4.7 Article

A milliliter to picoliter-level centrifugal microfluidic concentrator for fast pathogen detection and antimicrobial susceptibility testing

Journal

SENSORS AND ACTUATORS B-CHEMICAL
Volume 343, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.130117

Keywords

Centrifugal microfluidics; Cephalosporin; Carbapenem; Antimicrobial susceptibility testing; Pathogen detection

Funding

  1. Strategic Priority Research Program of Chinese Academy of Sciences [XDB29050400]
  2. National Natural Science Foundation of China [21775155]
  3. Natural Science Foundation of Shandong, China [ZR2019PB022]
  4. Science and Technology Service Network Initiative Program of Chinese Academy of Sciences [KFJ-STS-QYZX-087]
  5. United Foundation of DICPQIBEBT, CAS [DICPQIBEBTUN201806]

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This study introduces a centrifugation-based microfluidic concentrator for rapid and real-time pathogen detection and antimicrobial susceptibility testing. By transferring pathogen cells from the loading chamber to the picoliter-level enrichment channel, high enrichment efficiency is achieved without traditional pre-culture steps.
The available pathogenic bacteria detection and antimicrobial susceptibility testing (AST) are still time-consuming and tedious because of the lengthy culture procedures. Various kinds of systems have promised a great reduction in AST time, however the high-efficiency and user-friendly bacteria enrichment is always a challenge to tackle. Here we introduce a centrifugation-based microfluidic concentrator for milliliter to picoliter bacteria suspension enrichment to achieve a fast and real-time pathogen detection and AST. The concentrator consists of a milliliter-level loading chamber and a picoliter-level enrichment channel. By centrifuging, all pathogen cells in chamber can be condensed into enrichment channel, achieving a milliliter to picoliter enrichment. Thus, the pathogen cells can be detected directly by microscopic observation. More importantly, the AST can be started from original sample without traditional pre-culture steps for the high enrichment efficiency. Since all the cells were confined at the picoliter-level channel tip, detectable growth of phenotype can be easily observed in a few hours, and the different inhibition mechanism on cells from different antibiotics can be clearly observed. The proposed concentrator shows a detection limit of 10(2) cell/mL with 0.5 h of enrichment for detection and another 3 h of micro-culture for AST.

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