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dc.contributor.authorRembiałkowska, Nina
dc.contributor.authorNovickij, Vitalij
dc.contributor.authorBaczyńska, Dagmara
dc.contributor.authorDubińska-Magiera, Magda
dc.contributor.authorSaczko, Jolanta
dc.contributor.authorRudno-Rudzińska, Julia
dc.contributor.authorMaciejewska, Magdalena
dc.contributor.authorKulbacka, Julita
dc.date.accessioned2023-09-18T16:18:03Z
dc.date.available2023-09-18T16:18:03Z
dc.date.issued2022
dc.identifier.other(crossref_id)135692671
dc.identifier.urihttps://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.formatPDF
dc.format.extentp. 1-14
dc.format.mediumtekstas / txt
dc.language.isoeng
dc.relation.isreferencedbyScopus
dc.relation.isreferencedbyScience Citation Index Expanded (Web of Science)
dc.rightsLaisvai prieinamas internete
dc.source.urihttps://talpykla.elaba.lt/elaba-fedora/objects/elaba:127167595/datastreams/MAIN/content
dc.titleMicro- and nanosecond pulses used in doxorubicin electrochemotherapy in human breast and colon cancer cells with drug resistance
dc.typeStraipsnis Web of Science DB / Article in Web of Science DB
dcterms.accessRightsThis 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.licenseCreative Commons – Attribution – 4.0 International
dcterms.references37
dc.type.pubtypeS1 - Straipsnis Web of Science DB / Web of Science DB article
dc.contributor.institutionWroclaw Medical University
dc.contributor.institutionVilniaus Gedimino technikos universitetas
dc.contributor.institutionUniversity of Wroclaw
dc.contributor.institutionMedical University Hospital
dc.contributor.institutionHirszfeld Institute of Immunology and Experimental Therapy
dc.contributor.facultyElektronikos fakultetas / Faculty of Electronics
dc.subject.researchfieldT 001 - Elektros ir elektronikos inžinerija / Electrical and electronic engineering
dc.subject.researchfieldN 010 - Biologija / Biology
dc.subject.vgtuprioritizedfieldsMC0505 - Inovatyvios elektroninės sistemos / Innovative Electronic Systems
dc.subject.ltspecializationsL105 - Sveikatos technologijos ir biotechnologijos / Health technologies and biotechnologies
dc.subject.endrug resistance
dc.subject.enhuman adenocarcinoma
dc.subject.endoxorubicin
dc.subject.enelectroporation
dc.subject.endrug delivery
dcterms.sourcetitleMolecules: Electroporation - Drug Delivery and Anticancer Approach
dc.description.issueiss. 7
dc.description.volumevol. 27
dc.publisher.nameMDPI
dc.publisher.cityBasel
dc.identifier.doi135692671
dc.identifier.doi2-s2.0-85127535704
dc.identifier.doi85127535704
dc.identifier.doi1
dc.identifier.doi000781289400001
dc.identifier.doi10.3390/molecules27072052
dc.identifier.elaba127167595


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