5,10,15,20-Tetrakis(4-sulfonatophenyl)porphyrin Zinc and Chloro-aluminum Phthalocyanine Disulfonate in Photodynamic Therapy of Colorectal Adenocarcinoma In Vitro
Jazyk angličtina Země Řecko Médium print
Typ dokumentu časopisecké články
PubMed
39348959
DOI
10.21873/anticanres.17263
PII: 44/10/4339
Knihovny.cz E-zdroje
- Klíčová slova
- Colorectal adenocarcinoma, DNA fragmentation, photodynamic therapy, phthalocyanines, porphyrins, reactive oxygen species,
- MeSH
- adenokarcinom * farmakoterapie metabolismus patologie MeSH
- buňky HT-29 MeSH
- fotochemoterapie * metody MeSH
- fotosenzibilizující látky * farmakologie MeSH
- indoly * farmakologie MeSH
- kolorektální nádory * farmakoterapie patologie metabolismus MeSH
- lidé MeSH
- metaloporfyriny * farmakologie MeSH
- organokovové sloučeniny * farmakologie MeSH
- poškození DNA účinky léků MeSH
- reaktivní formy kyslíku * metabolismus MeSH
- viabilita buněk účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- fotosenzibilizující látky * MeSH
- indoly * MeSH
- metaloporfyriny * MeSH
- organokovové sloučeniny * MeSH
- reaktivní formy kyslíku * MeSH
- zinc-tetrakis(p-sulfonatophenyl)porphyrin MeSH Prohlížeč
BACKGROUND/AIM: Colorectal cancer (CRC) is one of the most widespread malignancies. One of the alternative therapeutic methods appears to be photodynamic therapy (PDT). MATERIALS AND METHODS: This study investigated the efficiency of 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin zinc (ZnTPPS4) and chloro-aluminum phthalocyanine disulfonate (ClAlPcS2) with two commercial photosensitive compounds 5,10,15,20-tetrakis(1-methylpyridinium-4-yl)porphyrin (TMPyP) and tetramethylthionine chloride (methylene blue, MB) in PDT for CRC in vitro. In addition to the study of the photodynamic effect on the viability of the colorectal carcinoma cell line HT29, cellular uptake, ROS production, and DNA damage were investigated. RESULTS: All photosensitizers showed good accumulation within HT29 cells, high efficiency in killing the cells, and a concentration-dependent increase in the production of ROS. CONCLUSION: PDT using ZnTPPS4 and ClAlPcS2 may be effective in the treatment of CRC, achieving a similar photocytotoxic effect at much lower concentrations compared to MB.
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