2007
DOI: 10.1088/1464-4258/9/8/s02
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Optical manipulation and microfluidics for studies of single cell dynamics

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Cited by 52 publications
(36 citation statements)
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“…It was found that there was no contamination when cells were dragged to a place with a different liquid medium and then transferred back again from different channels. This group (Eriksson et al 2007) used this technique to investigate the cell response to a sharp glucose concentration gradient between the two channels in which 25 yeast cells were moved back and forth between the two media by holographic OT. This provides a new method to investigate real-time cell responses to various extracellular environment conditions without being removed from the field of view of the microscope.…”
Section: Active Nanomanipulationmentioning
confidence: 99%
“…It was found that there was no contamination when cells were dragged to a place with a different liquid medium and then transferred back again from different channels. This group (Eriksson et al 2007) used this technique to investigate the cell response to a sharp glucose concentration gradient between the two channels in which 25 yeast cells were moved back and forth between the two media by holographic OT. This provides a new method to investigate real-time cell responses to various extracellular environment conditions without being removed from the field of view of the microscope.…”
Section: Active Nanomanipulationmentioning
confidence: 99%
“…Several other methods have also been coupled with microfluidics for cell immobilization and conducting controlled, complete cell assays. Flow-based active cell trapping by using control valves [14,15], non-invasive optical trapping [16][17][18], dielectrophoresis [19][20][21], surface chemistry modification techniques [22,23], arrays of physical barriers [24], cell trapping by negative pressure [25,26], and hydrodynamic methods [27][28][29] are some of these successfully established techniques.…”
Section: Introductionmentioning
confidence: 99%
“…In our previous work, we developed an experimental platform combining a microfluidic chamber with optical tweezers and advanced time-lapse microscopy [17,30,31], which has vastly been used to identify the underlying mechanisms of different signaling pathways in Saccharomyces cerevisiae (budding yeast) cells. Cells were trapped by the optical tweezers and positioned precisely in an array format at the bottom of the microfluidic chamber.…”
Section: Introductionmentioning
confidence: 99%
“…To this end, RT have been combined with microfluidic systems that allow fast, controlled exchange of the microliter volumes of working fluids in the sample chamber, injection and collection of the analyzed specimen through multiple inlet/outlet ports, and incorporation of various optical sorting techniques [431,432] (see Section 4.6). Such a combination of RT with a microfluidic system was employed by Ramser et al to study the oxygenation cycle in single optically trapped red blood cells [433,434]. The transition between the oxygenated and de-oxygenated hemoglobin states was triggered by flushing the working channel with the solution of sodium dithionite in HEPES buffer via electro-osmotic flow.…”
mentioning
confidence: 99%