From Droplets to Cells: Physics, Devices and Applications

Meacham, J. Mark

Title:

From Droplets to Cells: Physics, Devices and Applications

dc.contributor.author	Meacham, J. Mark
dc.contributor.corporatename	OpenCell Technologies
dc.date.accessioned	2010-11-22T22:07:01Z
dc.date.available	2010-11-22T22:07:01Z
dc.date.issued	2010-11-09
dc.description	J. Mark Meacham, CEO at OpenCell Technologies presented a lecture at the Nano@Tech Meeting on November 9, 2010 at 12 noon in room 1116 of the Marcus Nanotechnology Building.	en_US
dc.description	Runtime: 56:26 minutes
dc.description	J. Mark Meacham received his B.S. and M.S. degrees in mechanical engineering from Iowa State University, Ames, IA, in 1999 and 2002, respectively. He received his Ph.D. in mechanical engineering from the Georgia Institute of Technology, Atlanta, GA, in 2006, where he investigated the physics of droplet ejection from a novel ultrasonic atomizer. In 2006, he received an NRC postdoctoral research fellowship to investigate improved microfluidics-based technologies for counterflow separations in the Biochemical Sciences division at NIST. His research interests include microfluidics and MEMS, with application to development of biomedical devices and life sciences tools.
dc.description.abstract	The ability to introduce drugs, genes, nucleic acids, and/or imaging agents into living cells is critical to drug design and delivery, as well as to many cell biology and genetic modification protocols. However, intracellular delivery and transfection remain difficult tasks. Through synergetic use of focused physical fields (e.g., fluidic, acoustic, electric, thermal and solutal), micro-fabricated devices can enable localized control of the extracellular environment leading to desired bioeffects. Conception, analysis and demonstration of one such device are presented. The Electrosonic Actuation Microarray is a novel microelectromechanical systems (MEMS)-enabled device that ejects sample containing biological cells through microscopic (of order size of a single cell) nozzles with incorporated electroporation electrodes. Focused mechanical (pressure and shear) and electrical forces are generated on a microsecond time scale-dictated by nozzle geometry, ejection frequency and velocity, and electroporation voltage. This yields identical "active" microenvironments for each ejected cell. Technical details of device operation and the physics describing droplet formation and ejection are included. The ejection process enables a number of cellular bioeffects, from uptake of small molecules to gene delivery and transfection. Specifically, we demonstrate calcein uptake and transfection of DNA plasmid encoding green fluorescent protein (GFP) into human malignant glioma and human embryonic kidney cells using microarrays with 30 to 55 μm diameter nozzle orifices and operating at ultrasound frequencies between 0.90 and 1.4 MHz. Typical electroporation field strengths are 0.4-1.7 kV/cm.	en_US
dc.format.extent	56:26 minutes
dc.identifier.uri	http://hdl.handle.net/1853/36087
dc.language.iso	en_US	en_US
dc.publisher	Georgia Institute of Technology	en_US
dc.relation.ispartofseries	Nano@Tech Lecture Series
dc.subject	Intracellular delivery	en_US
dc.subject	Microelectromechanical systems	en_US
dc.subject	Nanotechnology	en_US
dc.subject	Transfection	en_US
dc.title	From Droplets to Cells: Physics, Devices and Applications	en_US
dc.type	Moving Image
dc.type.genre	Lecture
dspace.entity.type	Publication
local.contributor.corporatename	Institute for Electronics and Nanotechnology (IEN)
local.relation.ispartofseries	Nano@Tech Lecture Series
relation.isOrgUnitOfPublication	5d316582-08fe-42e1-82e3-9f3b79dd6dae
relation.isSeriesOfPublication	accfbba8-246e-4389-8087-f838de8956cf