粪肠球菌
抗生素
雷苏林
微流控
化学
肺炎克雷伯菌
微生物学
细菌生长
大肠杆菌
抗生素耐药性
细菌
纳米技术
生物
材料科学
生物化学
基因
遗传学
作者
Morteza Azizi,Meisam Zaferani,Belgin Dogan,Shiying Zhang,Kenneth W. Simpson,Alireza Abbaspourrad
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2018-11-26
卷期号:90 (24): 14137-14144
被引量:33
标识
DOI:10.1021/acs.analchem.8b03817
摘要
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.
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