2013
DOI: 10.1007/s10404-013-1166-0
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Mapping low-Reynolds-number microcavity flows using microfluidic screening devices

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Cited by 27 publications
(34 citation statements)
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“…techniques, low Reynolds number flows in microchannels with microcavities are attractive for precisely controlling of flow behaviors and establishing appropriate cell culture conditions, due to the unique hydrodynamic flow behaviors and the special structure of the microcavities (Fishler et al 2013;Karimi et al 2013;Liu et al 2008Liu et al , 2009Nilsson et al 2009;Tanyeri and Schroeder 2013;Yew et al 2013;Yu et al 2005). Furthermore, microcavity flows have many other promising abilities to mimic in vivo microenvironment, to use small quantities of samples/reagents, to be fabricated easily, to easily make heterogeneous cellular environment with multiplexing assay, and to analyze cellular information at the single-cell level (Yun et al 2013).…”
Section: Introductionmentioning
confidence: 97%
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“…techniques, low Reynolds number flows in microchannels with microcavities are attractive for precisely controlling of flow behaviors and establishing appropriate cell culture conditions, due to the unique hydrodynamic flow behaviors and the special structure of the microcavities (Fishler et al 2013;Karimi et al 2013;Liu et al 2008Liu et al , 2009Nilsson et al 2009;Tanyeri and Schroeder 2013;Yew et al 2013;Yu et al 2005). Furthermore, microcavity flows have many other promising abilities to mimic in vivo microenvironment, to use small quantities of samples/reagents, to be fabricated easily, to easily make heterogeneous cellular environment with multiplexing assay, and to analyze cellular information at the single-cell level (Yun et al 2013).…”
Section: Introductionmentioning
confidence: 97%
“…The demand for fine and precise control of microscale fluid flows in microfluidic devices for different applications, such as cell and particle trapping Park et al 2010;Mach et al 2011), sorting (Park et al 2009;Mu et al 2013), alignment (Nilsson et al 2009;Fan et al 2014), and separating target cells from heterogeneous cell solution (Yun et al 2013;Sackmann et al 2014;Zhou et al 2013), has become a central research theme in microfluidic systems (Fishler et al 2013;Yu et al 2005). Moreover, well-defined ideal chemical microenvironments and controlled stable spatiotemporal chemical and thermal gradients in microfluidic devices are needed for better understanding of different fundamental processes involved in cell regulating mechanisms and molecular interactions (Nilsson et al 2009;Yew et al 2013).…”
Section: Introductionmentioning
confidence: 97%
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“…Passive microvortices are created by channel geometries like sudden expansions in microscale channels [7,12,15,18,19], cylindrical microcavities [35], trapezoidal side chambers [14], microbifurcations [28], embedded obstacles inside the flow channel [21,36,37], two counterflowing liquid streams [9] or at the boundary layer between sheath and center stream [22].…”
Section: Introductionmentioning
confidence: 99%