Determination of Ophthalmic Drug Proparacaine Using Multi-walled Carbon Nanotube Paste Electrode by Square Wave Stripping Voltammetry

dc.authoridinam, onur/0000-0002-4726-1190
dc.authoridDemir, Ersin/0000-0001-9180-0609
dc.authorscopusid55910480000
dc.authorscopusid57200525596
dc.authorscopusid6602858808
dc.authorwosidinam, onur/Q-3994-2017
dc.authorwosidDemir, Ersin/V-6633-2019
dc.contributor.authorDemir, Ersin
dc.contributor.authorInam, Onur
dc.contributor.authorInam, Recai
dc.date.accessioned2024-05-25T11:19:28Z
dc.date.available2024-05-25T11:19:28Z
dc.date.issued2018
dc.departmentOkan Universityen_US
dc.department-temp[Demir, Ersin] Okan Univ, Fac Engn, Dept Food Engn, TR-34959 Istanbul, Turkey; [Inam, Onur] Hacettepe Univ, Fac Med, Dept Ophthalmol, TR-06230 Ankara, Turkey; [Inam, Recai] Gazi Univ, Fac Sci, Dept Chem, TR-06500 Ankara, Turkeyen_US
dc.descriptioninam, onur/0000-0002-4726-1190; Demir, Ersin/0000-0001-9180-0609en_US
dc.description.abstractProparacaine, one of the most common local anesthetics to facilitate diagnosis and treatment of eye diseases, was assayed by square wave voltammetry using a paste electrode prepared with carbon nanotubes. In cyclic voltammetric studies, proparacaine has exhibited a single irreversible anodic peak at around + 900 mV vs. Ag/AgCl in pH 6.0 Britton-Robinson buffer solution. It was suggested that the peak had appeared due to the oxidation of the NH2 group on the proparacaine molecule. Prior to the determination of the proparacaine by square wave stripping voltammetry (SWSV) on the fabricated multi-walled carbon nanotube paste electrode (MWCNTPE), the accumulation potential (E-acc), accumulation time (r.c), pulse amplitude (Delta E), step potential (Delta E-s) and frequency (f) parameters were optimized. The peak currents plotted in the range of 0.5 - 12.5 mg/L proparacaine exhibited two linear sections with a detection limit of 0.11 mg/L. The results for the determination of proparacaine on a pharmaceutical local anesthetic (Alcaine) showed that relative standard deviation (RSD) and relative error (RE) were 4.1 and 2.0%, respectively. Selectivity has also been investigated and results showed recoveries of 5.0 mg/L proparacaine in the presence of 5.0 mg/L dopamine, ascorbic acid and uric acid as 106.9 +/- 0.8, 99.9 +/- 1.2 and 94.1 +/- 0.7, respectively.en_US
dc.identifier.citation14
dc.identifier.doi10.2116/analsci.17P589
dc.identifier.endpage776en_US
dc.identifier.issn0910-6340
dc.identifier.issn1348-2246
dc.identifier.issue7en_US
dc.identifier.pmid29998957
dc.identifier.scopus2-s2.0-85049638377
dc.identifier.scopusqualityQ3
dc.identifier.startpage771en_US
dc.identifier.urihttps://doi.org/10.2116/analsci.17P589
dc.identifier.urihttps://hdl.handle.net/20.500.14517/421
dc.identifier.volume34en_US
dc.identifier.wosWOS:000440769400004
dc.identifier.wosqualityQ4
dc.language.isoen
dc.publisherJapan Soc Analytical Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectProparacaineen_US
dc.subjectophthalmic drugen_US
dc.subjectvoltammetryen_US
dc.subjectcarbon nanotube paste electrodeen_US
dc.subjectdeterminationen_US
dc.titleDetermination of Ophthalmic Drug Proparacaine Using Multi-walled Carbon Nanotube Paste Electrode by Square Wave Stripping Voltammetryen_US
dc.typeArticleen_US
dspace.entity.typePublication

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