A standard 96-well based high throughput microfluidic perfusion biofilm reactor for in situ optical analysis

被引:0
作者
McLeod, David [1 ]
Wei, Lai [1 ]
Li, Zhenyu [1 ]
机构
[1] George Washington Univ, Dept Biomed Engn, 800 22nd St NW, Washington, DC 20052 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Microfluidic; Biofilm; Bioreactor; Fabrication; Perfusion; RESISTANCE; CULTURE; CELLS;
D O I
10.1007/s10544-023-00668-w
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Biofilm infections represent a major public health threat due to their high tolerance to antimicrobials and the lack of specific anti-biofilm drugs. To develop such drugs, it is crucial to have high-throughput biofilm growth systems that can emulate in vivo conditions without the cost and complexity of animal models. However, no current biofilm reactor can provide in vivo-like conditions in a high throughput standard microtiter format. This paper demonstrates a novel high-throughput (HT) microfluidic perfusion biofilm reactor (HT-mu PBR) compatible with a standard 96-well microtiter plate for in situ optical analysis. A snap-on liquid-tight cover for standard microtiter plates was designed and fabricated with fluidic channels to provide closed-loop recirculating perfusion. Our system takes steps toward providing in vivo-like conditions with controlled shear stress and nutrient delivery. We describe the system fabrication and usage in optical analysis of biomass and viability of Escherichia coli (E. coli) biofilms. The HT-mu PBR was set to perfuse at 1 mL/min corresponding to an average shear rate of approximately 5.7s(-1) on the bottom surface of a single well. Biofilms were detected on well plate bottoms and measured using a fluorescence microscope and plate reader to determine biomass and viability. Samples cultured in the HT-mu PBR showed increased biomass while maintaining viability after 24 h. The HT-mu PBR can further be combined with HT antibiotic susceptibility testing and additional optical techniques such as time-lapse imaging to improve understanding of the drug reaction mechanism as well as the optimization of drug combinations and delivery profiles.
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页数:12
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