Photochemical and photobiological properties of furocoumarins and homologues drugs
Furocoumarins are natural photosensitizing drugs used in PUVA photochemotherapy and in photopheresis. Their therapeutic effectiveness is connected to the lesions they induce to various cell components, membranes, ribosomes, mitochondria, and in particular to DNA, damaged by formation of monofunction...
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| Language: | English |
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Wiley
1999-01-01
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| Series: | International Journal of Photoenergy |
| Online Access: | http://dx.doi.org/10.1155/S1110662X9900001X |
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| author | F. Bordin |
| author_facet | F. Bordin |
| author_sort | F. Bordin |
| collection | DOAJ |
| description | Furocoumarins are natural photosensitizing drugs used in PUVA photochemotherapy and in
photopheresis. Their therapeutic effectiveness is connected to the lesions they induce to various cell components,
membranes, ribosomes, mitochondria, and in particular to DNA, damaged by formation of monofunctional
adducts and of inter-strand cross-links (ISC). ISC represent a severe damage, mainly correlated to the
main side effects observed in photochemotherapy, skin phototoxicity and genotoxicity. Searching for new
monofunctional derivatives, two tetramethylfuroquinolinones, 1,4,6,8-tetramethyl-2H-furo[2,3-h]quinolin-2-
one (FQ) and 4,6,8,9-tetramethyl-2H-furo[2,3-h]-quinolin-2-one (HFQ) were studied. Both compounds are very
active; however while FQ produced many chromosomal aberrations and strong skin erythemas, HFQ practically
did not induce such side effects. FQ and HFQ formed high levels of monoadducts but no ISC in DNA,
but both provoked many DNA-protein cross-links (DPC). FQ induced these lesions by a biphotonic reaction:
at first a furan-side monoadduct is formed, which is then converted into a DPC; thus the FQ molecule seemed
to form the bridge between DNA and proteins. HFQ formed DPC by a single step (DPC at zero length, like
UVC). For these features, HFQ appears to be the first molecule belonging to a new class of active but not
phototoxic drugs for photomedicine. |
| format | Article |
| id | doaj-art-515a788645f1480bb35793c0c040255d |
| institution | Kabale University |
| issn | 1110-662X |
| language | English |
| publishDate | 1999-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | International Journal of Photoenergy |
| spelling | doaj-art-515a788645f1480bb35793c0c040255d2025-02-03T01:24:01ZengWileyInternational Journal of Photoenergy1110-662X1999-01-01111610.1155/S1110662X9900001XPhotochemical and photobiological properties of furocoumarins and homologues drugsF. Bordin0Department of pharmaceutical Sciences of Padova University, Padova, ItalyFurocoumarins are natural photosensitizing drugs used in PUVA photochemotherapy and in photopheresis. Their therapeutic effectiveness is connected to the lesions they induce to various cell components, membranes, ribosomes, mitochondria, and in particular to DNA, damaged by formation of monofunctional adducts and of inter-strand cross-links (ISC). ISC represent a severe damage, mainly correlated to the main side effects observed in photochemotherapy, skin phototoxicity and genotoxicity. Searching for new monofunctional derivatives, two tetramethylfuroquinolinones, 1,4,6,8-tetramethyl-2H-furo[2,3-h]quinolin-2- one (FQ) and 4,6,8,9-tetramethyl-2H-furo[2,3-h]-quinolin-2-one (HFQ) were studied. Both compounds are very active; however while FQ produced many chromosomal aberrations and strong skin erythemas, HFQ practically did not induce such side effects. FQ and HFQ formed high levels of monoadducts but no ISC in DNA, but both provoked many DNA-protein cross-links (DPC). FQ induced these lesions by a biphotonic reaction: at first a furan-side monoadduct is formed, which is then converted into a DPC; thus the FQ molecule seemed to form the bridge between DNA and proteins. HFQ formed DPC by a single step (DPC at zero length, like UVC). For these features, HFQ appears to be the first molecule belonging to a new class of active but not phototoxic drugs for photomedicine.http://dx.doi.org/10.1155/S1110662X9900001X |
| spellingShingle | F. Bordin Photochemical and photobiological properties of furocoumarins and homologues drugs International Journal of Photoenergy |
| title | Photochemical and photobiological properties of furocoumarins and homologues drugs |
| title_full | Photochemical and photobiological properties of furocoumarins and homologues drugs |
| title_fullStr | Photochemical and photobiological properties of furocoumarins and homologues drugs |
| title_full_unstemmed | Photochemical and photobiological properties of furocoumarins and homologues drugs |
| title_short | Photochemical and photobiological properties of furocoumarins and homologues drugs |
| title_sort | photochemical and photobiological properties of furocoumarins and homologues drugs |
| url | http://dx.doi.org/10.1155/S1110662X9900001X |
| work_keys_str_mv | AT fbordin photochemicalandphotobiologicalpropertiesoffurocoumarinsandhomologuesdrugs |