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Topical application of a novel porphycene dye for photodynamic therapy:penetration studies in human perilesional skin and basal cell carcinoma,

机译:一种新型卟啉染料在光动力疗法中的局部应用:在人类皮损周围皮肤和基底细胞癌中的渗透研究,

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Abstract: PDT in dermatology is of growing interest and there are efforts to develop new sensitizers for topical application. Penetration potency of 9-acetoxy-2,7,12,17-tetrakis-($beta@- methoxyethyl)-porphycene (ATMPn), a novel sensitizer for topical photodynamic therapy, was studied in perilesional normal human skin from 58 melanoma patients and basal cell carcinomas of 12 patients. Single specimens of freshly excised perilesional skin (n equals 368) and basal cell carcinomas (n equals 28) were evaluated after topical application of an ATMPn solution for different time intervals (2, 6, 16 h) and subsequent preparation of cryostate sections (10 micrometer). Fluorescence distribution in tissue sections was estimated qualitatively using a score system respecting the morphological structure of human skin. In all examined sections of perilesional skin red fluorescence indicative of ATMPn was seen down to the basal layer of the epidermis using epifluorescence microscopy and optical multichannel analysis. Longer incubation times (16 - 20 h) revealed significant higher score sums as compared to incubation times of 2 or 6 h. However, basal cell carcinomas did not show time dependent differences in penetration. After 6 h penetration of ATMPn into the tumor, cell nests in the deep dermis were detected. These results indicate that there might be a faster penetration of this sensitizer in tumorous tissue as in normal tissue after topical application. !9
机译:摘要:皮肤病学中的PDT引起了越来越多的兴趣,并且正在努力开发用于局部应用的新型敏化剂。研究了58种黑色素瘤患者的病灶周围正常人皮肤中9-乙酰氧基-2,7,12,17-四(-(β@-甲氧基乙基)-卟啉(ATMPn)的渗透效力,这是一种用于局部光动力疗法的新型敏化剂。基底细胞癌12例。在局部时间间隔(2、6、16 h)局部应用ATMPn溶液并随后准备冷冻切片时(10),对新鲜切除的病灶周围皮肤(n等于368)和基底细胞癌(n等于28)的单个标本进行了评估。千分尺)。使用计分系统,根据人体皮肤的形态结构,定性评估组织切片中的荧光分布。使用落射荧光显微镜和光学多通道分析,在所有病灶周围皮肤的切片中,直到表皮基底层都看到了指示ATMPn的红色荧光。与2到6小时的孵育时间相比,更长的孵育时间(16-20小时)显示出明显更高的分数总和。但是,基底细胞癌的渗透率没有时间依赖性。在ATMPn渗透到肿瘤中6小时后,在深层真皮中检测到细胞巢。这些结果表明,与局部施用后的正常组织中一样,该敏化剂在肿瘤组织中的渗透可能更快。 !9

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