Abstract | BACKGROUND: MATERIALS AND METHODS: In order to complete our studies we decided to use photosensitizers, i.e. dithiaporphyrin (DTP) and sulfoxaporphyrin (OXA) in combination with halogen lamp irradiation of presensitized tumors. The doses of sensitizers were: 2.5, 5.0, 7.5 and 10.0 mg/kg of body weight and total light doses were: 50, 100 and 150 J/sq.cm at the selected wavelength. Following such a treatment we have evaluated tumor necrosis of BFS1 fibrosarcoma growing on BALB/c mice. Together with tumor necrosis evaluation we have examined skin response to photodynamic treatment. RESULTS: We have found that both new sensitizers caused significant tumor damage at no skin alterations. The induction of tumor necrosis seemed to be dose dependent, i.e. higher photodynamic doses (sensitizer dose x light dose) resulted in more severe damage to the tumors than the lower doses. CONCLUSION: Our study showed that BFS1 fibrosarcoma is highly sensitive to PDT after application of new sensitizers. Both compounds can be considered as potent tumor photosensitizers in future clinical trials.
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Authors | K Symonowicz, P Ziólkowski, P Chmielewski, L Latos-Grazynski, J Rabczynski, B J Osiecka, J Milach |
Journal | Anticancer research
(Anticancer Res)
1999 Nov-Dec
Vol. 19
Issue 6B
Pg. 5385-91
ISSN: 0250-7005 [Print] Greece |
PMID | 10697566
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- 21,23-dithiaporphyrin
- 21-oxaporphyrin
- Photosensitizing Agents
- Porphyrins
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Topics |
- Animals
- Fibrosarcoma
(drug therapy, pathology)
- Mice
- Mice, Inbred BALB C
- Photochemotherapy
- Photosensitizing Agents
(pharmacology, therapeutic use)
- Porphyrins
(pharmacology, therapeutic use)
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