2000
DOI: 10.1117/12.395646
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<title>Microtools for cell handling</title>

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Cited by 5 publications
(3 citation statements)
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“…These approaches are disadvantageous, especially for valuable or rare samples. It has been widely acknowledged that many microfluidic devices had great potential for single-cell experiments (Telleman et al 2000;Muller et al 2003). Over the years, many methods have been developed, including optical tweezers (Grover et al 2001), optoelectronic tweezers (Ohta et al 2004), micro fluorescence-activated cell sorters (lFACS) (Bonner et al 1972;Fu et al 1999), magnetic-activated cell separation (lMACS) (Telleman et al 1998), microfabricated flow switches (Larsen et al 1996;Lee et al 2001;Huh et al 2001;Tashoro et al 2000), and electrical-fieldbased manipulations and separations (Ichiki et al 2001;Takahashi et al 2004;Schnelle et al 1993;Fuhr et al 1994;Kaler et al 1992;Voldman et al 2003;Pethig 1996;Becker et al 1995;Morgan et al 1999;Hughes 2003;Mü ller et al 1999;Jones and Washizu 1994;Schnelle et al 1999;Fiedler 1998;Dü rr et al 2003;Reichle et al 1999;Schnelle et al 2000;Pohl 1978).…”
Section: Introductionmentioning
confidence: 99%
“…These approaches are disadvantageous, especially for valuable or rare samples. It has been widely acknowledged that many microfluidic devices had great potential for single-cell experiments (Telleman et al 2000;Muller et al 2003). Over the years, many methods have been developed, including optical tweezers (Grover et al 2001), optoelectronic tweezers (Ohta et al 2004), micro fluorescence-activated cell sorters (lFACS) (Bonner et al 1972;Fu et al 1999), magnetic-activated cell separation (lMACS) (Telleman et al 1998), microfabricated flow switches (Larsen et al 1996;Lee et al 2001;Huh et al 2001;Tashoro et al 2000), and electrical-fieldbased manipulations and separations (Ichiki et al 2001;Takahashi et al 2004;Schnelle et al 1993;Fuhr et al 1994;Kaler et al 1992;Voldman et al 2003;Pethig 1996;Becker et al 1995;Morgan et al 1999;Hughes 2003;Mü ller et al 1999;Jones and Washizu 1994;Schnelle et al 1999;Fiedler 1998;Dü rr et al 2003;Reichle et al 1999;Schnelle et al 2000;Pohl 1978).…”
Section: Introductionmentioning
confidence: 99%
“…It has been widely acknowledged that the effective sorting in many microfluidic and lab-on-a-chip devices provide many advantages over the conventional fluorescent activated cell sorting ͑FACS͒, 1 such as low consumption of samples without sacrificing sensitivity, closed system reducing the potential biohazard risks and preventing cross-contamination, and feasibility of making portable and disposable devices. 2 Over the years, scientists have developed many particle and cell handling microfluidic devices-for example, microfabricated fluorescenceactivated cell sorting ͑FACS͒, 3,4 magnetic-activated cell separation ͑MACS͒, 4 automated single-cell sorting using dual-beam optical trapping, 5 optoelectronic tweezers for particle manipulation, 6 and microfabricated flow switches for sample injection and cell/particle sorting. 7,8 Air-liquid two-phase 9 and three-dimensional ͑3-D͒ sheath flow-type 10 microchannels are also reported.…”
Section: Introductionmentioning
confidence: 99%
“…It has been widely acknowledged that the effective sorting in many micro-fluidic and Lab-On-A-Chip devices provided many advantages over the conventional fluorescent activated cell sorting (FACS) [1], such as low consumption of samples without sacrificing sensitivity, closed system reducing the potential biohazard risks and preventing cross-contamination, and feasibility of making portable and disposable devices [2]. Over the years, the scientists have developed many particle and cell handling microfluidic devices.…”
Section: Introductionmentioning
confidence: 99%