Browsing by Author "Rowat, Amy C."
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- Some of the metrics are blocked by yourconsent settingsBiocompatible surfactants for water-in-fluorocarbon emulsions(2008-10-01)
;Holtze, Christian ;Rowat, Amy C. ;Agresti, Jeremy J. ;Hutchison, J. B. ;Angile, Francesco E. ;Schmitz, Christian H. J.; ;Duan, Honey ;Humphry, Katherine J. ;Scanga, R. A. ;Johnson, J. S. ;Pisignano, DarioWeitz, David A.Drops of water-in-fluorocarbon emulsions have great potential for compartmentalizing both in vitro and in vivo biological systems; however, surfactants to stabilize such emulsions are scarce. Here we present a novel class of fluorosurfactants that we synthesize by coupling oligomeric perfluorinated polyethers (PFPE) with polyethyleneglycol (PEG). We demonstrate that these block copolymer surfactants stabilize water-in-fluorocarbon oil emulsions during all necessary steps of a drop-based experiment including drop formation, incubation, and reinjection into a second microfluidic device. Furthermore, we show that aqueous drops stabilized with these surfactants can be used for in vitro translation (IVT), as well as encapsulation and incubation of single cells. The compatability of this emulsion system with both biological systems and polydimethylsiloxane (PDMS) microfluidic devices makes these surfactants ideal for a broad range of high-throughput, drop-based applications. - Some of the metrics are blocked by yourconsent settingsDrop-based microfluidic devices for encapsulation of single cells(2008-05-23)
; ;Angile, Francesco E. ;Duan, Honey ;Agresti, Jeremy J. ;Wintner, Anton ;Schmitz, Christian H. J. ;Rowat, Amy C. ;Merten, Christoph A. ;Pisignano, Dario ;Griffiths, Andrew D.Weitz, David A.We use microfluidic devices to encapsulate, incubate, and manipulate individual cells in picoliter aqueous drops in a carrier fluid at rates of up to several hundred Hz. We use a modular approach with individual devices for each function, thereby significantly increasing the robustness of our system and making it highly flexible and adaptable to a variety of cell-based assays. The small volumes of the drops enables the concentrations of secreted molecules to rapidly attain detectable levels. We show that single hybridoma cells in 33 pL drops secrete detectable concentrations of antibodies in only 6 h and remain fully viable. These devices hold the promise of developing microfluidic cell cytometers and cell sorters with much greater functionality, allowing assays to be performed on individual cells in their own microenvironment prior to analysis and sorting. - Some of the metrics are blocked by yourconsent settingsDropspots(2009-01-07)
;Schmitz, Christian H. J. ;Rowat, Amy C.; Weitz, David A.We present a simple microfluidic device that uses an array of well-defined chambers to immobilize thousands of femtoliter-to picoliter-scale aqueous drops suspended in inert carrier oil. This device enables timelapse studies of large numbers of individual drops, while simultaneously enabling subsequent drop recovery.