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Passive Mixing Capabilities of Micro- and Nanofibres When Used in Microfluidic Systems

机译:在微流体系统中使用时微纤维和纳米纤维的被动混合能力

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摘要

Nanofibres are increasingly being used in the field of bioanalytics due to their large surface-area-to-volume ratios and easy-to-functionalize surfaces. To date, nanofibres have been studied as effective filters, concentrators, and immobilization matrices within microfluidic devices. In addition, they are frequently used as optical and electrochemical transduction materials. In this work, we demonstrate that electrospun nanofibre mats cause appreciable passive mixing and therefore provide dual functionality when incorporated within microfluidic systems. Specifically, electrospun nanofibre mats were integrated into Y-shaped poly(methyl methacrylate) microchannels and the degree of mixing was quantified using fluorescence microscopy and ImageJ analysis. The degree of mixing afforded in relationship to fibre diameter, mat height, and mat length was studied. We observed that the most mixing was caused by small diameter PVA nanofibres (450–550 nm in diameter), producing up to 71% mixing at the microchannel outlet, compared to up to 51% with polystyrene microfibres (0.8–2.7 μm in diameter) and 29% mixing in control channels containing no fibres. The mixing afforded by the PVA nanofibres is caused by significant inhomogeneity in pore size and distribution leading to percolation. As expected, within all the studies, fluid mixing increased with fibre mat height, which corresponds to the vertical space of the microchannel occupied by the fibre mats. Doubling the height of the fibre mat led to an average increase in mixing of 14% for the PVA nanofibres and 8% for the PS microfibres. Overall, mixing was independent of the length of the fibre mat used (3–10 mm), suggesting that most mixing occurs as fluid enters and exits the fibre mat. The mixing effects observed within the fibre mats were comparable to or better than many passive mixers reported in literature. Since the nanofibre mats can be further functionalized to couple analyte concentration, immobilization, and detection with enhanced fluid mixing, they are a promising nanomaterial providing dual-functionality within lab-on-a-chip devices.
机译:纳米纤维由于其大的表面积/体积比和易于功能化的表面,正越来越多地用于生物分析领域。迄今为止,已经研究了纳米纤维作为微流体装置中的有效过滤器,浓缩器和固定基质。另外,它们经常用作光学和电化学转导材料。在这项工作中,我们证明了电纺纳米纤维毡片会引起明显的被动混合,因此在微流体系统中结合时可提供双重功能。具体而言,将电纺纳米纤维毡整合到Y形聚甲基丙烯酸甲酯微通道中,并使用荧光显微镜和ImageJ分析定量混合程度。研究了与纤维直径,毡垫高度和毡垫长度相关的混合程度。我们观察到,最大的混合是由小直径的PVA纳米纤维(直径450-550 nm)引起的,在微通道出口处混合率高达71%,而聚苯乙烯微纤维(直径0.8-2.7μm)则高达51%。和29%在不含纤维的控制通道中混合。 PVA纳米纤维提供的混合是由孔径和分布中的显着不均匀性导致渗滤引起的。不出所料,在所有研究中,流体混合随着纤维垫高度的增加而增加,纤维垫高度对应于纤维垫所占据的微通道的垂直空间。纤维垫的高度加倍导致PVA纳米纤维的混合平均增加14%,而PS微纤维的混合平均增加8%。总体而言,混合与所用纤维垫的长度(3-10 mm)无关,这表明大多数混合是在流体进出纤维垫时发生的。在纤维垫内观察到的混合效果与文献中报道的许多无源混合器相当或更好。由于纳米纤维垫可以进一步功能化以结合分析物浓度,固定化和增强流体混合的检测功能,因此它们是一种有前途的纳米材料,可在芯片实验室设备中提供双重功能。

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