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Određivanje nitrata IE-HPLC-UV metodom u moždanim tkivima Wistar pacova trovanih parakvatom

dc.creatorĆurčić-Jovanović, Marijana
dc.creatorĐukić, Mirjana
dc.creatorVasiljević, Ivana
dc.creatorNinković, Milica
dc.creatorJovanović, Marina
dc.date.accessioned2019-09-02T11:12:07Z
dc.date.available2019-09-02T11:12:07Z
dc.date.issued2007
dc.identifier.issn0352-5139
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/1021
dc.description.abstractThis work was a part of an initial study regarding the involvement of reactive nitrogen species (RNS) in paraquat (PQ) neurotoxicity. The nitrate concentration in the vulnerable regions of the brain (cortex, striatum and hippocampus) of Wistar rats was used as a measure of nitric oxide (NO) production or catabolism of the formed RNS. The tissue homogenates were deproteinized with acetonitrile and then centrifuged. Nitrate was measured in filtrated supernatants by simple and rapid isocratic ion-exchange high performance liquid chromatography with UV detection (IE-HPLC-UV) at 214 nm. The mobile phase (pH 8.5) consisted of borate buffer/gluconate concentrate, methanol, acetonitrile and deionized water (2:12:12:74, v/v/v/v), and the flow rate was 1.3 mL/min. Physiological nitrate levels (18.8 ± 6.1 nmol/mg of proteins), as well as a diverse range of nitrate concentrations could be determined with good precision (CV = 2.2 %) and accuracy (recovery of spiked samples was 99 ± 4%) in the brain tissue homogenates. Linearity was achieved in the range of nitrate from 0-80 μM. The retention time of nitrate anion was 5.3 ± 0.3 min. .en
dc.description.abstractPrezentovani rad je deo započete studije o uključenosti reaktivnih vrsta azota (RNS) u neurotoksičnost parakvata (PQ). Sadržaj nitrata u selektivno osetljivim moždanim regijama (cortex, striatum i hippocampus) Wistar pacova može se koristiti kao merilo produkcije azotmonoksida ili katabolizma drugih RNS. Homogenizati moždanog tkiva su najpre deproteinizovani, zatim centrifugirani. Nitrati su određivani u filtriranom supernatantu brzom i jednostavnom izokratskom metodom visoko efikasne tečne hromatografije sa diode-array detekcijom (IE-HPLC-UV) na 214 nm. Korišćena je mobilna faza sastava: boratni pufer/glukonat koncentrat : metanol : acetonitril : dejonizovana voda (2:12:12:74, v/v/v/v), pH 8,5, pri protoku 1,3 mL/min. Širok opseg koncentracija nitrata kao i njihovi fiziološki nivoi (18,8 ± 6,1 nmol/mg proteina) mogu se meriti sa dobrom preciznošću (CV = 2,2%) i tačnošću (recovery opterećenih uzoraka 99 ± 4%) u homogenizatima moždanih tkiva. Linearnost je dobijena u opsegu 0-80 μmol/L nitrata dok je retenciono vreme bilo 5,3 ± 0,3 min. .sr
dc.publisherSrpsko hemijsko društvo, Beograd
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/145010/RS//
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceJournal of the Serbian Chemical Society
dc.subjectnitrateen
dc.subjectIE-HPLC-UVen
dc.subjectbrainen
dc.subjectparaquaten
dc.titleDetermination of nitrate by the IE-HPLC-UV method in the brain tissues of Wistar rats poisoned with paraquaten
dc.titleOdređivanje nitrata IE-HPLC-UV metodom u moždanim tkivima Wistar pacova trovanih parakvatomsr
dc.typearticle
dc.rights.licenseBY-NC-ND
dcterms.abstractЈовановић, Марина; Ћурчић-Јовановић, Маријана; Ђукић, Мирјана; Васиљевић, Ивана; Нинковић, Милица;
dc.citation.volume72
dc.citation.issue4
dc.citation.spage347
dc.citation.epage356
dc.citation.other72(4): 347-356
dc.citation.rankM23
dc.identifier.wos000247047000005
dc.identifier.doi10.2298/JSC0704347C
dc.identifier.scopus2-s2.0-34249780112
dc.identifier.fulltexthttps://farfar.pharmacy.bg.ac.rs//bitstream/id/19/1019.pdf
dc.type.versionpublishedVersion


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