Title :
A Rapid Microfluidic Switching System for Analysis at the Single Cellular Level
Author :
Yamada, Akira ; Katanosaka, Yuki ; Mohri, Satoshi ; Naruse, Keiji
Author_Institution :
Cardiovascular Physiol., Okayama Univ., Okayama, Japan
Abstract :
Analysis of cellular responses to chemicals at high spatiotemporal resolution is required for precise understanding of intracellular signal transduction. Here, we demonstrated a novel method for applying different solutions to a part of or all of a cell at high spatiotemporal resolution. We fabricated a microfluidic device using polydimethylsiloxane, and the sharp interface between the two solution streams flowing in the channel was used for the application of different solutions. We constructed a computer-controlled system to control the interface movement precisely, rapidly, and reproducibly during positioning, and spatial and temporal resolutions attained were 1.6 ¿m and 189 ms, respectively. We then applied the present system to the analysis of intracellular responses to chemicals. We were able to measure [Ca2+]i increases within 500 ms, when one laminar stream covered a part of the cell. This method can be used as a generic platform to investigate responses against drugs at the single cell level.
Keywords :
bioMEMS; bioelectric phenomena; biomembrane transport; calcium; laminar flow; microfluidics; microswitches; Ca; interface movement; intracellular signal transduction; microfluidic switch; polydimethylsiloxane; single cellular level; time 189 mus; Application software; Chemical analysis; Computer interfaces; Control systems; Microfluidics; Signal analysis; Signal resolution; Spatial resolution; Spatiotemporal phenomena; Switching systems; Adherent; adenosine 5’-triphosphate (ATP); human embryonic kidney 293 (HEK 293); laminar flow; microfluidic device; perfusion; polydimethylsiloxane (PDMS); single cell; Adenosine Triphosphate; Biomedical Engineering; Calcium Signaling; Cell Line; Equipment Design; Humans; Microfluidic Analytical Techniques; Perfusion;
Journal_Title :
NanoBioscience, IEEE Transactions on
DOI :
10.1109/TNB.2009.2035253