Development And Uv-Vis Spectrophotometric Analysis Of An Ease-Of-Use Pediatric Oral Solution Of Dexamethasone For Personalized Therapies

dc.contributor.authorEnes, Duygu
dc.contributor.authorFidan, Bilge Basak
dc.contributor.authorKaplan, Ozan
dc.contributor.authorDogan, Aysegul
dc.contributor.authorAltinoz, Sacide
dc.contributor.authorCelebier, Mustafa
dc.contributor.authorKaynak, Mustafa Sinan
dc.date.accessioned2025-04-21T06:57:06Z
dc.date.issued2024-10-02
dc.description.abstractThe usage of dexamethasone for pediatric applications is a well-known issue. In the present study, we developed an oral dexamethasone solution formulation especially aimed for dose-dependent personalized therapies and having excipients known as not harmful to be safely used in pediatrics. The aim of this study was to prepare an easy-of-use pediatric oral solution of dexamethasone and develop an UV/VIS Spectrophotometric method for the evaluation of the stability and quality control of the developed formulation. The primary source of dexamethasone for preparation of the oral pediatric solution was the dexamethasone one-time injectable solutions. This allowed the formulation to be easily prepared in basic laboratory conditions. Dexamethasone content and stability of the formulation were ensured by quantification using the developed UV/VIS Spectrophotometric method validated based on ICH Q2 (R1) guidelines. Simple, fast, reliable, and validated spectrophotometric analysis of dexamethasone was carried out at 269 nm wavelength and the method was linear in a range of 1.00 to 50.00 mu g mL-1.The developed formulation was stable at 4 degrees C at least for three weeks when protected from daylight. The other stability conditions (ambient temperature and -20 degrees C) were also evaluated for the assays. Although the methodology used in this study contains simple processes which can be easily adapted to basic laboratory conditions, the results were satisfactory to prepare an ease-of-use pediatric oral solution of dexamethasonefor personalized medicine. The validated UV/VIS Spectrophotometric method was selective for the formulation and easily applied for the quality control and stability studies of the samples. Such formulations could be helpful for health professionals in managing real-life corticosteroid treatment application problems especially for pediatrics in hospital pharmacy.
dc.identifier.issn2630-6344
dc.identifier.scopus2-s2.0-85204433651
dc.identifier.urihttps://hdl.handle.net/11727/12883
dc.identifier.wos001315469600039
dc.language.isoen_US
dc.publisherJOURNAL OF RESEARCH IN PHARMACY
dc.subjectDexamethasone
dc.subjectpediatrics
dc.subjectpersonalized medicine
dc.subjectUV-VIS spectroptrophotometry
dc.subjectoral solution
dc.subjectCORTICOSTEROIDS
dc.subjectHEALTH
dc.titleDevelopment And Uv-Vis Spectrophotometric Analysis Of An Ease-Of-Use Pediatric Oral Solution Of Dexamethasone For Personalized Therapies
dc.typeArticle

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