Verteporfin, photofrin II, and merocyanine 540 as PDT photosensitizers against melanoma cells

التفاصيل البيبلوغرافية
العنوان: Verteporfin, photofrin II, and merocyanine 540 as PDT photosensitizers against melanoma cells
المؤلفون: Anna Pawlak, Martyna Elas, Krystyna Urbanska, Grażyna Stochel, Andrzej Karocki, Patrycja Nowak-Sliwinska
المصدر: Biochemical and Biophysical Research Communications. 349:549-555
بيانات النشر: Elsevier BV, 2006.
سنة النشر: 2006
مصطلحات موضوعية: Porphyrins, genetic structures, Cell Survival, merocyanine 540, Biophysics, chemistry.chemical_element, Quantum yield, Pyrimidinones, Photochemistry, Biochemistry, Oxygen, Mice, Photosensitivity, Cell Line, Tumor, medicine, Animals, Triplet state, Melanoma, Molecular Biology, Cell damage, Photofrin II, singlet molecular oxygen, verteporfin, Photosensitizing Agents, photodynamic effect, photofrin II, Verteporfin, Dose-Response Relationship, Radiation, Cell Biology, medicine.disease, triplet lifetime, eye diseases, Kinetics, Photochemotherapy, chemistry, Dihematoporphyrin Ether, Signal Transduction, medicine.drug
الوصف: The efficiency of photodynamic effect (PDE) for Photofrin II (PfII), Verteporfin, and Merocyanine 540 (MC540) was compared against neoplastic cells. Triplet state lifetimes and singlet molecular oxygen quantum yields were correlated with biological effect. PfII triplet lifetime was two times longer than that of Verteporfin, however, its singlet molecular oxygen quantum yield was two times lower in comparison with Verteporfin. High singlet molecular oxygen quantum yield of Verteporfin resulted in high biological efficacy. To achieve 50% mortality of cells four times lower light dose and five times lower concentration of Verteporfin were applied in comparison with PfII. The same level of cell damage was reached using 10 times higher light dose and two times higher concentration of MC540 in comparison with PfII. Our results confirm that singlet molecular oxygen based mechanism, prevalent for Verteporfin and PfII, was highly effective against melanoma cells. Verteporfin can be used at small doses with high cellular damage efficiency.
تدمد: 0006-291X
DOI: 10.1016/j.bbrc.2006.08.060
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67a00eab472d1e1275398a80bc7152be
https://doi.org/10.1016/j.bbrc.2006.08.060
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....67a00eab472d1e1275398a80bc7152be
قاعدة البيانات: OpenAIRE
الوصف
تدمد:0006291X
DOI:10.1016/j.bbrc.2006.08.060