A Skin Cancer Prophylaxis Study in Hairless Mice Using Methylene Blue, Riboflavin, and Methyl Aminolevulinate as Photosensitizing Agents in Photodynamic Therapy

被引:8
作者
Wulf, Hans Christian [1 ]
Al-Chaer, Rami Nabil [1 ]
Glud, Martin [1 ]
Philipsen, Peter Alshede [1 ]
Lerche, Catharina Margrethe [1 ,2 ]
机构
[1] Copenhagen Univ Hosp, Dept Dermatol, DK-2400 Copenhagen, Denmark
[2] Univ Copenhagen, Dept Pharm, DK-2100 Copenhagen, Denmark
关键词
PDT; methyl aminolevulinate; methylene blue; riboflavin; photosensitizing agents; ultraviolet radiation; skin tumors; prophylactic treatment; hairless mice; BASAL-CELL CARCINOMA; ACTINIC KERATOSES; DELIVERY; PHOTOCARCINOGENESIS; PHOTOACTIVATION; MULTICENTER; EXPOSURE; SURGERY;
D O I
10.3390/ph14050433
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The high incidence of sunlight-induced human skin cancers reveals a need for more effective photosensitizing agents. In this study, we compared the efficacy of prophylactic photodynamic therapy (PDT) when methylene blue (MB), riboflavin (RF), or methyl aminolevulinate (MAL) were used as photosensitizers. All mice in four groups of female C3.Cg/TifBomTac hairless immunocompetent mice (N = 100) were irradiated with three standard erythema doses of solar-simulated ultraviolet radiation (UVR) thrice weekly. Three groups received 2 x 2 prophylactic PDT treatments (days 45 + 52 and 90 + 97). The PDT treatments consisted of topical administration of 16% MAL, 20% MB, or 20% RF, and subsequent illumination that matched the photosensitizers' absorption spectra. Control mice received no PDT. We recorded when the first, second, and third skin tumors developed. The pattern of tumor development after MB-PDT or RF-PDT was similar to that observed in irradiated control mice (p > 0.05). However, the median times until the first, second, and third skin tumors developed in mice given MAL-PDT were significantly delayed, compared with control mice (256, 265, and 272 vs. 215, 222, and 230 days, respectively; p < 0.001). Only MAL-PDT was an effective prophylactic treatment against UVR-induced skin tumors in hairless mice.
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页数:11
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