Publication:
Determination of finasteride in the tablet form by liquid chromatography and its analytical method validation

dc.contributor.authorCÜCÜ, AYŞEN
dc.contributor.authorsDemir, H; Cucu, A; Sakarya, S
dc.date.accessioned2022-03-12T17:19:20Z
dc.date.accessioned2026-01-11T14:03:54Z
dc.date.available2022-03-12T17:19:20Z
dc.date.issued2006
dc.description.abstractA quantitative method for finasteride by liquid chromatography (LC) with UV detector, was validated for its new tablet form Dilaprost (R). Analysis was performed using Nova Pak C-18 column at 60 degrees C. Detection was carried out at a wavelength of 210 nm. The best separation for finasteride peak was achieved by isocratic elution with the mobile phase water/acetonitrile/tetrahydrofuran (80/10/10, v/v/v) and flow rate of 2 mL min(-1). The sample volume injected into liquid chromatography system was 15 mu L. Analytical method validation tests were performed. (c) 2005 Elsevier B.V. All rights reserved.
dc.identifier.doi10.1016/j.aca.2005.10.033
dc.identifier.issn0003-2670
dc.identifier.urihttps://hdl.handle.net/11424/228091
dc.identifier.wosWOS:000234963900038
dc.language.isoeng
dc.publisherELSEVIER SCIENCE BV
dc.relation.ispartofANALYTICA CHIMICA ACTA
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectfinasteride
dc.subjectDilaprost (R)
dc.subjectvalidation
dc.subjectRAT
dc.subject5-ALPHA-REDUCTASE
dc.titleDetermination of finasteride in the tablet form by liquid chromatography and its analytical method validation
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage255
oaire.citation.issue1-2
oaire.citation.startPage252
oaire.citation.titleANALYTICA CHIMICA ACTA
oaire.citation.volume557

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