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Doxorubicin Delivery into Tumor Cells by Stable Cavitation without Contrast Agents

Authors :
Maxime Lafond
Cyril Lafon
Kamel Chettab
Charles Dumontet
Jean-Louis Mestas
Djamel Eddine Saadna
Centre de Psychiatrie et Neurosciences ( CPN - U894 )
Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Université Paris Descartes - Paris 5 ( UPD5 )
Application des ultrasons à la thérapie ( LabTAU )
Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 ( UCBL )
Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale ( INSERM )
Equipe 14
Centre de Recherche en Cancérologie de Lyon ( CRCL )
Université Claude Bernard Lyon 1 ( UCBL )
Université de Lyon-Université de Lyon-Centre Léon Bérard [Lyon]-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS ) -Université Claude Bernard Lyon 1 ( UCBL )
Université de Lyon-Université de Lyon-Centre Léon Bérard [Lyon]-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS )
Université Paris Descartes - Paris 5 ( UPD5 ) -Institut National de la Santé et de la Recherche Médicale ( INSERM )
Source :
Molecular Pharmaceutics, Molecular Pharmaceutics, American Chemical Society, 2017, 14 (2), pp.441-447
Publication Year :
2017
Publisher :
American Chemical Society (ACS), 2017.

Abstract

International audience; Doxorubicin, alone or in combination with other anticancer agents, is one of the most widely used chemotherapeutic agents and is administered in a wide range of cancers. However, the use of doxorubicin is limited due to its potential serious adverse reactions. Previous studies have established the ability of high intensity focused ultrasound (HIFU) in combination with various contrast agents to increase intracellular doxorubicin delivery in a targeted and noninvasive manner. In this study, we developed a new sonoporation device generating and monitoring acoustic cavitation bubbles without any addition of contrast agents. The device was used to potentiate the delivery of active doxorubicin into both adherent and suspended cell lines. Combining doxorubicin with ultrasound resulted in a significant enhancement of doxorubicin intracellular delivery and a decrease in cell viability at 48 and 72 h, in comparison to doxorubicin alone. More importantly and unlike previous investigations, our procedure does not require the addition of contrast agents to generate acoustic cavitation and to achieve high levels of doxorubicin delivery. The successful translation of this approach for an in vivo application may allow a significant reduction in the dosage and the adverse effects of doxorubicin therapy in patients.

Details

ISSN :
15438392 and 15438384
Volume :
14
Database :
OpenAIRE
Journal :
Molecular Pharmaceutics
Accession number :
edsair.doi.dedup.....9f2669e1d870fb950926635ee5fd4367
Full Text :
https://doi.org/10.1021/acs.molpharmaceut.6b00880