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dc.contributor.authorÖnal, Armağan
dc.contributor.authorErgin Kızılçay, Gamze
dc.contributor.authorToker, Sıdıka
dc.contributor.authorÇağlar Andaç, Sena
dc.date.accessioned2021-03-04T09:19:56Z
dc.date.available2021-03-04T09:19:56Z
dc.identifier.citationErgin Kızılçay G., Çağlar Andaç S., Önal A., Toker S., "Spectrophotometric determination of 3-hydroxy-3-methylglutaryl coenzyme-A reductase inhibitors in pharmaceutical preparations", Turkish Journal of Chemistry, cilt.37, ss.171-181, 2013
dc.identifier.issn1300-0527
dc.identifier.othervv_1032021
dc.identifier.otherav_67b802c6-4fe8-4f69-beae-6f543023ad09
dc.identifier.urihttp://hdl.handle.net/20.500.12627/71978
dc.identifier.urihttps://avesis.istanbul.edu.tr/api/publication/67b802c6-4fe8-4f69-beae-6f543023ad09/file
dc.description.abstractSimple and accurate spectrophotometric methods are presented for the determination of five 3-hydroxy-3- methylglutaryl coenzyme-A (HMG-CoA) reductase inhibitors (statins), namely atorvastatin, fluvastatin, pitavastatin, rosuvastatin, and simvastatin, in pharmaceutical preparations. The methods are based on the reaction of drugs as n-electron donor with 7,7,8,8-tetracyanoquinodimethane as π-acceptors to give highly colored complex species. All variables were studied in order to optimize the reaction conditions. Beer’s law was obeyed in the concentration ranges 4–20 μg mL −1 , 4–12 μg mL −1 , 0.8–2.4 μg mL −1 , 4–14 μg mL −1 , and 2.5–20 μg mL −1 for atorvastatin, fluvastatin, pitavastatin, rosuvastatin, and simvastatin, respectively. The proposed methods were successfully applied to the pharmaceutical preparations without any interference from excipients.
dc.language.isotur
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.titleSpectrophotometric determination of 3-hydroxy-3-methylglutaryl coenzyme-A reductase inhibitors in pharmaceutical preparations
dc.typeMakale
dc.relation.journalTurkish Journal of Chemistry
dc.contributor.departmentİstanbul Üniversitesi , Eczacılık Fakültesi , Temel Eczacılık Bilimleri Bölümü
dc.identifier.volume37
dc.identifier.startpage171
dc.identifier.endpage181
dc.contributor.firstauthorID2213710


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