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Development of a New, Fully Validated LC-MS/MS Method for the Analysisof Flibanserin in Pharmaceutical Preparations and Comparison of theChromatographic Performance with Six Stationary Phase Types

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dc.contributor.authorGeven, Aysun
dc.contributor.authorÖZCAN, SANİYE
dc.contributor.authorLEVENT, SERKAN
dc.contributor.authorCAN, NAFİZ ÖNCÜ
dc.contributor.orcid0000-0001-5436-7519
dc.contributor.orcid0000-0002-5492-0457
dc.contributor.orcid0000-0003-3692-163X
dc.contributor.orcid0000-0003-0280-518X
dc.date.accessioned2025-11-13T18:47:38Z
dc.date.issued2023-07-27
dc.identifier.doihttps://doi.org/10.2174/1573411019666230726121218
dc.identifier.endpage549
dc.identifier.issn1573-4110
dc.identifier.issue7
dc.identifier.openalexW4385310793
dc.identifier.startpage541
dc.identifier.urihttps://hdl.handle.net/11421/10641
dc.identifier.urihttps://doi.org/10.2174/1573411019666230726121218
dc.identifier.volume19
dc.language.isoen
dc.relation.ispartofCurrent Analytical Chemistry
dc.rightsrestrictedAccess
dc.subjectChromatography
dc.subjectChemistry
dc.subjectAmmonium formate
dc.subjectFood and drug administration
dc.subjectDetection limit
dc.subjectAcetonitrile
dc.subjectPharmacology
dc.subjectMedicine
dc.subject.sdg3
dc.titleDevelopment of a New, Fully Validated LC-MS/MS Method for the Analysisof Flibanserin in Pharmaceutical Preparations and Comparison of theChromatographic Performance with Six Stationary Phase Types
dc.typeArticle
dspace.entity.typePublication
local.authorid.openalexA5012333467
local.authorid.openalexA5067792682
local.authorid.openalexA5075534569
local.authorid.openalexA5001553522

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