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Excitation and electroporation by MHz bursts of nanosecond stimuli.
Pakhomov, Andrei G; Xiao, Shu; Novickij, Vitalij; Casciola, Maura; Semenov, Iurii; Mangalanathan, Uma; Kim, Vitalii; Zemlin, Christian; Sozer, Esin; Muratori, Claudia; Pakhomova, Olga N.
Afiliação
  • Pakhomov AG; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA. Electronic address: andrei@pakhomov.net.
  • Xiao S; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA; Department of Electrical and Computer Engineering, Old Dominion University, Norfolk, VA, USA.
  • Novickij V; Vilnius Gediminas Technical University, Vilnius, Lithuania.
  • Casciola M; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA.
  • Semenov I; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA.
  • Mangalanathan U; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA.
  • Kim V; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA.
  • Zemlin C; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA; Department of Electrical and Computer Engineering, Old Dominion University, Norfolk, VA, USA.
  • Sozer E; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA.
  • Muratori C; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA.
  • Pakhomova ON; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA.
Biochem Biophys Res Commun ; 518(4): 759-764, 2019 10 22.
Article em En | MEDLINE | ID: mdl-31472962
Intense nanosecond pulsed electric field (nsPEF) is a novel modality for cell activation and nanoelectroporation. Applications of nsPEF in research and therapy are hindered by a high electric field requirement, typically from 1 to over 50 kV/cm to elicit any bioeffects. We show how this requirement can be overcome by engaging temporal summation when pulses are compressed into high-rate bursts (up to several MHz). This approach was tested for excitation of ventricular cardiomyocytes and peripheral nerve fibers; for membrane electroporation of cardiomyocytes, CHO, and HEK cells; and for killing EL-4 cells. MHz compression of nsPEF bursts (100-1000 pulses) enables excitation at only 0.01-0.15 kV/cm and electroporation already at 0.4-0.6 kV/cm. Clear separation of excitation and electroporation thresholds allows for multiple excitation cycles without membrane disruption. The efficiency of nsPEF bursts increases with the duty cycle (by increasing either pulse duration or repetition rate) and with increasing the total time "on" (by increasing either pulse duration or number). For some endpoints, the efficiency of nsPEF bursts matches a single "long" pulse whose amplitude and duration equal the time-average amplitude and duration of the bursts. For other endpoints this rule is not valid, presumably because of nsPEF-specific bioeffects and/or possible modification of targets already during the burst. MHz compression of nsPEF bursts is a universal and efficient way to lower excitation thresholds and facilitate electroporation.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Potenciais de Ação / Permeabilidade da Membrana Celular / Eletroporação / Miócitos Cardíacos / Fibras Nervosas Limite: Animals / Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Potenciais de Ação / Permeabilidade da Membrana Celular / Eletroporação / Miócitos Cardíacos / Fibras Nervosas Limite: Animals / Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2019 Tipo de documento: Article