4.6 Article

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

Journal

PHARMACEUTICALS
Volume 14, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/ph14050433

Keywords

PDT; methyl aminolevulinate; methylene blue; riboflavin; photosensitizing agents; ultraviolet radiation; skin tumors; prophylactic treatment; hairless mice

Funding

  1. Hofbundtmager Aage Bangs Foundation

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In this study, methylene blue (MB) and riboflavin (RF) did not show significant effectiveness in preventing skin tumors induced by ultraviolet radiation, while methyl aminolevulinate (MAL) was proven to be an effective prophylactic treatment against UVR-induced skin tumors in hairless mice.
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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