Scavenging of photogenerated singlet molecular oxygen and superoxide radical anion by sulpha drugs - Kinetics and mechanism
Authors:
- Marta DíazMDMarta Díaz
- Marta LuizMLMarta Luiz
- Sonia BertolottiSBSonia Bertolotti
- Sandra MiskoskiSMSandra Miskoski
- Norman A GarcíaNGNorman A García
- 1 December 2004
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 82 (12) , 1752-1759
Abstract
The ability of the sulfanilic antibiotics (SDs), dapsone (DAP), sulfisoxazole (SFX), sulfadiazine (SFD), and sulfanilic acid (SFNA) to act as scavengers of the visible-light-photogenerated species superoxide radical anion (O2·) and singlet molecular oxygen (O2(1Δg)) was studied employing the natural pigment riboflavin (Rf) and the artificial dye Rose Bengal as photosensitisers. A complex mechanism, common to all the SDs studied, was elucidated through stationary photolysis, polarographic detection of oxygen uptake, fluorescence spectroscopy, time-resolved phosphorescence detection of O2(1Δg), and laser flash photolysis. Visible-light irradiation of aqueous and aqueous methanolic solutions of Rf (ca. 0.02 mmol/L) plus SD (ca. 0.5 mmol/L) photogenerated excited singlet and triplet Rf (1Rf* and 3Rf*). Under these experimental conditions, only 3Rf* is quenched either by oxygen, giving rise to O2(1Δg) by electronic energy transfer to dissolved ground-state oxygen, or by SD, yielding semireduced Rf through an electron-transfer process. Complementary experiments performed in pure water employing superoxide dismutase and sodium azide inhibition of oxygen uptake, in parallel with laser flash photolysis data, showed that O2· is also formed, probably due to the reaction of the anion radical from Rf with dissolved oxygen, yielding also neutral, ground-state Rf. Both active oxygen species, namely, O2· and O2(1Δg), are quenched by the SDs and, as a result, photodegradation of the SDs — each to a different extent — and photodegradation of the sensitiser itself were observed. The SDs that kinetically behave as the better physical quenchers of O2(1Δg), which are in principle good candidates as photoprotectors, namely, DAP and SFD, suffer photooxidation, exhibiting high to moderate oxygen consumption rates due to the O2· oxidative pathway, whereas for SFNA and SFX, oxidation predominantly occurs through an O2(1Δg)-mediated mechanism. Microbiological results for SFX, taken as a representative SD, indicate that the photodegradation of the drug, upon visible-light Rf-sensitised irradiation, is accompanied by a net loss in bacteriostatic activity.Key words: photooxidation, singlet oxygen, superoxide radical anion, sulpha drugs.Keywords
This publication has 21 references indexed in Scilit:
- Kinetic study of the riboflavin-sensitised photooxygenation of two hydroxyquinolines of biological interestJournal of Photochemistry and Photobiology B: Biology, 2003
- Environmental photodegradation of pyrimidine fungicides — Kinetics of the visible-light-promoted interactions between riboflavin and 2-amino-4-hydroxy-6-methylpyrimidineCanadian Journal of Chemistry, 2002
- Riboflavin (VB2) photosensitized oxidation of 2′-deoxyguanosine-5′-monophosphate (dGMP) in aqueous solution: a transient intermediates studyPhysical Chemistry Chemical Physics, 2000
- The Photoinitiation Mechanism of Vinyl Polymerization by Riboflavin/Triethanolamine in Aqueous MediumMacromolecules, 1999
- Stepwise Two‐Photon Excitation of 1,5‐Dihydroflavin Mononucleotide: Study of Flavosemiquinone PropertiesPhotochemistry and Photobiology, 1997
- A STUDY OF THE PHOTODYNAMIC EFFICIENCIES OF SOME EYE LENS CONSTITUENTSPhotochemistry and Photobiology, 1991
- Dark and photoinduced interactions between riboflavin and indole auxinsCollection of Czechoslovak Chemical Communications, 1991
- Singlet oxygen photogeneration by ionized and un-ionized derivatives of Rose Bengal and Eosin Y in diluted solutionsJournal of Photochemistry and Photobiology A: Chemistry, 1990
- Singlet oxygen in surface waters. 3. Photochemical formation and steady-state concentrations in various types of watersEnvironmental Science & Technology, 1986
- THE PHOTOCHEMISTRY OF RIBOFLAVIN—V. THE PHOTODEGRADATION OF ISOALLOXAZINES IN ALCOHOLIC SOLVENTSPhotochemistry and Photobiology, 1977