用于原位光学分析的标准96孔基高通量微流体灌注生物膜反应器。

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL
David McLeod, Lai Wei, Zhenyu Li
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引用次数: 0

摘要

生物膜感染是一个主要的公共健康威胁,因为它们对抗菌药物的高耐受性和缺乏特定的抗生物膜药物。为了开发这种药物,至关重要的是要有高通量的生物膜生长系统,能够模拟体内条件,而不需要动物模型的成本和复杂性。然而,目前没有一种生物膜反应器能够以高通量标准微量滴定仪的形式提供类似体内的条件。本文展示了一种新型的高通量(HT)微流体灌注生物膜反应器(HT-μPBR),该反应器与用于原位光学分析的标准96孔微量滴定板兼容。设计并制造了一种用于标准微量滴定板的卡扣式液体密封盖,该盖具有流体通道,以提供闭环循环灌注。我们的系统采取步骤,提供类似体内的条件,控制剪切应力和养分输送。我们描述了系统的制造和在大肠杆菌(E.coli)生物膜的生物量和活力的光学分析中的使用。HT-μPBR设置为以1 mL/min的速度灌注,对应于单个孔底表面上约[公式:见正文]的平均剪切速率。在孔板底部检测生物膜,并使用荧光显微镜和读板器进行测量,以确定生物量和活力。在HT-μPBR中培养的样品显示生物量增加,同时在24小时后保持活力。HT-μPBR可以进一步与HT抗生素敏感性测试和延时成像等额外的光学技术相结合,以提高对药物反应机制的理解,并优化药物组合和递送谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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-μPBR) 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-μPBR was set to perfuse at 1 mL/min corresponding to an average shear rate of approximately \(5.7{\mathrm{s}}^{-1}\) 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-μPBR showed increased biomass while maintaining viability after 24 h. The HT-μPBR 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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来源期刊
Biomedical Microdevices
Biomedical Microdevices 工程技术-工程:生物医学
CiteScore
6.90
自引率
3.60%
发文量
32
审稿时长
6 months
期刊介绍: Biomedical Microdevices: BioMEMS and Biomedical Nanotechnology is an interdisciplinary periodical devoted to all aspects of research in the medical diagnostic and therapeutic applications of Micro-Electro-Mechanical Systems (BioMEMS) and nanotechnology for medicine and biology. General subjects of interest include the design, characterization, testing, modeling and clinical validation of microfabricated systems, and their integration on-chip and in larger functional units. The specific interests of the Journal include systems for neural stimulation and recording, bioseparation technologies such as nanofilters and electrophoretic equipment, miniaturized analytic and DNA identification systems, biosensors, and micro/nanotechnologies for cell and tissue research, tissue engineering, cell transplantation, and the controlled release of drugs and biological molecules. Contributions reporting on fundamental and applied investigations of the material science, biochemistry, and physics of biomedical microdevices and nanotechnology are encouraged. A non-exhaustive list of fields of interest includes: nanoparticle synthesis, characterization, and validation of therapeutic or imaging efficacy in animal models; biocompatibility; biochemical modification of microfabricated devices, with reference to non-specific protein adsorption, and the active immobilization and patterning of proteins on micro/nanofabricated surfaces; the dynamics of fluids in micro-and-nano-fabricated channels; the electromechanical and structural response of micro/nanofabricated systems; the interactions of microdevices with cells and tissues, including biocompatibility and biodegradation studies; variations in the characteristics of the systems as a function of the micro/nanofabrication parameters.
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