IN VITRO PHOTODYNAMIC THERAPY ON OCULAR MELANOMA CELLS

dc.contributor.authorGuimarães, Tarcísio Guerra
dc.contributor.authorCarvalho, Gabriela
dc.contributor.authorMamede, Fabrício Vilela
dc.contributor.authorCardoso, Karla Menezes
dc.contributor.authorMarto, Carlos Miguel
dc.contributor.authorPiñeiro, Marta
dc.contributor.authorPinho e Melo, Teresa
dc.contributor.authorAlexandre, Nuno
dc.contributor.authorBotelho, Maria Filomena
dc.contributor.authorLaranjo, Mafalda
dc.date.accessioned2023-02-16T16:45:53Z
dc.date.available2023-02-16T16:45:53Z
dc.date.issued2022-10-27
dc.description.abstractPurpose. To evaluate the effect of newly developed Ring-fused chlorins on cell proliferation of ocular melanoma. Methods. Human cell line MP-41 and a canine primary culture were subjected to the photosensitizers at concentrations between 0,5-1000 nM for 24 hours. The cells were irradiated with 10J (ƛ>570nm). Control groups included: untreated cells and cells submitted only to the administration vehicle (dimethylsulfoxide). The cytotoxicity (MTT) assessment was performed 24 hours after photodynamic therapy (PDT). Results. The dihydroxymethyl ring-fused chlorin (PS1) was the most active, with an IC50 value of 95.1 nM. The dihydroxymethyl-Pt(II) ring-fused chlorin (PS3) also showed promising photodynamic activity with an IC50 value of 114.8nM in MP-41 cells. These chlorins also showed highly satisfactory results in canine cells, with IC50 of 0.6nM for the PS1 and 2.2 nM for PS3. The dicarboxylic acid ring-fused chlorin (PS2) and dicarboxylic acid Pt(II) ring-fused chlorin (PS4) were less efficient in both ocular melanoma cells. PDT had a direct effect on ocular melanoma cell metabolic activity. High activity was obtained at very low concentrations. Conclusion. Satisfactory outcomes were achieved using new photosensitizers, particularly PS1 and PS3. The photosensitizers used are promising, particularly PS1 and PS3. This approach might become an option in treating eye melanoma in medicine and veterinary medicine. Supported by FCT, Portugal, SFRH/BD/139319/2018, SFRH/BD/116794/2016, UID/NEU/04539/2019, UIDB/04539/2020, UIDP/04539/2020 and POCI-01-0145-FEDER-007440. None.por
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dc.identifier.authoremailnmla@uevora.pt
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dc.identifier.citationGuimarães, T. G., Carvalho, G.T.A.P., Mamede, F.V. , Cardoso, K.M., Marto, C.M., Teixo, R.,, & Pereira, N. A. M., Piñeiro, M., Pinho e Melo,T.M.V.D. , Alexandre, N.M.L. ,Botelho, M.F., Laranjo, M. (2022). IN VITRO PHOTODYNAMIC THERAPY ON OCULAR MELANOMA CELLS. 53nd Annual Meeting of the American College of Veterinary Ophtalmologists(ACVO) Palm Springs, CA, USA.por
dc.identifier.comunicacaoPoster
dc.identifier.localPalm Springs, California,USA
dc.identifier.pagina1
dc.identifier.scientificarea206por
dc.identifier.urihttp://hdl.handle.net/10174/34579
dc.identifier.withinvitedoralpresentationnaopor
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dc.language.isoporpor
dc.rightsopenAccesspor
dc.subjectOcularpor
dc.subjectMelanomapor
dc.subjectPhotodynamicpor
dc.subjectTherapypor
dc.subjectPhotosensitizerspor
dc.subjectCellpor
dc.titleIN VITRO PHOTODYNAMIC THERAPY ON OCULAR MELANOMA CELLSpor
dc.typelecturepor

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