Transdermal delivery system to release phthalocyanine photosensitizers for the potential treatment of skin cancer with PDT

dc.authorid0000-0002-8720-8087
dc.authorid0000-0003-0212-0973
dc.authorid0000-0001-7915-5168
dc.authorid0000-0003-2108-0452
dc.authorid0000-0001-9376-1770
dc.contributor.authorÇamur Demir, Meryem
dc.contributor.authorKurşun Baysak, Fatma
dc.contributor.authorBoyar, Caner Yahya
dc.contributor.authorToksoy, Alihan
dc.contributor.authorAlgı, Fatih
dc.date.accessioned2024-07-18T12:47:37Z
dc.date.available2024-07-18T12:47:37Z
dc.date.issued2024
dc.departmentSabire Yazıcı Fen Edebiyat Fakültesi
dc.description.abstractThis research aims to examine the transdermal release of water-soluble indium and zinc metallo phthalocyanine (InPc and ZnPc) compounds from the poly(vinyl alcohol) (PVA) membrane and the cytotoxicity effect of these Pcs on normal mouse fibroblasts (L929 fibroblast) and human melanoma (SK-MEL-30) cells. For this purpose, the effects of temperature, pH, drug concentration and membrane thickness on transdermal release were investigated in order to obtain the optimum transdermal release profile by preparing PVA membranes with different thicknesses and crosslinked by heat treatment. Optimum drug release was found to be 85.36% using 6 µm thick PVA membrane at 37 ± 0.5 °C, when upper cell pH 1.2 and lower cell pH 5.5, for 3 mg/mL InPc drug concentration. Under the same conditions, the drug release value for ZnPc was found to be 69.78%. In addition, in vitro studies were performed on L929 and SK-MEL-30 cells. under optimized drug (InPc and ZnPc) and membrane conditions. It was found that no significant cytotoxic effect was observed in L929 and SK-MEL-30 cells in the dark. Photodynamic tests were also carried out with InPc and ZnPc. The results show that cell viability decreases in SK-MEL-30 cells at concentrations of 10 µg/mL and above. In addition, while the InPc IC50 value was determined as 4.058 µg/mL, this value was determined as 11.574 µg/mL for ZnPc.
dc.identifier.doi10.55730/1300-0527.3666
dc.identifier.endpage386en_US
dc.identifier.issn1300-0527
dc.identifier.issue2en_US
dc.identifier.scopusqualityQ3
dc.identifier.startpage376en_US
dc.identifier.urihttps:/dx.doi.org/10.55730/1300-0527.3666
dc.identifier.urihttps://hdl.handle.net/20.500.12451/12164
dc.identifier.volume48en_US
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTUBITAK
dc.relation.ispartofTurkish Journal of Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rightsinfo:eu-repo/semantics/embargoedAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subjectPhthalocyanines
dc.subjectPoly(vinyl alcohol)
dc.subjectSK-MEL-30
dc.subjectTransdermal Drug Delivery
dc.titleTransdermal delivery system to release phthalocyanine photosensitizers for the potential treatment of skin cancer with PDT
dc.typeArticle

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