<?xml version="1.0"?><rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xmlns:wgs84_pos="http://www.w3.org/2003/01/geo/wgs84_pos" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:rdaGr2="http://rdvocab.info/ElementsGr2" xmlns:oai="http://www.openarchives.org/OAI/2.0/" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:skos="http://www.w3.org/2004/02/skos/core#" xmlns:dcterms="http://purl.org/dc/terms/"><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:doc-JMRGYATZ/4eea1be2-b846-47ab-90ec-f88ca878e93c/HTML"><dcterms:extent>13 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:doc-JMRGYATZ/5f735e61-4b24-419c-94ec-b5e1bf34ca25/PDF"><dcterms:extent>75 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:doc-JMRGYATZ/f13ebfb9-face-4e95-ad8d-24a4dc799647/TEXT"><dcterms:extent>12 KB</dcterms:extent></edm:WebResource><edm:TimeSpan rdf:about="1998-2025"><edm:begin xml:lang="en">1998</edm:begin><edm:end xml:lang="en">2025</edm:end></edm:TimeSpan><edm:ProvidedCHO rdf:about="URN:NBN:SI:doc-JMRGYATZ"><dcterms:isPartOf rdf:resource="https://www.dlib.si/details/URN:NBN:SI:spr-KC6O72BG" /><dcterms:issued>2000</dcterms:issued><dc:creator>Nemec, Marjanca</dc:creator><dc:creator>Pečar, Slavko</dc:creator><dc:creator>Schara, Milan Valter</dc:creator><dc:format xml:lang="sl">številka:1</dc:format><dc:format xml:lang="sl">letnik:47</dc:format><dc:format xml:lang="sl">8 strani</dc:format><dc:format xml:lang="sl">str. 39-46</dc:format><dc:identifier>ISSN:1318-0207</dc:identifier><dc:identifier>COBISSID:22021893</dc:identifier><dc:identifier>URN:URN:NBN:SI:doc-JMRGYATZ</dc:identifier><dc:language>en</dc:language><dc:publisher xml:lang="sl">Slovensko kemijsko društvo</dc:publisher><dcterms:isPartOf xml:lang="sl">Acta chimica slovenica</dcterms:isPartOf><dc:subject xml:lang="sl">analizna kemija</dc:subject><dc:subject xml:lang="sl">kinetika</dc:subject><dc:subject xml:lang="sl">nitroksidni radikali</dc:subject><dc:subject xml:lang="sl">redukcija</dc:subject><dc:subject xml:lang="sl">sečna kislina</dc:subject><dc:subject xml:lang="sl">spektralna analiza</dc:subject><dc:subject xml:lang="sl">superoksidni radikali</dc:subject><dcterms:temporal rdf:resource="1998-2025" /><dc:title xml:lang="sl">The involvement of uric acid in the scavenging of nitroxide radicals by ascorbate|</dc:title><dc:description xml:lang="sl">The reaction kinetics, measured by electron paramagnetic resonance (EPR) was used to study the involvement of uric acid in the reactions of nitroxide radical (TEMPONE) scavenging by ascorbate (PBS, pH 7.4 and T=37 C). In absence of iron ions, the oxygen reoxidation of hydroxylamine was slow and the addition of uric acid not change the observed kinetics. On the other hand, in presence of iron ions the reoxidation starts to recover the nitroxide radical. This reaction rate is strongly enhanced by uric acid, In fact there are two hypotheses, the first ascribes more efficient iron complexes with uric acid, by which the reoxidation increases. Especially the competition between the phosphate and uric acid ligands might be important. However, uric acid could be directly involved in scavenging the hydroxyl radicals, and herewith influence the reaction rate. No scavenging activity of uric acid in UV irradiated aqueous solutions was found. The trapped adducts of hydroxyl andthe superoxide radicals sho the same concetration in presence and absence of uric acid</dc:description><dc:description xml:lang="sl">Raziskali smo vpliv sečne kisline na kinetiko redukcije nitroksidnih radikalovz askorbatom. Uporabili smo metodo metodo elektroparamagnetne resomamce (EPR) in spinski označevalec TEMPON. Reakcije so potekale v PBS oziroma Tris-HCI pufru pri pH 7,4 in T=37 C. V odsotnosti železovih ionov je bila reoksidacija hidroksilamina počasna in dodatek sečne kisline ni povzročil sprememb hitrosti reakcije. V prisotnosti železovih ionov je reoksidacija hitrejša, prisotnost sečne kisline pa bistveno pospeši reoksidacijo hidroksilamina. Dejansko sta tu dve možnosti in sicer, da sečna kislina tvori železov kompleks, ki je bolj aktiven v smislu hitrosti redoks reakcije-reoksidacije kot železovi fosfati, oziroma da sečna kislina mimo tega posega v hitrost reakcije neposredno. Glede na poskus v Tris-HCI pufru, kjer pospeševalnega efekta sečne kisline ni, je prva hipoteza bolj verjetna. To potrjujeta tudi oba poskusa s spinskimi lovilci, kjer ni bilo opaziti vpliva sečne kisline na tvorbo kisikovih radikalov, z vzbujanjem tvorbe kisikovih radikalov s Fentonovo reakcijo, oziroma z obsevanjem z UV žarki</dc:description><edm:type>TEXT</edm:type><dc:type xml:lang="sl">znanstveno časopisje</dc:type><dc:type xml:lang="en">journals</dc:type><dc:type rdf:resource="http://www.wikidata.org/entity/Q361785" /></edm:ProvidedCHO><ore:Aggregation rdf:about="http://www.dlib.si/?URN=URN:NBN:SI:doc-JMRGYATZ"><edm:aggregatedCHO rdf:resource="URN:NBN:SI:doc-JMRGYATZ" /><edm:isShownBy rdf:resource="http://www.dlib.si/stream/URN:NBN:SI:doc-JMRGYATZ/5f735e61-4b24-419c-94ec-b5e1bf34ca25/PDF" /><edm:rights rdf:resource="http://creativecommons.org/licenses/by/4.0/" /><edm:provider>Slovenian National E-content Aggregator</edm:provider><edm:intermediateProvider xml:lang="en">National and University Library of Slovenia</edm:intermediateProvider><edm:dataProvider xml:lang="sl">Slovensko kemijsko društvo</edm:dataProvider><edm:object rdf:resource="http://www.dlib.si/streamdb/URN:NBN:SI:doc-JMRGYATZ/maxi/edm" /><edm:isShownAt rdf:resource="http://www.dlib.si/details/URN:NBN:SI:doc-JMRGYATZ" /></ore:Aggregation></rdf:RDF>