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PHOTODYNAMIC ACTIVITIES and SKIN PHOTOSENSITIVITY OF THE bis(DIMETHYLTHEXYLSILOXY)SILICON 2,3‐NAPHTHALOCYANINE IN MICE
Author(s) -
Brasseur Nicole,
Ouellet Rene,
Lewis Karina,
Potter William R.,
Lier Johan E. van
Publication year - 1995
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/j.1751-1097.1995.tb02409.x
Subject(s) - photodynamic therapy , chemistry , in vivo , sinc function , photosensitivity , absorption (acoustics) , pharmacokinetics , hematoporphyrin , biophysics , pharmacology , materials science , medicine , biology , organic chemistry , microbiology and biotechnology , optoelectronics , computer science , composite material , computer vision
The photodynamic therapy (PDT) activity of the bis (dimethylthexylsiloxy)silicon 2,3‐na‐phthalocyanine (SiNc 8 ) was evaluated against the EMT‐6 tumor implanted intradermally in BALB/c mice. The SiNc 8 was formulated in aqueous emulsions based on Cremophor EL or Solutol HS 15. The formulation was shown to affect plasma clearance and overall pharmacokinetics. Compared to Cremophor, Solutol promoted rapid plasma clearance and high liver retention of the dye, combined with a slight increase of dye tumor concentrations. The PDT action spectrum for tumor response of SiNc 8 in Cremophor (190 mW cm 2 , 200 J cm 2 , 24 h postinjection [p.i.] of 1 (jimol kg 1 ) showed a maximum at 780 nm, which corresponds to the absorption maximum of the monomelic dye as well as the in vivo maximum change in the “diffuse optical density” produced by the dye. The extent of tumor necrosis increased with augmented dye and light doses. Regardless of the formulation, at 1 h p.i. of 0.1 μmol kg −! SiNc 8 , PDT efficiency (190 mW cm' 2 , 400 J cm 2 ) was high but accompanied by severe damage to normal tissues, at 24 h PDT resulted in complete tumor regression in 80% of the animals without adverse effects to adjacent tissues, while at 72 h p.i. PDT induced no tumor response with Cremophor and only a partial response with Solutol. At the latter time point, plasma dye clearance was nearly complete while tumor tissue levels remained high, suggesting that tumor response correlates with plasma rather than tumor dye levels. Skin sensitivity of SKhl mice to solar‐simulated radiation was lower with SiNc 8 as compared to Photofrin®. Our data suggest the potential of SiNc 8 as a far‐red absorbing photosensitizer in clinical PDT.