Title
Cell responses to electrical pulse stimulation for anticancer drug release
Date Issued
01 August 2019
Access level
open access
Resource Type
journal article
Author(s)
Puiggalí-Jou A.
Alemán C.
Universitat Politècnica de Catalunya
Publisher(s)
Universitat Politècnica de Catalunya
Abstract
Electrical stimulation is an attractive approach to tune on-demand drug release in the body as it relies on simple setups and requires typically 1 V or less. Although many studies have been focused on the development of potential smart materials for electrically controlled drug release, as well as on the exploration of different delivery mechanisms, progress in the field is slow because the response of cells exposed to external electrical stimulus is frequently omitted from such investigations. In this work, we monitor the behavior of prostate and breast cancer cells (PC-3 and MCF7, respectively) exposed to electroactive platforms loaded with curcumin, a hydrophobic anticancer drug. These consist in conducting polymer nanoparticles, which release drug molecules by altering their interactions with polymer, and electrospun polyester microfibres that contain electroactive nanoparticles able to alter the porosity of the matrix through an electro-mechanical actuation mechanism. The response of the cells against different operating conditions has been examined considering their viability, metabolism, spreading and shape. Results have allowed us to differentiate the damage induced in the cell by the electrical stimulation from other effects, as for example, the anticancer activity of curcumin and/or the presence of curcumin-loaded nanoparticles or fibres, demonstrating that these kinds of platforms can be effective when the dosage of the drug occurs under restricted conditions.
Volume
12
Issue
16
Language
English
OCDE Knowledge area
Farmacología, Farmacia Ingeniería química
Scopus EID
2-s2.0-85070969573
Source
Materials
ISSN of the container
19961944
Sponsor(s)
Funding: This research was funded by MINECO, grant numbers RTI2018-098951-B-I00 and RTI2018-101827-B-I00, and by Agència de Gestió d’Ajuts Universitaris i de Recerca, grant numbers 2017SGR359 and 2017SGR373. Acknowledgments: Support for the research of C.A. was received through the prize “ICREA Academia” for excellence in research funded by the Generalitat de Catalunya. Support for the research of C.A. was received through the prize "ICREA Academia" for excellence in research funded by the Generalitat de Catalunya.This research was funded by MINECO, grant numbers RTI2018-098951-B-I00 and RTI2018-101827-B-I00, and by Ag?ncia de Gesti? d'Ajuts Universitaris i de Recerca, grant numbers 2017SGR359 and 2017SGR373
Sources of information: Directorio de Producción Científica Scopus