The aim of this study was to explore the antiradical activity of Met I (an active metabolite of erdosteine) containing a pharmacologically active sulphydryl group, by means of electron paramagnetic resonance (EPR) spectroscopy which has not previously been used to characterize the antiradical activity of Met I. The effects of concentrations of 20, 10, 5, 2.5, 1.25 and 0.625 μg/ml of Met I were tested against: (a) the Fenton reaction model system with EPR detection of HO·; (b) the KO2-crown ether system with EPR detection of O2-·; (c) the EPR assay based on the reduction of the Tempol radical, and (d) the EPR assay based on the reduction of Fremy's salt radical. Our findings show that the intensity of 4 different free radicals was significantly reduced in the presence of Met I, thus indicating the presence of a termination reaction between the free radicals and Met I. Copyright

Free radical scavenging activity of Erdosteine metabolite I investigated by Electron Paramagnetic Resonance spectroscopy / P. Braga, M. Culici, M. Dal Sasso, M. Falchi. - In: PHARMACOLOGY. - ISSN 0031-7012. - 85:4(2010 Mar 06), pp. 195-202. [10.1159/000275063]

Free radical scavenging activity of Erdosteine metabolite I investigated by Electron Paramagnetic Resonance spectroscopy

P. Braga
Primo
;
M. Falchi
Ultimo
2010

Abstract

The aim of this study was to explore the antiradical activity of Met I (an active metabolite of erdosteine) containing a pharmacologically active sulphydryl group, by means of electron paramagnetic resonance (EPR) spectroscopy which has not previously been used to characterize the antiradical activity of Met I. The effects of concentrations of 20, 10, 5, 2.5, 1.25 and 0.625 μg/ml of Met I were tested against: (a) the Fenton reaction model system with EPR detection of HO·; (b) the KO2-crown ether system with EPR detection of O2-·; (c) the EPR assay based on the reduction of the Tempol radical, and (d) the EPR assay based on the reduction of Fremy's salt radical. Our findings show that the intensity of 4 different free radicals was significantly reduced in the presence of Met I, thus indicating the presence of a termination reaction between the free radicals and Met I. Copyright
Settore BIO/14 - Farmacologia
6-mar-2010
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/144375
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