A self-loading microfluidic device for determining the minimum inhibitory concentration of antibiotics

被引:116
作者
Cira, Nate J. [1 ]
Ho, Jack Y. [1 ]
Dueck, Megan E. [2 ]
Weibel, Douglas B. [1 ,3 ]
机构
[1] Univ Wisconsin Madison, Dept Biomed Engn, Madison, WI 53706 USA
[2] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[3] Univ Wisconsin Madison, Dept Biochem, Madison, WI 53706 USA
关键词
SUSCEPTIBILITY; RESISTANCE; MECHANISMS; CARTRIDGES; FUTURE; PLUGS;
D O I
10.1039/c2lc20887c
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This article describes a portable microfluidic technology for determining the minimum inhibitory concentration (MIC) of antibiotics against bacteria. The microfluidic platform consists of a set of chambers molded in poly(dimethylsiloxane) (PDMS) that are preloaded with antibiotic, dried, and reversibly sealed to a second layer of PDMS containing channels that connect the chambers. The assembled device is degassed via vacuum prior to its use, and the absorption of gas by PDMS provides the mechanism for actuating and metering the flow of fluid in the microfluidic channels and chambers. During the operation of the device, degas driven flow introduces a suspension of bacterial cells, dissolves the antibiotic, and isolates cells in individual chambers without cross contamination. The growth of bacteria in the chambers in the presence of a pH indicator produces a colorimetric change that can be detected visually using ambient light. Using this device we measured the MIC of vancomycin, tetracycline, and kanamycin against Enterococcus faecalis 1131, Proteus mirabilis HI4320, Klebsiella pneumoniae, and Escherichia coli MG1655 and report values that are comparable to standard liquid broth dilution measurements. The device provides a simple method for MIC determination of individual antibiotics against human pathogens that will have applications for clinical and point-of-care medicine. Importantly, this device is designed around simplicity: it requires a single pipetting step to introduce the sample, no additional components or external equipment for its operation, and provides a straightforward visual measurement of cell growth. As the device introduces a novel approach for filling and isolating dead-end microfluidic chambers that does not require valves and actuators, this technology should find applications in other portable assays and devices.
引用
收藏
页码:1052 / 1059
页数:8
相关论文
共 26 条
[1]   Production of arrays of chemically distinct nanolitre plugs via repeated splitting in microfluidic devices [J].
Adamson, David N. ;
Mustafi, Debarshi ;
Zhang, John X. J. ;
Zheng, Bo ;
Ismagilov, Rustem F. .
LAB ON A CHIP, 2006, 6 (09) :1178-1186
[2]   MECHANISMS OF ANTIBIOTIC-RESISTANCE IN BACTERIA [J].
BENVENISTE, R ;
DAVIES, J .
ANNUAL REVIEW OF BIOCHEMISTRY, 1973, 42 :471-506
[3]   Detecting bacteria and determining their susceptibility to antibiotics by stochastic confinement in nanoliter droplets using plug-based microfluidics [J].
Boedicker, James Q. ;
Li, Liang ;
Kline, Timothy R. ;
Ismagilov, Rustem F. .
LAB ON A CHIP, 2008, 8 (08) :1265-1272
[4]   Antimicrobial Susceptibility Testing Using High Surface-to-Volume Ratio Microchannels [J].
Chen, Chia Hsiang ;
Lu, Yi ;
Sin, Mandy L. Y. ;
Mach, Kathleen E. ;
Zhang, Donna D. ;
Gau, Vincent ;
Liao, Joseph C. ;
Wong, Pak Kin .
ANALYTICAL CHEMISTRY, 2010, 82 (03) :1012-1019
[5]   Microfluidic cartridges preloaded with nanoliter plugs of reagents: an alternative to 96-well plates for screening [J].
Chen, Delai L. ;
Ismagilov, Rustem F. .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2006, 10 (03) :226-231
[6]   Lab-on-a-chip devices for global health: Past studies and future opportunities [J].
Chin, Curtis D. ;
Linder, Vincent ;
Sia, Samuel K. .
LAB ON A CHIP, 2007, 7 (01) :41-57
[7]  
Dimov IK, 2011, LAB CHIP, V11, P845, DOI [10.1039/c0lc00403k, 10.1039/c01c00403k]
[8]   Rapid prototyping of microfluidic systems in poly(dimethylsiloxane) [J].
Duffy, DC ;
McDonald, JC ;
Schueller, OJA ;
Whitesides, GM .
ANALYTICAL CHEMISTRY, 1998, 70 (23) :4974-4984
[9]   Encapsulating Bacteria in Agarose Microparticles Using Microfluidics for High-Throughput Cell Analysis and Isolation [J].
Eun, Ye-Jin ;
Utada, Andrew S. ;
Copeland, Matthew F. ;
Takeuchi, Shoji ;
Weibel, Douglas B. .
ACS CHEMICAL BIOLOGY, 2011, 6 (03) :260-266
[10]   Comparison of the Etest and agar dilution for in vitro antimicrobial susceptibility testing of Campylobacter [J].
Ge, B ;
Bodeis, S ;
Walker, RD ;
White, DG ;
Zhao, S ;
McDermott, PF ;
Meng, JH .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 50 (04) :487-494