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Authordc.contributor.authorLissi Gervaso, Eduardo A. 
Authordc.contributor.authorSalim-Hanna, Marta 
Authordc.contributor.authorFauré, M. 
Authordc.contributor.authorVidela Cabrera, Luis 
Admission datedc.date.accessioned2019-01-29T15:47:30Z
Available datedc.date.available2019-01-29T15:47:30Z
Publication datedc.date.issued1991
Cita de ítemdc.identifier.citationXenobiotica, Volumen 21, Issue 8, 2018, Pages 995-1001
Identifierdc.identifier.issn00498254
Identifierdc.identifier.other10.3109/00498259109039539
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/162378
Abstractdc.description.abstract1. 2,2'Azo-bis-amidinopropane (ABAP) thermal decomposition produces free radicals that initiate the lipid peroxidation of erythrocyte ghost membranes. 2. Addition of 6-n-propyl-2-thiouracil decreases the rate of the process, both by decreasing consumption of the natural antioxidants of the membranes and by direct interaction with the free radicals involved in the lipid peroxidation. 3. Peroxyl radicals produced in ABAP thermal decomposition inactivate lysozyme, horseradish peroxidase (HRP) and glucose oxidase, in that order. The number of enzyme molecules inactivated per radical introduced into the system increases with enzyme concentration. 4. Competitive studies employing mixtures of enzymes show that the order of reactivity of these enzymes towards the peroxyl radicals is the opposite to that obtained for the rate of enzyme inactivation. It is concluded that inactivation efficiency is determined mainly by the average number of free radicals that must react with an enzyme molecule to
Lenguagedc.language.isoen
Publisherdc.publisherInforma Healthcare
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceXenobiotica
Keywordsdc.subjectBiochemistry
Keywordsdc.subjectToxicology
Keywordsdc.subjectPharmacology
Keywordsdc.subjectHealth, Toxicology and Mutagenesis
Títulodc.title2,2'azo-bis-amidinopropane as a radical source for lipid peroxidation and enzyme inactivation studies
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile