TY - JOUR
T1 - Electrosonic ejector microarray for drug and gene delivery
AU - Zarnitsyn, Vladimir G.
AU - Meacham, J. Mark
AU - Varady, Mark J.
AU - Hao, Chunhai
AU - Degertekin, F. Levent
AU - Fedorov, Andrei G.
N1 - Funding Information:
Acknowledgements We acknowledge Dr. Mark Prausnitz and Dr. Andres Garcia for helpful discussions and access to their lab equipment, Dr. Daniel Hallow for helpful discussions and Dr. Beata Pyrzynska for help with establishing the human malignant glioma cell (cell line LN443) cultures at Georgia Tech. Support for this work by NSF (grant CTS-0323564) and NIH (grant RO1 EB000508-01A1) is also gratefully appreciated.
PY - 2008/4
Y1 - 2008/4
N2 - We report on development and experimental characterization of a novel cell manipulation device-the electrosonic ejector microarray-which establishes a pathway for drug and/or gene delivery with control of biophysical action on the length scale of an individual cell. The device comprises a piezoelectric transducer for ultrasound wave generation, a reservoir for storing the sample mixture and a set of acoustic horn structures that form a nozzle array for focused application of mechanical energy. The nozzles are micromachined in silicon or plastic using simple and economical batch fabrication processes. When the device is driven at a particular resonant frequency of the acoustic horn structures, the sample mixture of cells and desired transfection agents/ molecules suspended in culture medium is ejected from orifices located at the nozzle tips. During sample ejection, focused mechanical forces (pressure and shear) are generated on a microsecond time scale (dictated by nozzle size/geometry and ejection velocity) resulting in identical "active" microenvironments for each ejected cell. This process enables a number of cellular bioeffects, from uptake of small molecules and gene delivery/transfection to cell lysis. Specifically, we demonstrate successful calcein uptake and transfection of DNA plasmid encoding green fluorescent protein (GFP) into human malignant glioma cells (cell line LN443) using electrosonic microarrays with 36, 45 and 50 μm diameter nozzle orifices and operating at ultrasound frequencies between 0.91 and 0.98 MHz. Our results suggest that efficacy and the extent of bioeffects are mainly controlled by nozzle orifice size and the localized intensity of the applied acoustic field.
AB - We report on development and experimental characterization of a novel cell manipulation device-the electrosonic ejector microarray-which establishes a pathway for drug and/or gene delivery with control of biophysical action on the length scale of an individual cell. The device comprises a piezoelectric transducer for ultrasound wave generation, a reservoir for storing the sample mixture and a set of acoustic horn structures that form a nozzle array for focused application of mechanical energy. The nozzles are micromachined in silicon or plastic using simple and economical batch fabrication processes. When the device is driven at a particular resonant frequency of the acoustic horn structures, the sample mixture of cells and desired transfection agents/ molecules suspended in culture medium is ejected from orifices located at the nozzle tips. During sample ejection, focused mechanical forces (pressure and shear) are generated on a microsecond time scale (dictated by nozzle size/geometry and ejection velocity) resulting in identical "active" microenvironments for each ejected cell. This process enables a number of cellular bioeffects, from uptake of small molecules and gene delivery/transfection to cell lysis. Specifically, we demonstrate successful calcein uptake and transfection of DNA plasmid encoding green fluorescent protein (GFP) into human malignant glioma cells (cell line LN443) using electrosonic microarrays with 36, 45 and 50 μm diameter nozzle orifices and operating at ultrasound frequencies between 0.91 and 0.98 MHz. Our results suggest that efficacy and the extent of bioeffects are mainly controlled by nozzle orifice size and the localized intensity of the applied acoustic field.
KW - Biomolecule delivery
KW - Cell manipulation
KW - Electrosonic atomizer
KW - Gene delivery
KW - Microfluidics
UR - https://www.scopus.com/pages/publications/40349114660
U2 - 10.1007/s10544-007-9137-4
DO - 10.1007/s10544-007-9137-4
M3 - Article
C2 - 17994280
AN - SCOPUS:40349114660
SN - 1387-2176
VL - 10
SP - 299
EP - 308
JO - Biomedical Microdevices
JF - Biomedical Microdevices
IS - 2
ER -