Determination of Carbidopa, Levodopa, and Droxidopa by high-performance liquid chromatography–tandem mass spectrometry

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Modern treatments o Parkinson’s disease include the use of carbidopa and droxidopa along with levodopa that demonstrates the necessity for their binary and simultaneous determination in pharmaceutical tablets and biological matrices. This study presents a rapid, accurate, and precise method for the simultaneous determination of these analytes by liquid chromatography–tandem mass spectrometry method for the first time. Accordingly, performances of two types of analytical columns, namely, octadecylsilane and hydrophilic interaction liquid chromatographic columns, were tested and better resolution was obtained with the former. The pH of aqueous mobile phase (0.5% formic acid) was adjusted to 2.3 to ensure the analytes were in molecular form. Calibration graphs were obtained using multiple reaction mode and detection limits were in the region from 0.002 to 0.007 μM for both columns. The method developed was applied for quality control samples and tablets and satisfactory recovery values from 100 to 106% were obtained. © 2018 Taylor & Francis.

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AlanDeğerDil
dc.contributor.authorÖzdokur, Kemal Volkan
dc.contributor.authorEngin, Esra
dc.contributor.authorYengin, Çiğdem
dc.contributor.authorErtaş, Hasan
dc.contributor.authorErtaş, F. Nil
dc.date.accessioned2026-10-18T20:29:09.535593463Z
dc.date.available2026-10-18T20:29:09.535593463Z
dc.date.issued2018
dc.description.abstractModern treatments o Parkinson’s disease include the use of carbidopa and droxidopa along with levodopa that demonstrates the necessity for their binary and simultaneous determination in pharmaceutical tablets and biological matrices. This study presents a rapid, accurate, and precise method for the simultaneous determination of these analytes by liquid chromatography–tandem mass spectrometry method for the first time. Accordingly, performances of two types of analytical columns, namely, octadecylsilane and hydrophilic interaction liquid chromatographic columns, were tested and better resolution was obtained with the former. The pH of aqueous mobile phase (0.5% formic acid) was adjusted to 2.3 to ensure the analytes were in molecular form. Calibration graphs were obtained using multiple reaction mode and detection limits were in the region from 0.002 to 0.007 μM for both columns. The method developed was applied for quality control samples and tablets and satisfactory recovery values from 100 to 106% were obtained. © 2018 Taylor & Francis.
dc.description.sponsorshipThis project was supported by TUBITAK with project number 114 Z 153.
dc.identifier.doi10.1080/00032719.2017.1316283
dc.identifier.eissn1532-236X
dc.identifier.endpage82
dc.identifier.issn0003-2719
dc.identifier.issue1-2
dc.identifier.scopus2-s2.0-85032181705
dc.identifier.startpage73
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14364
dc.identifier.volume51
dc.identifier.wosWOS:000416519900006
dc.language.isoen
dc.publisherTaylor and Francis Inc.
dc.relation.ispartofAnalytical Letters
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCarbidopa
dc.subjectDroxidopa
dc.subjectHigh-performance liquid chromatography–tandem mass spectrometry (HPLCMS)
dc.subjectHydrophilic interaction liquid chromatography (HILIC)
dc.subjectLevodopa
dc.titleDetermination of Carbidopa, Levodopa, and Droxidopa by high-performance liquid chromatography–tandem mass spectrometry
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus21
rdl.citation.wos20
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)