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dc.creatorOsmanović Omerdić, Ehlimana
dc.creatorAlagić-Džambić, Larisa
dc.creatorKrstić, Marko
dc.creatorPašić-Kulenović, Maja
dc.creatorOdović, Jadranka
dc.creatorVasiljević, Dragana
dc.date.accessioned2020-08-05T07:48:11Z
dc.date.available2020-08-05T07:48:11Z
dc.date.issued2020
dc.identifier.issn2076-3417
dc.identifier.urihttp://farfar.pharmacy.bg.ac.rs/handle/123456789/3637
dc.description.abstractSolid dispersions were prepared via a solvent evaporation method, employing ethanol (96%, v/v) as solvent, with three different polymers as carrier: povidone, copovidone, and poloxamer 407. Previously developed reversed-phase HPLC (RP-HPLC) methods were modified and used for the simultaneous determination of acetylsalicylic acid and clopidogrel bisulfate and after release from solid dispersions. Chromatography was carried out on a C-18 column, with a mobile phase of acetonitrile-methanol-phosphate buffer pH 3.0, UV detection at 240 nm, and a run time of 6 min. The method was validated according to International Conference of Harmonisation guidelines and validation included specificity, accuracy, precision, linearity, robustness, limit of detection (LOD), and limit of quantification (LOQ). The method is specific for determination of acetylsalicylic acid and clopidogrel bisulfate. The linearity was provided in the concentration range 0.0275-0.1375 mg/mL for acetylsalicylic acid and 0.0200-0.1000 mg/mL for clopidogrel bisulfate, with a correlation coefficient (R2 value) of 0.9999 for both active pharmaceutical ingredients (APIs). Accuracy was confirmed by calculated recoveries for acetylsalicylic acid (98.6-101.0%) and clopidogrel bisulfate (100.0-101.6%). The intra-day and the inter-day precision-calculated relative standard deviations are less than 1%, which indicates high precision of the method. The limits of detection and quantification for acetylsalicylic acid were 0.0004 and 0.0012 mg/mL, and for clopidogrel bisulfate 0.0002 mg/mL and 0.0007 mg/mL, respectively. Small variations in chromatographic conditions did not significantly affect qualitative and quantitative system responses, which proved robustness of method. The proposed RP-HPLC method was applied for simultaneous determination of clopidogrel bisulfate and acetylsalicylic acid from solid dispersions.
dc.publisherMDPI AG
dc.rightsopenAccess
dc.sourceApplied Sciences (Switzerland)
dc.subjectAcetylsalicylic acid
dc.subjectClopidogrel bisulfate
dc.subjectDissolution
dc.subjectRP-HPLC
dc.subjectSolid dispersion
dc.subjectValidation
dc.titleIn vitro dissolution study of acetylsalicylic acid and clopidogrel bisulfate solid dispersions: Validation of the RP-HPLC method for simultaneous analysis
dc.typearticle
dc.rights.licenseBY
dcterms.abstractКрстић, Марко; Пашић-Куленовић, Маја; Aлагић-Джамбић, Лариса; Османовић Омердић, Ехлимана; Одовић, Јадранка; Васиљевић, Драгана;
dc.citation.volume10
dc.citation.issue14
dc.identifier.wos000554858500001
dc.identifier.doi10.3390/app10144792
dc.identifier.scopus2-s2.0-85088659853
dc.identifier.fulltexthttp://farfar.pharmacy.bg.ac.rs/bitstream/id/7898/In_Vitro_Dissolution_pub_2020.pdf
dc.type.versionpublishedVersion


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