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dc.contributor.authorJahangiri, A
dc.contributor.authorAdibkia, K
dc.contributor.authorAsadpour-Zeynali, K
dc.contributor.authorJavadzadeh, Y
dc.contributor.authorHamishehkar, H
dc.contributor.authorBarzegar-Jalali, M
dc.date.accessioned2018-08-26T08:35:05Z
dc.date.available2018-08-26T08:35:05Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52615
dc.description.abstractBackground: Two simple, precise and accurate multivariate calibration methods, partial least square (PLS) and principal component regression (PCR) have been applied for the simultaneous determination and dissolution profile evaluation of atorvastatin (ATV) and ezetimibe (EZT) in their binary mixtures and commercial tablets. Due to the closely overlapping spectral bands of the mentioned drugs, simultaneous determination without previous separation is not possible by conventional spectrophotometric methods. In the proposed methods (PLS and PCR) determination of chemicals was performed by the use of a full-spectrum multivariate calibration method. Methods: The experimental calibration matrix was designed orthogonally with 16 samples composed of different mixtures of both compounds in related mediums. The simultaneous determination of ATV and EZT was accomplished in mixtures through recording the absorption spectra within a range of 210 to 300 nm. Results: The concentration of ATV and EZT were considered in the linear range, between 8 to 14 ?g.ml-1. The specificity of the methods was evaluated by analyzing laboratory prepared mixtures of the mentioned drugs in specific proportions. Conclusion: The applied methods were successfully employed in simultaneous spectrophotometric determination and dissolution profile evaluation of ATV and EZT in their prepared mixtures and pharmaceutical formulation. é 2016 The Authors.
dc.language.isoEnglish
dc.relation.ispartofPharmaceutical Sciences
dc.subjectatorvastatin
dc.subjectezetimibe
dc.subjectArticle
dc.subjectcalibration
dc.subjectchemical analysis
dc.subjectchemical composition
dc.subjectconcentration (parameters)
dc.subjectcontrolled study
dc.subjectdrug formulation
dc.subjectdrug mixture
dc.subjectdrug solubility
dc.subjectdrug structure
dc.subjectpartial least square
dc.subjectprincipal component regression
dc.titleApplication of multivariate calibration methods, in dissolution testing and simultaneous determination of atorvastatin and ezetimibe in their combined solid dosage form
dc.typeArticle
dc.citation.volume22
dc.citation.issue2
dc.citation.spage105
dc.citation.epage111
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.15171/PS.2016.17


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