dc.contributor.author | Rembiałkowska, Nina | |
dc.contributor.author | Novickij, Vitalij | |
dc.contributor.author | Baczyńska, Dagmara | |
dc.contributor.author | Dubińska-Magiera, Magda | |
dc.contributor.author | Saczko, Jolanta | |
dc.contributor.author | Rudno-Rudzińska, Julia | |
dc.contributor.author | Maciejewska, Magdalena | |
dc.contributor.author | Kulbacka, Julita | |
dc.date.accessioned | 2023-09-18T16:18:03Z | |
dc.date.available | 2023-09-18T16:18:03Z | |
dc.date.issued | 2022 | |
dc.identifier.other | (crossref_id)135692671 | |
dc.identifier.uri | https://etalpykla.vilniustech.lt/handle/123456789/112962 | |
dc.description.abstract | (1) Background: Pulsed electric field (PEF) techniques are commonly used to support the delivery of various molecules. A PEF seems a promising method for low permeability drugs or when cells demonstrate therapy resistance and the cell membrane becomes an impermeable barrier. (2) Methods: In this study, we have used doxorubicin-resistant and sensitive models of human breast cancer (MCF-7/DX, MCF-7/WT) and colon cancer cells (LoVo, LoVoDX). The study aimed to investigate the susceptibility of the cells to doxorubicin (DOX) and electric fields in the 20–900 ns pulse duration range. The viability assay was utilized to evaluate the PEF protocols’ efficacy. Cell confluency and reduced glutathione were measured after PEF protocols. (3) Results: The obtained results showed that PEFs significantly supported doxorubicin delivery and cytotoxicity after 48 and 72 h. The 60 kV/cm ultrashort pulses × 20 ns × 400 had the most significant cytotoxic anticancer effect. The increase in DOX concentration provokes a decrease in cell viability, affected cell confluency, and reduced GSSH when combined with the ESOPE (European Standard Operating Procedures of Electrochemotherapy) protocol. Additionally, reactive oxygen species after PEF and PEF-DOX were detected. (4) Conclusions: Ultrashort electric pulses with low DOX content or ESOPE with higher DOX content seem the most promising in colon and breast cancer treatment. | eng |
dc.format | PDF | |
dc.format.extent | p. 1-14 | |
dc.format.medium | tekstas / txt | |
dc.language.iso | eng | |
dc.relation.isreferencedby | Scopus | |
dc.relation.isreferencedby | Science Citation Index Expanded (Web of Science) | |
dc.rights | Laisvai prieinamas internete | |
dc.source.uri | https://talpykla.elaba.lt/elaba-fedora/objects/elaba:127167595/datastreams/MAIN/content | |
dc.title | Micro- and nanosecond pulses used in doxorubicin electrochemotherapy in human breast and colon cancer cells with drug resistance | |
dc.type | Straipsnis Web of Science DB / Article in Web of Science DB | |
dcterms.accessRights | This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/). | |
dcterms.license | Creative Commons – Attribution – 4.0 International | |
dcterms.references | 37 | |
dc.type.pubtype | S1 - Straipsnis Web of Science DB / Web of Science DB article | |
dc.contributor.institution | Wroclaw Medical University | |
dc.contributor.institution | Vilniaus Gedimino technikos universitetas | |
dc.contributor.institution | University of Wroclaw | |
dc.contributor.institution | Medical University Hospital | |
dc.contributor.institution | Hirszfeld Institute of Immunology and Experimental Therapy | |
dc.contributor.faculty | Elektronikos fakultetas / Faculty of Electronics | |
dc.subject.researchfield | T 001 - Elektros ir elektronikos inžinerija / Electrical and electronic engineering | |
dc.subject.researchfield | N 010 - Biologija / Biology | |
dc.subject.vgtuprioritizedfields | MC0505 - Inovatyvios elektroninės sistemos / Innovative Electronic Systems | |
dc.subject.ltspecializations | L105 - Sveikatos technologijos ir biotechnologijos / Health technologies and biotechnologies | |
dc.subject.en | drug resistance | |
dc.subject.en | human adenocarcinoma | |
dc.subject.en | doxorubicin | |
dc.subject.en | electroporation | |
dc.subject.en | drug delivery | |
dcterms.sourcetitle | Molecules: Electroporation - Drug Delivery and Anticancer Approach | |
dc.description.issue | iss. 7 | |
dc.description.volume | vol. 27 | |
dc.publisher.name | MDPI | |
dc.publisher.city | Basel | |
dc.identifier.doi | 135692671 | |
dc.identifier.doi | 2-s2.0-85127535704 | |
dc.identifier.doi | 85127535704 | |
dc.identifier.doi | 1 | |
dc.identifier.doi | 000781289400001 | |
dc.identifier.doi | 10.3390/molecules27072052 | |
dc.identifier.elaba | 127167595 | |