Decentralized molecular detection of pathogens remains an important goal for public health. Although polymerase chain reaction (PCR) remains the gold-standard molecular detection method, thermocycling using Peltier heaters presents challenges in decentralized settings. Recent work has demonstrated plasmonic PCR, where nanomaterials on a surface or nanoparticles in solution heat upon stimulation by light, as a promising method for rapid thermocycling. Heating of a solution via nanoparticles suspended in solution has been demonstrated in PCR tubes, but not on microfluidic chips. We developed a volumetric, microfluidic plasmonic reverse transcription (RT)-PCR method. A microfluidic chip is fabricated with an integrated thermocouple to measure internal temperature, feeding into a proportional-integral-derivative (PID) algorithm that modulates an infrared LED for closed-loop control. Gold nanorods are dispersed in solution with RT-PCR reagents. We created an instrument for plasmonic RT-PCR using an infrared LED for heating, fan for cooling, and fluorometer for end-point fluorescence detection. Rapid thermocycling and amplification of SARS-CoV-2 within 16 min (5 min for RT, 45 cycles in 11 min) is achieved. This paper demonstrates volumetric, plasmonic PCR in a microfluidic chip, using an integrated thermocouple for closed-loop control. This work points to the promise of using microfluidics and nanomaterials to achieve rapid, compact detection of pathogens in decentralized settings.
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http://dx.doi.org/10.1002/smtd.202401988 | DOI Listing |
Small Methods
March 2025
Department of Biomedical Engineering, Columbia University, New York, NY, 10027, USA.
Decentralized molecular detection of pathogens remains an important goal for public health. Although polymerase chain reaction (PCR) remains the gold-standard molecular detection method, thermocycling using Peltier heaters presents challenges in decentralized settings. Recent work has demonstrated plasmonic PCR, where nanomaterials on a surface or nanoparticles in solution heat upon stimulation by light, as a promising method for rapid thermocycling.
View Article and Find Full Text PDFMacromol Rapid Commun
March 2025
Department of Mechanical Engineering, York University, Toronto, ON, M3J 1P3, Canada.
Investigating the swelling behavior of superabsorbent polymer microparticles (SAP-MPs) at a single-particle level using traditional methods is constrained by low resolution and insufficient real-time data, especially for particles smaller than 300 µm. To address these challenges, a novel microfluidic device capable is developed of real-time, high-precision single-particle analysis. This platform hydrodynamically traps individual SAP-MPs, enabling continuous monitoring of their swelling dynamics under controlled conditions.
View Article and Find Full Text PDFAPL Bioeng
March 2025
Key Laboratory of Biorheological Science and Technology, Ministry of Education and Bioengineering College, Chongqing University, Chongqing 400044, China.
Cell fusion is a widely employed process in various biological procedures, demonstrating significant application value in biotechnology. Cell pairing is a crucial manipulation for cell fusion. Standard fusion techniques, however, often provide poor and random cell contact, leading to low yields.
View Article and Find Full Text PDF3D Print Addit Manuf
December 2024
Department of Mechanical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan.
Proc Natl Acad Sci U S A
December 2024
Mechanobiology Institute, National University of Singapore, 117411, Singapore.
Diverse tissues in vivo present varying degrees of confinement, constriction, and compression to migrating cells in both homeostasis and disease. The nucleus in particular is subjected to external forces by the physical environment during confined migration. While many systems have been developed to induce nuclear deformation and analyze resultant functional changes, much remains unclear about dynamic volume regulation in confinement due to limitations in time resolution and difficulty imaging in PDMS-based microfluidic chips.
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