ; 12(40): 20693-20698, 2020 Oct 22.
Article em En | MEDLINE | ID: mdl-33029599
ABSTRACT
The propensity of broad-spectrum antibiotics to indiscriminately kill both pathogenic and beneficial bacteria has a profound impact on the spread of resistance across multiple bacterial species. Alternative approaches that narrow antibacterial specificity towards desired pathogenic bacterial population are of great interest. Here, we report an enzyme-responsive antibiotic-loaded nanoassembly strategy for narrow delivery of otherwise broad-spectrum antibiotics. We specifically target Staphylococcus aureus (S. aureus), an important blood pathogen that secretes PC1 ß-lactamases. Our nanoassemblies selectively eradicate S. aureus grown in vitro with other bacteria, highlighting its potential capability in targeting the desired pathogenic bacterial population.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções Estafilocócicas / Staphylococcus aureus Limite: Humans Idioma: En Revista: Nanoscale Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções Estafilocócicas / Staphylococcus aureus Limite: Humans Idioma: En Revista: Nanoscale Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos