N. Vanderveen et al., PHOTOBLEACHING DURING AND RE-APPEARANCE AFTER PHOTODYNAMIC THERAPY OFTOPICAL ALA-INDUCED FLUORESCENCE IN UVB-TREATED MOUSE SKIN, International journal of cancer, 72(1), 1997, pp. 110-118
Photodynamic therapy (PDT) using protoporphyrin IX (PpIX) induced by t
opically applied 5 aminolevulinic acid (ALA) seems a promising alterna
tive for the treatment of superficial non-melanoma skin cancer and act
inic keratosis. In this study, the kinetics of new PpIX fluorescence a
rising after a PDT treatment that had photobleached the original fluor
escence were determined, Our purpose was to examine the feasibility of
multiple irradiations, following a single topical ALA application, to
increase PDT efficacy, In addition, photobleaching during PDT and the
fluorescence spectra during and after PDT were studied, As a model we
used hairless mice with and without UVB-induced skin lesions, ALA was
applied to the skin for 4 kr, An illumination war; delivered either i
mmediately after application or 6 hr after the end of the application
(at interval of maximum fluorescence), During PDT, the fluorescence of
normal skin decreased at a faster rate than the fluorescence of the s
kin lesions, In the fluorescence study after PDT, the areas treated im
mediately post-application showed a fluorescence increase over time si
milar to that in non-treated areas on the same mice. A remarkable resu
lt was that the fluorescence of areas treated at maximum fluorescence
increased, whereas the fluorescence of non-treated areas did not incre
ase over time, With both treatment intervals the new fluorescence show
ed a characteristic PpIX spectrum, Our results demonstrate that a seco
nd illumination, when new PpIX fluorescence has been formed, may incre
ase PDT efficacy after topical ALA application, This finding has been
demonstrated previously Tar systemic ALA administration. (C) 1997 Wile
y-Liss, Inc.