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Subcellular photodynamic action sites of sulfonated aluminum phthalocyanines in a human melanoma cell line

机译:人黑素瘤细胞系中磺化铝酞菁的亚细胞光动力学作用位点

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Abstract: By means of scanning and transmission electron microscopy the subcellular target sites of photodynamic therapy (PDT) with derivatives of sulfonated aluminum phthalocyanine (AlPcS$-1$/, AlPcS$-2$/, AlPcS$-3$/, and AlPcS$-4$/) were studied in a human melanoma LOX cell line. It was found that PDT with AlPcS$-1$/ or AlPcS$-2$/ damaged mainly the biomembraneous system of the cells, such as cytoplasmic membrane, mitochondria, endoplasmic reticulum, etc., while AlPcS$-3$/- or AlPcS$-4$/- induced PDT largely destroyed the lysosomes. However, none of the AlPcS$-n$/s led to nuclear damage at an early stage after PDT. The subcellular photodynamic targets of the derivatives of AlPcS$-n$/ are related to the subcellular localization pattern of the dye in the LOX cells. !21
机译:摘要:通过扫描和透射电镜,用磺化铝酞菁衍生物(AlPcS $ -1 $ /,AlPcS $ -2 $ /,AlPcS $ -3 $ /和AlPcS的衍生物)进行光动力疗法(PDT)的亚细胞靶位在人黑素瘤LOX细胞系中研究了$ -4 $ /。发现具有AlPcS $ -1 $ /或AlPcS $ -2 $ /的PDT主要破坏细胞的生物膜系统,例如细胞质膜,线粒体,内质网等,而AlPcS $ -3 $ /-或AlPcS $ -4 $ /-诱导的PDT在很大程度上破坏了溶酶体。但是,在PDT之后的早期阶段,没有一个AlPcS $ -n $ / s导致核损害。 AlPcS $ -n $ /的衍生物的亚细胞光动力学靶标与该染料在LOX细胞中的亚细胞定位模式有关。 !21

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