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Nanoliter-Sized Microchamber/Microarray Microfluidic Platform for Antibiotic Susceptibility Testing.
Azizi, Morteza; Zaferani, Meisam; Dogan, Belgin; Zhang, Shiying; Simpson, Kenneth W; Abbaspourrad, Alireza.
Afiliación
  • Azizi M; Department of Food Science, College of Agricultural and Life Sciences , Cornell University , Ithaca , New York 14853 , United States.
  • Zaferani M; Department of Food Science, College of Agricultural and Life Sciences , Cornell University , Ithaca , New York 14853 , United States.
  • Dogan B; Department of Clinical Sciences, College of Veterinary Medicine , Cornell University , Ithaca , New York 14853 , United States.
  • Zhang S; Department of Clinical Sciences, College of Veterinary Medicine , Cornell University , Ithaca , New York 14853 , United States.
  • Simpson KW; Department of Clinical Sciences, College of Veterinary Medicine , Cornell University , Ithaca , New York 14853 , United States.
  • Abbaspourrad A; Department of Food Science, College of Agricultural and Life Sciences , Cornell University , Ithaca , New York 14853 , United States.
Anal Chem ; 90(24): 14137-14144, 2018 12 18.
Article en En | MEDLINE | ID: mdl-30474959
ABSTRACT
The rise of antimicrobial resistance is challenging for physicians in clinical practice to prescribe antibiotics that are effective against bacterial infections. Conventional antibiotic susceptibility testing (AST) is labor-intensive and time-consuming (18-24 h). Newly emerging technologies such as microfluidics may enable more rapid AST assay time. In this study, we utilize a nanoliter-sized microchamber/microarray-based microfluidic (N-3M) platform to reduce the AST assay time and rapidly determine the minimum inhibitory concentrations of different antibiotics. Bacterial suspensions, with or without antibiotics, are loaded into small nanoliter-sized chambers, and the change in fluorescent intensity emitted from resazurin reduction, which correlated with bacterial growth, is measured. We demonstrate the reproducibility, functionality, and efficiency of our N-3M platform for numerous wild-type clinical bacterial isolates including Escherichia coli, Klebsiella pneumoniae, and Enterococcus faecalis. The time-to-result of our N-3M platform varies between ∼1-3 h, depending on growth rates of different bacterial species. We believe that our proposed N-3M platform is robust, is easy-to-implement, has a short time-to-result, and can be applicable for microbial AST in clinical applications.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Bacterias / Pruebas de Sensibilidad Microbiana / Microfluídica / Antibacterianos Idioma: En Revista: Anal Chem Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Bacterias / Pruebas de Sensibilidad Microbiana / Microfluídica / Antibacterianos Idioma: En Revista: Anal Chem Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos