Red haloBODIPYs as theragnostic agents: The role of the substitution at meso position
dc.contributor.author | Prieto Montero, Ruth | |
dc.contributor.author | Prieto Castañeda, Alejandro | |
dc.contributor.author | Katsumiti, Alberto | |
dc.contributor.author | Sola Llano, Rebeca | |
dc.contributor.author | Rodríguez Agarrabeitia, Antonia | |
dc.contributor.author | Cajaraville, Miren P. | |
dc.contributor.author | Ortiz García, María Josefa | |
dc.contributor.author | Martínez Martínez, Virginia | |
dc.date | Received 31 July 2021; Received in revised form 2 November 2021; Accepted 3 December 2021 | |
dc.date.accessioned | 2023-06-16T14:18:21Z | |
dc.date.available | 2023-06-16T14:18:21Z | |
dc.date.issued | 2021-12-04 | |
dc.description.abstract | Three different molecular designs based on BODIPY dye have been proposed as photosensitizers (PSs) for photodynamic therapy (PDT) by the inclusion of halogen atoms (Iodine) at 2,6-positions and with extended conjugation at 3, 5-positions and varying the substitution at meso position. The synthesis is described and their main photophysical features including singlet oxygen production and triplet states were characterized by absorption and fluorescence spectroscopy (steady-state and time-correlated) and nanosecond transient absorption spectroscopy. The results were compared with the commercial Chlorin e6. The three new red-halogen-BODIPYs showed a great balance between singlet oxygen generation (ΦΔ≥0.40) and fluorescence (Φfl≥0.22) for potential application on PDT, and particularly in theragnosis. In vitro experiments in HeLa cells were done to study their performance and to elucidate the best potential candidate for PDT. | en |
dc.description.department | Sección Deptal. de Química Orgánica (Óptica y Optometría) | |
dc.description.faculty | Fac. de Óptica y Optometría | |
dc.description.refereed | TRUE | |
dc.description.sponsorship | Ministerio de Ciencia, Innovación y Universidades (España) | |
dc.description.sponsorship | Gobierno Vasco | |
dc.description.sponsorship | Universidad del País Vasco | |
dc.description.status | pub | |
dc.eprint.id | https://eprints.ucm.es/id/eprint/69355 | |
dc.identifier.citation | Prieto Montero, R., Prieto Castañeda, A., Katsumiti, A. et al. «Red haloBODIPYs as Theragnostic Agents: The Role of the Substitution at Meso Position». Dyes and Pigments, vol. 198, febrero de 2022, p. 110015. DOI.org (Crossref), https://doi.org/10.1016/j.dyepig.2021.110015. | |
dc.identifier.doi | 10.1016/j.dyepig.2021.110015 | |
dc.identifier.issn | 0143-7208 | |
dc.identifier.officialurl | https://doi.org/10.1016/j.dyepig.2021.110015 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14352/4603 | |
dc.journal.title | Dyes and Pigments | |
dc.language.iso | eng | |
dc.page.initial | 10 p. | |
dc.publisher | Elsevier | |
dc.relation.projectID | MAT(2017-83856-C3-2-P y 3-P), PID(2020-114347RB-C32), PID(2020-114755 GB-C32) | |
dc.relation.projectID | IT(912-16), IT(-1302-19) y IT(1639-22) | |
dc.relation.projectID | COLAB(19 / 01.) | |
dc.rights | Atribución-NoComercial-SinDerivadas 3.0 España | |
dc.rights.accessRights | open access | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/3.0/es/ | |
dc.subject.cdu | 547.1:615.8 | |
dc.subject.cdu | 543.426 | |
dc.subject.cdu | 615.8 | |
dc.subject.keyword | BODIPY photosensitizer | |
dc.subject.keyword | Singlet oxygen | |
dc.subject.keyword | Photodynamic therapy | |
dc.subject.keyword | HeLa cells | |
dc.subject.keyword | Theragnosis | |
dc.subject.ucm | Química física (Física) | |
dc.subject.ucm | Química orgánica (Química) | |
dc.subject.unesco | 2210 Química Física | |
dc.subject.unesco | 2306 Química Orgánica | |
dc.title | Red haloBODIPYs as theragnostic agents: The role of the substitution at meso position | en |
dc.type | journal article | |
dc.volume.number | 198 | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | bee889c2-938d-48d9-8748-01e3c8bf5614 | |
relation.isAuthorOfPublication | 0486160c-3df6-4270-bf91-3e96cd33d85d | |
relation.isAuthorOfPublication | 07f337af-8a30-4929-81db-4e92176e5c87 | |
relation.isAuthorOfPublication.latestForDiscovery | bee889c2-938d-48d9-8748-01e3c8bf5614 |
Download
Original bundle
1 - 1 of 1
Loading...
- Name:
- 1-s2.0-S0143720821008810-main.pdf
- Size:
- 2.15 MB
- Format:
- Adobe Portable Document Format