Continuous electrochemical H2O2 delivery for cancer cell treatment

dc.contributor.authorJakešová, Mariecs
dc.contributor.authorEhlich, Jiřícs
dc.contributor.authorErschen, Sabinecs
dc.contributor.authorNemeskeri, Leiacs
dc.contributor.authorHandl, Verenacs
dc.contributor.authorWaldherr, Lindacs
dc.contributor.authorGlowacki, Eric Danielcs
dc.coverage.issue3cs
dc.coverage.volume14cs
dc.date.accessioned2026-02-05T03:53:34Z
dc.date.issued2026-01-21cs
dc.description.abstractHydrogen peroxide (H2O2) has emerged as a promising agent in cancer therapy due to its ability to induce oxidative stress selectively in tumor cells, however, its efficacy is severely hampered by H2O2 breakdown when administered via standard routes. Our study introduces an innovative electrochemical method for the controlled and continuous delivery of H2O2 directly to cancer cells, potentially enhancing the efficacy of cancer treatments. We investigated the performance of gold, titanium, stainless steel, and poly(3,4-ethylenedioxythiophene), PEDOT, electrodes in generating H2O2, with PEDOT exhibiting superior consistency and efficiency in cell culture medium. The galvanostatic delivery of H2O2 demonstrated a dose-dependent reduction in cell viability for U87 glioblastoma and A375 melanoma cells, confirming the cytotoxic impact of H2O2. The addition of catalase restored cell viability, further validating the specificity of H2O2-induced cell death. Our results showed that U87 cells exhibited higher resistance to H2O2 compared to A375 cells, aligning with known tumor-specific variations in H2O2 metabolism. This novel approach of electrochemical H2O2 delivery holds significant potential for enhancing targeted cancer therapies, offering a controllable, precise, and efficient method for inducing tumor cell death while minimizing damage to healthy tissues. These results showcase the remarkable ability of PEDOT electrodes as a reliable electrocatalytic source of on-demand H2O2 in electrochemically-challenging biological environments.en
dc.description.abstractHydrogen peroxide (H2O2) has emerged as a promising agent in cancer therapy due to its ability to induce oxidative stress selectively in tumor cells, however, its efficacy is severely hampered by H2O2 breakdown when administered via standard routes. Our study introduces an innovative electrochemical method for the controlled and continuous delivery of H2O2 directly to cancer cells, potentially enhancing the efficacy of cancer treatments. We investigated the performance of gold, titanium, stainless steel, and poly(3,4-ethylenedioxythiophene), PEDOT, electrodes in generating H2O2, with PEDOT exhibiting superior consistency and efficiency in cell culture medium. The galvanostatic delivery of H2O2 demonstrated a dose-dependent reduction in cell viability for U87 glioblastoma and A375 melanoma cells, confirming the cytotoxic impact of H2O2. The addition of catalase restored cell viability, further validating the specificity of H2O2-induced cell death. Our results showed that U87 cells exhibited higher resistance to H2O2 compared to A375 cells, aligning with known tumor-specific variations in H2O2 metabolism. This novel approach of electrochemical H2O2 delivery holds significant potential for enhancing targeted cancer therapies, offering a controllable, precise, and efficient method for inducing tumor cell death while minimizing damage to healthy tissues. These results showcase the remarkable ability of PEDOT electrodes as a reliable electrocatalytic source of on-demand H2O2 in electrochemically-challenging biological environments.en
dc.formattextcs
dc.format.extent894-902cs
dc.format.mimetypeapplication/pdfcs
dc.identifier.citationJournal of Materials Chemistry B. 2026, vol. 14, issue 3, p. 894-902.en
dc.identifier.doi10.1039/d5tb01244acs
dc.identifier.issn2050-750Xcs
dc.identifier.orcid0000-0002-8702-2303cs
dc.identifier.orcid0000-0003-0478-6875cs
dc.identifier.orcid0009-0009-8783-1424cs
dc.identifier.orcid0000-0001-9817-1358cs
dc.identifier.orcid0000-0002-0280-8017cs
dc.identifier.other200771cs
dc.identifier.researcheridHGB-6954-2022cs
dc.identifier.researcheridCNO-1022-2022cs
dc.identifier.researcheridNUK-8296-2025cs
dc.identifier.researcheridHJJ-1365-2023cs
dc.identifier.researcheridABD-4869-2021cs
dc.identifier.urihttps://hdl.handle.net/11012/256039
dc.language.isoencs
dc.relation.ispartofJournal of Materials Chemistry Bcs
dc.relation.urihttps://pubs.rsc.org/en/content/articlelanding/2026/tb/d5tb01244acs
dc.rightsCreative Commons Attribution 3.0 Unportedcs
dc.rights.accessopenAccesscs
dc.rights.sherpahttp://www.sherpa.ac.uk/romeo/issn/2050-750X/cs
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/cs
dc.subjecthydrogen-peroxide; oxygen reduction reactionen
dc.subjectoxidative stressen
dc.subjecthydrogen-peroxide; oxygen reduction reaction
dc.subjectoxidative stress
dc.titleContinuous electrochemical H2O2 delivery for cancer cell treatmenten
dc.title.alternativeContinuous electrochemical H2O2 delivery for cancer cell treatmenten
dc.type.driverarticleen
dc.type.statusPeer-revieweden
dc.type.versionpublishedVersionen
eprints.grantNumberinfo:eu-repo/grantAgreement/GA0/GA/GA23-07432Scs
sync.item.dbidVAV-200771en
sync.item.dbtypeVAVen
sync.item.insts2026.02.05 04:53:34en
sync.item.modts2026.02.05 04:32:13en
thesis.grantorVysoké učení technické v Brně. Středoevropský technologický institut VUT. Bioelektronické materiály a systémycs

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