Pregled bibliografske jedinice broj: 1282203
Amphiphilic cationic tripyridiniumporphyrins and their Zn(II) complexes: the influence of the irradiation wavelength and the length of the alkyl chain
Amphiphilic cationic tripyridiniumporphyrins and their Zn(II) complexes: the influence of the irradiation wavelength and the length of the alkyl chain // 23rd Annual Conference of the Italian Society of Photobiology
Lecce, Italija, 2023. str. 41-41 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1282203 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Amphiphilic cationic tripyridiniumporphyrins and
their Zn(II) complexes: the influence of the
irradiation wavelength and the length of the alkyl
chain
Autori
Mušković, Martina ; Lončarić, Martin ; Ratkaj, Ivana ; Malatesti, Nela
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
23rd Annual Conference of the Italian Society of Photobiology
Mjesto i datum
Lecce, Italija, 28.06.2023. - 30.06.2023
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Photodynamic therapy ; Amphiphilic porphyrins ; Singlet oxygen ; Melanoma cells
Sažetak
Amphiphilic porphyrins are increasingly proving to be effective photosensitizers (PSs) and promising for the use in photodynamic therapy (PDT) [1]. In our previous research, cationic porphyrins conjugated with a long alkyl chain (18C) showed much higher cytotoxicity on different cell lines compared to a hydrophilic analogue with an acetamido group [2]. Chelation with zinc(II) ion is expected to increase the lifetime of the triplet excited state (3PS*) and improve singlet oxygen production [3]. Since chelation reduces the number of Q bands from four to two with negligible absorption above 610 nm, activation of Zn(II) porphyrins with red light common to PDT is unlikely to be effective, while orange light is much better suited to their optical properties, which still penetrates tissue relatively well. We will present the preparation of free-bases and Zn(II) complexes of N-methylated tripyridinium-3-ylporphyrins conjugated with alkyl chains of different lengths (1C, 8C-18C) and a study of the influence of their lipophilicity on PDT activity against melanoma cell lines. This study includes the determination of photophysical and photochemical properties in different solvents using various spectroscopic methods (UV-VIS and fluorescence spectroscopy, laser flash photolysis (LFP) and time-resolved fluorescence spectroscopy (TRF)) as well as in vitro biological analyses on two different melanoma cell lines (A375 and MeWo) and human dermal fibroblasts (HDF), where cellular uptake of each PS, its intracellular localisation and cytotoxicity were investigated. In addition, the MTT assay was used to compare the application of two different wavelengths for photoactivation of the PSs, red (645 nm ; 2.0 mW / cm2 ) and orange light (607 nm ; 2.0 mW / cm2).
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija, Interdisciplinarne prirodne znanosti, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
POVEZANOST RADA
Projekti:
NadSve-Sveučilište u Rijeci-uniri-prirod-18-173 - Priprema lipidnih konjugata piridilporfirina, njihova karakterizacija i fotodinamička aktivnost (Malatesti, Nela, NadSve - UNIRI projekti 2018) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Sveučilište u Rijeci - Odjel za biotehnologiju
Profili:
Nela Malatesti
(autor)
Ivana Ratkaj
(autor)
Martina Mušković
(autor)
Martin Lončarić
(autor)