Photosensitizing Potencies of the Structural Analogues of Benzoporphyrin Derivative in Different Biological Test Systems
- 1 October 1996
- journal article
- research article
- Published by Mary Ann Liebert Inc in Journal of Clinical Laser Medicine & Surgery
- Vol. 14 (5) , 335-341
- https://doi.org/10.1089/clm.1996.14.335
Abstract
Benzoporphyrin derivative (BPD) is a potent photosensitizer in biological systems. There are four structural analogues of BPD. The analogues share the same chromophor, which results in their having almost identical optical spectra, extinction coefficients, and yields of singlet oxygen. Small structural differences affect their photosensitizing potency in various biological systems, and thus make them an interesting tool to study the structure–activity relationship. The ranking of the photosensitizing potency of the analogues differed depending on the test system. The more efficient photosensitization of tumor cell lines by the highly lipophilic monoacids as compared to that by less lipophilic diacids correlated positively with the partition coefficient, and was related to the rate of diffusion into the cells. However, in the assay systems where PDT targets were located in the membrane (red blood cells hemolysis, enveloped vesicular stomatitis virus, isolated mitochondria) there was very little difference in photosensitizing potency of BPD analogues. The results indicate that the evaluation of photosensitizers is affected by the test system and thus for photosensitizers screening purposes, the choice of the test system should be made based on the intended ultimate use.Keywords
This publication has 25 references indexed in Scilit:
- Structure‐Photodynamic Activity Relationships of a Series of 4‐Substituted Zinc PhthalocyaninesPhotochemistry and Photobiology, 1996
- The Use of Transcutaneous Photodynamic Therapy in the Prevention of Adjuvant-Enhanced Arthritis in MRL/lpr MiceClinical Immunology and Immunopathology, 1994
- PHOTOPHYSICAL AND PHOTOSENSITIZING PROPERTIES OF BENZOPORPHYRIN DERIVATIVE MONOACID RING A (BPD‐MA)*Photochemistry and Photobiology, 1994
- APOPTOSIS DURING PHOTODYNAMIC THERAPY‐INDUCED ABLATION OF RIF‐1 TUMORS IN C3H MICE: ELECTRON MICROSCOPIC, HISTOPATHOLOGIC AND BIOCHEMICAL EVIDENCEPhotochemistry and Photobiology, 1993
- In vitro AND in vivo UPTAKE OF BENZOPORPHYRIN DERIVATIVE INTO HUMAN AND MINISWINE ATHEROSCLEROTIC PLAQUEPhotochemistry and Photobiology, 1993
- Biodistribution of tritiated benzoporphyrin derivative (3H-BPD-MA), a new potent photosensitizer, in normal and tumor-bearing miceJournal of Photochemistry and Photobiology B: Biology, 1990
- A NEW HYPOTHESIS FOR THE TARGET IN PHOTOHEMOLYSIS: DIMERS OF THE BAND 3 PROTEINPhotochemistry and Photobiology, 1986
- Effects of photodynamic action on energy coupling of Ca 2+ uptake in liver mitochondriaBiochemical and Biophysical Research Communications, 1983
- PHOTODYNAMIC EFFECTS INDUCED BY FUROCOUMARINS ON A MEMBRANE SYSTEM. COMPARISON WITH HEMATOPORPHYRINPhotochemistry and Photobiology, 1982