4.7 Article

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

Journal

LAB ON A CHIP
Volume 21, Issue 11, Pages 2223-2231

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1lc00216c

Keywords

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Funding

  1. Ministry of Science and Technology (MOST) of Taiwan [MOST 108-2314-B-007-002, MOST 1072221-E-007-013-MY3]
  2. National Health Research Institutes [NHRI-EX108-10828EI]

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The study developed a microfluidic platform for rapid antimicrobial susceptibility testing, including dilution of antibiotics and distribution of bacteria, which can improve efficiency and accuracy of the testing process.
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 (similar to 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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