Transdermal transport pathway creation: electroporation pulse order
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Publication:472780
DOI10.1016/J.MBS.2014.07.001zbMATH Open1370.92021OpenAlexW2109261849WikidataQ51067926 ScholiaQ51067926MaRDI QIDQ472780FDOQ472780
Authors: Sid Becker, Barbara Zorec, Damijan Miklavčič, Nataša Pavšelj 
Publication date: 20 November 2014
Published in: Mathematical Biosciences (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1016/j.mbs.2014.07.001
Recommendations
- Thermal in vivo skin electroporation pore development and charged macromolecule transdermal delivery: A numerical study of the influence of chemically enhanced lower lipid phase transition temperatures
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- Iontophoretic transdermal drug delivery: a multi-layered approach
- Resistive heating and electropermeabilization of skin tissue during in vivo electroporation: a coupled nonlinear finite element model
- Electrophoretic transport through channels of periodically varying cross section
Cites Work
- Thermal in vivo skin electroporation pore development and charged macromolecule transdermal delivery: A numerical study of the influence of chemically enhanced lower lipid phase transition temperatures
- Resistive heating and electropermeabilization of skin tissue during in vivo electroporation: a coupled nonlinear finite element model
Cited In (7)
- Coupling nonlinear electric fields and temperature to enhance drug transport: an accurate numerical tool
- Thermal damage reduction associated with in vivo skin electroporation: a numerical investigation justifying aggressive pre-cooling
- Resistive heating and electropermeabilization of skin tissue during in vivo electroporation: a coupled nonlinear finite element model
- Second order approximations for kinetic and potential energies in Maxwell's wave equations
- Transdermal iontophoresis -- a quantitative and qualitative study
- Aging Effect on Iontophoretic Transdermal Drug Delivery
- Thermal in vivo skin electroporation pore development and charged macromolecule transdermal delivery: A numerical study of the influence of chemically enhanced lower lipid phase transition temperatures
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