4.8 Article

Acoustofluidics and Whole-Blood Manipulation in Surface Acoustic Wave Counterflow Devices

期刊

ANALYTICAL CHEMISTRY
卷 86, 期 21, 页码 10633-10638

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AMER CHEMICAL SOC
DOI: 10.1021/ac502465s

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  1. CNR project: NANOMAX Nanotechnology-based therapy and diagnostics of brain diseases-NANOBRAIN

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On-chip functional blocks for sample preprocessing are necessary elements for the implementation of fully portable micrototal analysis systems (mu TAS). We demonstrate and characterize the microparticle and whole-blood manipulation capabilities of surface acoustic wave (SAW) driven counterflow micropumps. The motion of suspended cells in this system is governed by the two dominant acoustic forces associated with the scattered SAW (of wavelength ?f): acoustic-radiation force and acoustic-streaming Stokesian drag force. We show that by reducing the microchannel height (h) beyond a threshold value the balance of these forces is shifted toward the acoustic-radiation force and that this yields control of two different regimes of microparticle dynamics. In the regime dominated by the acoustic radiation force (h less than or similar to f), microparticles are collected in the seminodes of the partial standing sound-wave arising from reflections off microchannel walls. This enables the complete separation of plasma and corpuscular components of whole blood in periodical predetermined positions without any prior sample dilution. Conversely, in the regime dominated by acoustic streaming (h less than or similar to f), the microbeads follow vortical streamlines in a pattern characterized by three different phases during microchannel filling. This makes it possible to generate a cell-concentration gradient within whole-blood samples, a behavior not previously reported in any acoustic-streaming device. By careful device design, a new class of SAW pumping devices is presented that allows the manipulation and pretreatment of whole-blood samples for portable and integrable biological chips and is compatible with hand-held battery-operated devices.

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