Paper
17 March 1989 Chemical Principles In The Design Of Improved Porphyrin Photosensitizers
B. Franck, G. Fulling, M . Gosmann, G. Kniibel, H. Mertes, D. Schroder
Author Affiliations +
Proceedings Volume 0997, Advances in Photochemotherapy; (1989) https://doi.org/10.1117/12.960192
Event: O-E/Fiber LASE '88, 1988, Boston, MA, United States
Abstract
Due to the encouraging results with hematoporphyrin in photochemotherapy the porphyrin system gained predominant importance for this important medicinal application. By some convenient chemical reactions hematoporphyrin can be converted to improved derivatives, which are homogeneous, stable, and excellently soluble. Novel enlarged "porphyrinoids" with two, four, and eight additional double bonds inserted into the porphyrin ring system were synthesized. With intensive VIS absorption bands, shifted up to 300 nm to longer wave lengths compared with the normal porphyrins, these porphyrinoids may be promising for more selective and penetrating phototherapy. All the new porphyrin derivatives were shown to be efficient photosensitizers with respect to the production of singlet oxygen.
© (1989) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
B. Franck, G. Fulling, M . Gosmann, G. Kniibel, H. Mertes, and D. Schroder "Chemical Principles In The Design Of Improved Porphyrin Photosensitizers", Proc. SPIE 0997, Advances in Photochemotherapy, (17 March 1989); https://doi.org/10.1117/12.960192
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KEYWORDS
Oxygen

Absorption

Tumors

Tissue optics

Phototherapy

Toxicity

Skin

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