Investigation of the mechanisms of action behind Electromotive Drug Administration (EMDA)

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Investigation of the mechanisms of action behind Electromotive Drug Administration (EMDA). / Kos, Bor; Vásquez, Juan Luis; Miklavčĭ, Damijan; Hermann, Gregers G.G.; Gehl, Julie.

I: PeerJ, Bind 2016, Nr. 8, e2309, 2016.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Kos, B, Vásquez, JL, Miklavčĭ, D, Hermann, GGG & Gehl, J 2016, 'Investigation of the mechanisms of action behind Electromotive Drug Administration (EMDA)', PeerJ, bind 2016, nr. 8, e2309. https://doi.org/10.7717/peerj.2309

APA

Kos, B., Vásquez, J. L., Miklavčĭ, D., Hermann, G. G. G., & Gehl, J. (2016). Investigation of the mechanisms of action behind Electromotive Drug Administration (EMDA). PeerJ, 2016(8), [e2309]. https://doi.org/10.7717/peerj.2309

Vancouver

Kos B, Vásquez JL, Miklavčĭ D, Hermann GGG, Gehl J. Investigation of the mechanisms of action behind Electromotive Drug Administration (EMDA). PeerJ. 2016;2016(8). e2309. https://doi.org/10.7717/peerj.2309

Author

Kos, Bor ; Vásquez, Juan Luis ; Miklavčĭ, Damijan ; Hermann, Gregers G.G. ; Gehl, Julie. / Investigation of the mechanisms of action behind Electromotive Drug Administration (EMDA). I: PeerJ. 2016 ; Bind 2016, Nr. 8.

Bibtex

@article{68933e7b2bce451f900e788a972b4235,
title = "Investigation of the mechanisms of action behind Electromotive Drug Administration (EMDA)",
abstract = "Objective. Bladder cancer is a cause of considerable morbidity worldwide. Electromotive Drug Administration is a method that combines intravesical chemotherapy with local electric field application. Electroporation has been suggested among other mechanisms as having a possible role in the therapy, so the goal of the present study was to investigate the electric fields present in the bladder wall during the treatment to determine which mechanisms might be involved. Material and Methods. Electromotive Drug Administration involves applying intravesical mitomycin C with direct current of 20 mA delivered through a catheter electrode for 30 min. For numerical electric field computation we built a 3-D nonhomogeneous patient specific model based on CT images and used finite element method simulations to determine the electric fields in the whole body. Results. Results indicate that highest electric field in the bladder wall was 37.7 V/m. The mean electric field magnitude in the bladder wall was 3.03 V/m. The mean magnitude of the current density in the bladder wall was 0.61 A/m2. Conclusions. The present study shows that electroporation is not the mechanism of action in EMDA. A more likely explanation of the mechanism of action is iontophoretic forces increasing the mitomycin C concentration in the bladder wall.",
keywords = "Bladder cancer, Electromotive drug administration, Electroporation, Mitomycin C",
author = "Bor Kos and V{\'a}squez, {Juan Luis} and Damijan Miklav{\v c}ĭ and Hermann, {Gregers G.G.} and Julie Gehl",
year = "2016",
doi = "10.7717/peerj.2309",
language = "English",
volume = "2016",
journal = "PeerJ",
issn = "2167-8359",
publisher = "PeerJ",
number = "8",

}

RIS

TY - JOUR

T1 - Investigation of the mechanisms of action behind Electromotive Drug Administration (EMDA)

AU - Kos, Bor

AU - Vásquez, Juan Luis

AU - Miklavčĭ, Damijan

AU - Hermann, Gregers G.G.

AU - Gehl, Julie

PY - 2016

Y1 - 2016

N2 - Objective. Bladder cancer is a cause of considerable morbidity worldwide. Electromotive Drug Administration is a method that combines intravesical chemotherapy with local electric field application. Electroporation has been suggested among other mechanisms as having a possible role in the therapy, so the goal of the present study was to investigate the electric fields present in the bladder wall during the treatment to determine which mechanisms might be involved. Material and Methods. Electromotive Drug Administration involves applying intravesical mitomycin C with direct current of 20 mA delivered through a catheter electrode for 30 min. For numerical electric field computation we built a 3-D nonhomogeneous patient specific model based on CT images and used finite element method simulations to determine the electric fields in the whole body. Results. Results indicate that highest electric field in the bladder wall was 37.7 V/m. The mean electric field magnitude in the bladder wall was 3.03 V/m. The mean magnitude of the current density in the bladder wall was 0.61 A/m2. Conclusions. The present study shows that electroporation is not the mechanism of action in EMDA. A more likely explanation of the mechanism of action is iontophoretic forces increasing the mitomycin C concentration in the bladder wall.

AB - Objective. Bladder cancer is a cause of considerable morbidity worldwide. Electromotive Drug Administration is a method that combines intravesical chemotherapy with local electric field application. Electroporation has been suggested among other mechanisms as having a possible role in the therapy, so the goal of the present study was to investigate the electric fields present in the bladder wall during the treatment to determine which mechanisms might be involved. Material and Methods. Electromotive Drug Administration involves applying intravesical mitomycin C with direct current of 20 mA delivered through a catheter electrode for 30 min. For numerical electric field computation we built a 3-D nonhomogeneous patient specific model based on CT images and used finite element method simulations to determine the electric fields in the whole body. Results. Results indicate that highest electric field in the bladder wall was 37.7 V/m. The mean electric field magnitude in the bladder wall was 3.03 V/m. The mean magnitude of the current density in the bladder wall was 0.61 A/m2. Conclusions. The present study shows that electroporation is not the mechanism of action in EMDA. A more likely explanation of the mechanism of action is iontophoretic forces increasing the mitomycin C concentration in the bladder wall.

KW - Bladder cancer

KW - Electromotive drug administration

KW - Electroporation

KW - Mitomycin C

UR - http://www.scopus.com/inward/record.url?scp=84992034662&partnerID=8YFLogxK

U2 - 10.7717/peerj.2309

DO - 10.7717/peerj.2309

M3 - Journal article

AN - SCOPUS:84992034662

VL - 2016

JO - PeerJ

JF - PeerJ

SN - 2167-8359

IS - 8

M1 - e2309

ER -

ID: 318949971