Chemometrics-assisted voltammetric determination of timolol maleate and brimonidine tartrate utilizing a carbon paste electrode modified with iron (III) oxide nanoparticles

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorAbou Al Alamein A.M.
dc.contributor.authorHendawy H.A.M.
dc.contributor.authorElabd N.O.
dc.contributor.otherAnalytical Chemistry Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherCairo University
dc.contributor.otherP.O. Box 11562
dc.contributor.otherCairo
dc.contributor.otherEgypt; National Organization for Drug Control and Research (NODCAR)
dc.contributor.otherP.O. Box 29
dc.contributor.otherCairo
dc.contributor.otherEgypt; Analytical Chemistry Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherMSA University
dc.contributor.otherP.O. Box 2511
dc.contributor.otherGiza
dc.contributor.otherEgypt
dc.date.accessioned2020-01-09T20:40:40Z
dc.date.available2020-01-09T20:40:40Z
dc.date.issued2019
dc.descriptionScopus
dc.description.abstractA carbon paste electrode modified with iron (III) oxide nanoparticles (MCPE) was fabricated for the simultaneous quantitative voltammetric determination of timolol maleate (TM) and brimonidine tartrate (BT) using chemometrics analysis. In this paper, for the first time, a novel voltammetric method was developed for a rapid, sensitive and efficient simultaneous determination of TM and BT in the marketed ophthalmic formulation. This method is based on the incorporation of iron (III) oxide nanoparticles into the carbon paste electrode which improves the characteristics of the electrode and increases its sensitivity. The electrochemical oxidation of the two drugs was established using cyclic voltammetry (CV), differential pulse voltammetry (DPV) and square wave voltammetry (SWV) techniques. DPV and SWV techniques were developed for the quantitative voltammetric determination of TM and BT in their pure forms and pharmaceutical formulations. The method revealed a minimum detectability (LOD) of 1.31 � 10?6 ?g/mL for BT and 1.37 � 10?5 ?g/mL for TM and a limit of quantitation (LOQ) of 3.97 � 10?6 ?g/mL for BT and 4.16 � 10?5 ?g/mL for TM for SWV. Different chemometric methods (PCR and PLS) were tested for the resolution of the overlapped peaks of both compounds and their determination in mixtures. The best results were obtained with the PLS method. The proposed method was validated and compared with the reported HPLC method, revealing the good accuracy, precision and reproducible results of this method. � 2018 Elsevier B.V.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=20922&tip=sid&clean=0
dc.identifier.doihttps://doi.org/10.1016/j.microc.2018.10.042
dc.identifier.doiPubMed ID :
dc.identifier.issn0026265X
dc.identifier.otherhttps://doi.org/10.1016/j.microc.2018.10.042
dc.identifier.otherPubMed ID :
dc.identifier.urihttps://t.ly/X0zDL
dc.language.isoEnglishen_US
dc.publisherElsevier Inc.en_US
dc.relation.ispartofseriesMicrochemical Journal
dc.relation.ispartofseries145
dc.subjectBrimonidine tartrateen_US
dc.subjectChemometricsen_US
dc.subjectTimolol maleateen_US
dc.subjectVoltammetryen_US
dc.titleChemometrics-assisted voltammetric determination of timolol maleate and brimonidine tartrate utilizing a carbon paste electrode modified with iron (III) oxide nanoparticlesen_US
dc.typeArticleen_US
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