A multiplexed nanoliter array-based microfluidic platform for quick, automatic antimicrobial susceptibility testing

微流控 纳米技术 微流控芯片 实验室晶片 多路复用 材料科学 流体学 生物芯片 生物传感器 计算机科学 多路复用 分析物 化学
作者
Mohammad Osaid,Yi-Sin Chen,Chih-Hung Wang,Anirban Sinha,Wen-Bin Lee,Priya Gopinathan,Hung-Bin Wu,Gwo-Bin Lee
出处
期刊:Lab on a Chip [Royal Society of Chemistry]
卷期号:21 (11): 2223-2231 被引量:2
标识
DOI:10.1039/d1lc00216c
摘要

Antimicrobial resistance stemming from indiscriminate usage of antibiotics has emerged as a global healthcare issue with substantial economic implications. The inefficacy of commonly used antibiotics combined with superfluous consumption has worsened the issue. Rapid antimicrobial susceptibility testing (AST) to antibiotics can be advantageous in thwarting bacterial infections. Therefore, this study developed a simple nanoliter array-based microfluidic platform for performing rapid AST, which can handle and manipulate liquids both in nanoliter and microliter volumes. The platform consisted of two microfluidic devices, one for performing AST and another for diluting antibiotics and these two were suitably integrated. The microfluidic device used for generating microarrays for AST experiments is single-layered (no air layer) and has no active microvalves and air hole, which makes the device easy to fabricate and use. The loading process ensures uniform distribution of bacteria and relies on displacing the air from microarrays through porous polydimethylsiloxane membranes. Furthermore, the chip for dilution consisted of active microfluidic components, and could prepare and test seven different concentrations of antibiotics, which make the platform multiplexed and be capable of evaluating minimum inhibitory concentrations (MICs), a clinically relevant parameter. MIC determination requires less number of bacteria (∼2000) and hence shortens the pre-culture step, i.e. bacteria culture in blood and urine. This automated system demonstrated AST and evaluated MICs using Escherichia coli and two antibiotics, including ampicillin and streptomycin, and the results were ascertained using a gold standard method. It only took 8-9 h to perform AST, which is substantially less compared to a conventional process and hence is of high clinical utility.

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