Wireless dielectrophoresis trapping and remote impedance sensing via resonant wireless power transfer
Nearly all biosensing platforms can be described using two fundamental steps—collection and detection. Target analytes must be delivered to a sensing element, which can then relay the transduced signal. For point-of-care technologies, where operation is to be kept simple, typically the collection st...
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Veröffentlicht in: | Nature communications 2023-01, Vol.14 (1), p.103-9, Article 103 |
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Sprache: | eng |
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Zusammenfassung: | Nearly all biosensing platforms can be described using two fundamental steps—collection and detection. Target analytes must be delivered to a sensing element, which can then relay the transduced signal. For point-of-care technologies, where operation is to be kept simple, typically the collection step is passive diffusion driven—which can be slow or limiting under low concentrations. This work demonstrates an integration of both active collection and detection by using resonant wireless power transfer coupled to a nanogap capacitor. Nanoparticles suspended in deionized water are actively trapped using wireless dielectrophoresis and positioned within the most sensitive fringe field regions for wireless impedance-based detection. Trapping of 40 nm particles and larger is demonstrated using a 3.5 V
RMS
, 1 MHz radiofrequency signal delivered over a distance greater than 8 cm from the nanogap capacitor. Wireless trapping and release of 1 µm polystyrene beads is simultaneously detected in real-time over a distance of 2.5 cm from the nanogap capacitor. Herein, geometric scaling strategies coupled with optimal circuit design is presented to motivate combined collection and detection biosensing platforms amenable to wireless and/or smartphone operation.
The authors use resonant wireless power transfer to remotely trap and release nanoparticles in solution and detect their presence as a shift in impedance in real-time. This is accomplished using the extreme field confinement of a nanogap capacitor. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-022-35777-2 |