Low-frequency ac electroporation shows strong frequency dependence and yields comparable transfection results to dc electroporation.

Conventional electroporation has been conducted by employing short direct current (dc) pulses for delivery of macromolecules such as DNA into cells. The use of alternating current (ac) field for electroporation has mostly been explored in the frequency range of 10kHz-1MHz. Based on Schwan equation, it was thought that with low ac frequencies (10Hz-10kHz), the transmembrane potential does not vary with the frequency. In this report, we utilized a flow-through electroporation technique that employed continuous 10Hz-10kHz ac field (based on either sine waves or square waves) for electroporation of cells with defined duration and intensity. Our results reveal that electropermeabilization becomes weaker with increased frequency in this range. In contrast, transfection efficiency with DNA reaches its maximum at medium frequencies (100-1000Hz) in the range. We postulate that the relationship between the transfection efficiency and the ac frequency is determined by combined effects from electrophoretic movement of DNA in the ac field, dependence of the DNA/membrane interaction on the ac frequency, and variation of transfection under different electropermeabilization intensities. The fact that ac electroporation in this frequency range yields high efficiency for transfection (up to ~71% for Chinese hamster ovary cells) and permeabilization suggests its potential for gene delivery.

[1]  A. van den Berg,et al.  Gene transfer and protein dynamics in stem cells using single cell electroporation in a microfluidic device. , 2008, Lab on a chip.

[2]  H P Schwan,et al.  Cellular membrane potentials induced by alternating fields. , 1992, Biophysical journal.

[3]  Marie-Pierre Rols,et al.  What is (Still not) Known of the Mechanism by Which Electroporation Mediates Gene Transfer and Expression in Cells and Tissues , 2009, Molecular biotechnology.

[4]  J. Weaver,et al.  Electroporation of mammalian skin: a mechanism to enhance transdermal drug delivery. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[5]  Brian E. Henslee,et al.  Gene transfection of mammalian cells using membrane sandwich electroporation. , 2007, Analytical chemistry.

[6]  D. Chang,et al.  High efficiency gene transfection by electroporation using a radio-frequency electric field. , 1991, Biochimica et biophysica acta.

[7]  E. Tekle,et al.  Electroporation by using bipolar oscillating electric field: an improved method for DNA transfection of NIH 3T3 cells. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Chang Lu,et al.  Electroporation of mammalian cells in a microfluidic channel with geometric variation. , 2006, Analytical chemistry.

[9]  Weixiong Wang,et al.  Semicontinuous flow electroporation chip for high-throughput transfection on mammalian cells. , 2009, Analytical chemistry.

[10]  E. Stellwagen,et al.  Determining the electrophoretic mobility and translational diffusion coefficients of DNA molecules in free solution , 2002, Electrophoresis.

[11]  Y. Tai,et al.  A micro cell lysis device , 1999 .

[12]  D Miklavcic,et al.  The influence of medium conductivity on electropermeabilization and survival of cells in vitro. , 2001, Bioelectrochemistry.

[13]  J. Weaver,et al.  Theory of electroporation: A review , 1996 .

[14]  M. Rols,et al.  In vivo electrically mediated protein and gene transfer in murine melanoma , 1998, Nature Biotechnology.

[15]  J Teissié,et al.  In vitro and in vivo electric field-mediated permeabilization, gene transfer, and expression. , 2004, Methods.

[16]  Yong Huang,et al.  Flow-through micro-electroporation chip for high efficiency single-cell genetic manipulation , 2003 .

[17]  Mark Bachman,et al.  Fast-lysis cell traps for chemical cytometry. , 2008, Lab on a chip.

[18]  H. Aihara,et al.  Gene transfer into muscle by electroporation in vivo. , 1998, Nature biotechnology.

[19]  Mojca Pavlin,et al.  Electro‐mediated gene transfer and expression are controlled by the life‐time of DNA/membrane complex formation , 2010, The journal of gene medicine.

[20]  D. Chang,et al.  Cell poration and cell fusion using an oscillating electric field. , 1989, Biophysical journal.

[21]  Luke P. Lee,et al.  Single-cell electroporation arrays with real-time monitoring and feedback control. , 2007, Lab on a chip.

[22]  J Teissié,et al.  Electropermeabilization of mammalian cells. Quantitative analysis of the phenomenon. , 1990, Biophysical journal.

[23]  Hsan-Yin Hsu,et al.  Parallel single-cell light-induced electroporation and dielectrophoretic manipulation. , 2009, Lab on a chip.

[24]  L. Mir,et al.  Mechanisms of in vivo DNA electrotransfer: respective contributions of cell electropermeabilization and DNA electrophoresis. , 2002, Molecular therapy : the journal of the American Society of Gene Therapy.

[25]  Boris Rubinsky,et al.  Micro-electroporation of mesenchymal stem cells with alternating electrical current pulses , 2009, Biomedical microdevices.

[26]  S W Smye,et al.  Measurement of the efficiency of cell membrane electroporation using pulsed ac fields , 2008, Physics in medicine and biology.

[27]  R. Jaenisch,et al.  Microfluidic Control of Cell Pairing and Fusion , 2009, Nature Methods.

[28]  T. Geng,et al.  Transfection of cells using flow-through electroporation based on constant voltage , 2011, Nature Protocols.

[29]  K. Jensen,et al.  A microfluidic electroporation device for cell lysis. , 2005, Lab on a chip.

[30]  O. Orwar,et al.  Control of the release of freely diffusing molecules in single-cell electroporation. , 2009, Analytical chemistry.

[31]  M. Rols,et al.  Direct visualization at the single-cell level of electrically mediated gene delivery , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[32]  Y. Zhan,et al.  Vortex-assisted DNA delivery. , 2010, Lab on a chip.

[33]  T. Tsong,et al.  Schwan equation and transmembrane potential induced by alternating electric field. , 1990, Biophysical journal.

[34]  H. Petty,et al.  Alterations of the electrophoretic mobility distribution of rat mast cells after immunologic activation. , 1980, Biophysical journal.

[35]  G. G. Stokes "J." , 1890, The New Yale Book of Quotations.

[36]  Luke P. Lee,et al.  A single cell electroporation chip. , 2005, Lab on a chip.

[37]  Bo Yu,et al.  Nanochannel electroporation delivers precise amounts of biomolecules into living cells. , 2011, Nature nanotechnology.

[38]  Chang Lu,et al.  Microfluidic electroporation for delivery of small molecules and genes into cells using a common DC power supply , 2008, Biotechnology and bioengineering.

[39]  Chang Lu,et al.  High‐throughput and real‐time study of single cell electroporation using microfluidics: Effects of medium osmolarity , 2006, Biotechnology and bioengineering.

[40]  J Teissié,et al.  Control by osmotic pressure of voltage-induced permeabilization and gene transfer in mammalian cells. , 1998, Biophysical journal.

[41]  Damijan Miklavcic,et al.  Second-order model of membrane electric field induced by alternating external electric fields , 2000, IEEE Transactions on Biomedical Engineering.

[42]  T. Geng,et al.  Flow-through electroporation based on constant voltage for large-volume transfection of cells. , 2010, Journal of controlled release : official journal of the Controlled Release Society.

[43]  E Neumann,et al.  Control by pulse parameters of electric field-mediated gene transfer in mammalian cells. , 1994, Biophysical journal.

[44]  Chang Lu,et al.  Microfluidic electroporation of tumor and blood cells: observation of nucleus expansion and implications on selective analysis and purging of circulating tumor cells. , 2010, Integrative biology : quantitative biosciences from nano to macro.

[45]  L. Mir,et al.  Electrophoretic component of electric pulses determines the efficacy of in vivo DNA electrotransfer. , 2005, Human gene therapy.

[46]  J. R. Claycomb,et al.  Effects of oscillatory electric fields on internal membranes: an analytical model. , 2008, Biophysical journal.

[47]  E. Neumann,et al.  Gene transfer into mouse lyoma cells by electroporation in high electric fields. , 1982, The EMBO journal.

[48]  M. Rols,et al.  Mechanisms of cell membrane electropermeabilization: a minireview of our present (lack of ?) knowledge. , 2005, Biochimica et biophysica acta.

[49]  Yu-Cheng Lin,et al.  Simulation and experimental demonstration of the electric field assisted electroporation microchip for in vitro gene delivery enhancement. , 2004, Lab on a chip.