Issue 23, 2024

Self-actuated microfluidic chiplet for two-stage multiplex nucleic acid amplification assay

Abstract

Effective diagnosis of comorbidities and infectious diseases that present similar symptoms requires point-of-need assays capable of co-detecting and differentiating among multiple co-endemic pathogens to enable timely, precision medicine and effective control measures. We previously developed a two-stage isothermal amplification assay dubbed Penn-RAMP to address this need. Penn-RAMP's first stage comprises a recombinase polymerase amplification (RPA), which amplifies all targets of interest in a single reaction chamber for a short duration. The RPA amplicons are then aliquoted into multiple loop-mediated isothermal amplification (LAMP) reaction chambers, each customized with pre-dried primers to amplify a single target or a group of targets. To enable Penn-RAMP at the point of need, we describe here a self-actuated Penn-RAMP chiplet that accommodates the Penn-RAMP assay. Our chiplet employs temperature-controlled phase change valves and capillary valves to self-aliquot first-stage amplicons into multiple (five) second-stage reaction chambers and to seal these chambers. The functionality of our device is demonstrated by co-detecting plant pathogens. The analytical performance of our chiplet is comparable to that of the benchtop Penn-RAMP assay and surpasses that of standalone LAMP assays. Our self-actuated chiplet can be operated standalone with purified nucleic acids or as the downstream amplification module of a sample preparation cassette.

Graphical abstract: Self-actuated microfluidic chiplet for two-stage multiplex nucleic acid amplification assay

Supplementary files

Article information

Article type
Paper
Submitted
10 Sep 2024
Accepted
21 Oct 2024
First published
22 Oct 2024
This article is Open Access
Creative Commons BY-NC license

Lab Chip, 2024,24, 5175-5183

Self-actuated microfluidic chiplet for two-stage multiplex nucleic acid amplification assay

F. Ansah, M. Hajialyani, F. Ahmadi, Y. Gu, E. A. Tarım, M. G. Mauk, G. A. Awandare and H. H. Bau, Lab Chip, 2024, 24, 5175 DOI: 10.1039/D4LC00752B

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