Determination of metoprolol and felodipine in binary mixture using chemometric-assisted spectrophotometric and high-performance liquid chromatographic-UV methods

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorSalem H.
dc.contributor.authorAbdallah O.M.
dc.contributor.otherAnalytical Chemistry Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherMinia University
dc.contributor.otherMinia
dc.contributor.otherEgypt; Analytical Chemistry Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherAl-Azhar University
dc.contributor.otherCairo
dc.contributor.otherEgypt; Analytical Chemistry Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherMSA University
dc.contributor.otherCairo
dc.contributor.otherEgypt
dc.date.accessioned2020-01-25T19:58:35Z
dc.date.available2020-01-25T19:58:35Z
dc.date.issued2007
dc.descriptionScopus
dc.description.abstractFour methods were developed for simultaneous determination of metoprolol and felodipine without previous separation. In the first method both drugs were determined using first derivative UV spectrophotometry, with zero crossing measurement at 222 and 235 nm for metoprolol and felodipine, respectively. The second method depends on first derivative of the ratios spectra by measurements of the amplitudes at 250.1 nm for metoprolol and 224.3 nm for felodipine. Calibration graphs are established in the range of 20-150 ?g/ml and 10-60 ?g/ml for metoprolol and felodipine, respectively. The third method describes the use of multivariate spectrophotometric calibration for the simultaneous determination of the analyzed binary mixture where the resolution is accomplished by using partial least squares (PLS) regression analysis. Although the components show high degree of spectral overlap, they are simultaneously determined with high accuracy and without interference of pharmaceutical dosage form excipients. A comparison with the related multivariate method of classicial least squares (CLS) analysis is done showing less relative results due to severe spectral overlap of the studied drugs. In the fourth method (HPLC), a reversed-phase column and a mobile phase of methanol:water:acetonitrile (70:22:8 v/v/v/) at 0.9 ml/ min flow rate is used to separate both drugs and UV detection at 260 nm. Good linearities are obtained in concentration range of 0.15-15 ?g/ml for metoprolol and 0.03-5 ?g/ml for felodipine. All the proposed methods are extensively validated. They have the advantage of being economic and time saving. All the described methods can be readily utilized for the analysis of pharmaceutical formulations, the fourth method (HPLC) is successfully applied for the analysis of both drugs in human serum samples. The results obtained by adopting the proposed methods are statistically analyzed and compared with those obtained by reported methods. � 2007 Science Publications.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=6400153122&tip=sid&clean=0
dc.identifier.doihttps://doi.org/10.3844/ajassp.2007.709.717
dc.identifier.doiPubMed ID :
dc.identifier.issn15469239
dc.identifier.otherhttps://doi.org/10.3844/ajassp.2007.709.717
dc.identifier.otherPubMed ID :
dc.identifier.urihttps://t.ly/Wepj9
dc.language.isoEnglishen_US
dc.publisherScience Publicationsen_US
dc.relation.ispartofseriesAmerican Journal of Applied Sciences
dc.relation.ispartofseries4
dc.subjectFelodipineen_US
dc.subjectFirst derivative spectrophotometryen_US
dc.subjectHPLCen_US
dc.subjectHuman serumen_US
dc.subjectMetoprololen_US
dc.subjectMultivariateen_US
dc.subjectPharmaceuticalsen_US
dc.subjectRatio derivative spectrophotometryen_US
dc.titleDetermination of metoprolol and felodipine in binary mixture using chemometric-assisted spectrophotometric and high-performance liquid chromatographic-UV methodsen_US
dc.typeArticleen_US
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