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Development and validation of LC-MS/MS method for the determination of cyproheptadine in several pharmaceutical syrup formulations. Journal of pharmaceutical and biomedical analysis [J Pharm Biomed Anal] Journal article

 
TitleDevelopment and validation of LC-MS/MS method for the determination of cyproheptadine in several pharmaceutical syrup formulations.
Author(s)Feás X, Ye L, Hosseini SV, Fente CA, Cepeda A 
InstitutionDepartment of Analytical Chemistry, Nutrition and Bromatology, Veterinary Faculty, University of Santiago de Compostela, 27002 Lugo, Galiza, Spain; Department of Pure and Applied Biochemistry, Chemical Center, Lund University, 221 00 Lund, Sweden.
SourceJ Pharm Biomed Anal 2009 Jun 12.
AbstractA rapid and sensitive liquid chromatographic-tandem mass spectrometric (LC-MS/MS) method was developed and validated for the qualitative and quantitative assay of cyproheptadine (CP) in pharmaceutical samples. Diphenylpyraline hydrochloride (DPP) was used as an internal standard (IS). Two multiple reaction-monitoring (MRM) transitions for each analyte were observed: 288.1/96.1 and 288.1/191.2 for CP and 282.1/167.2 and 282.1/116.3 for DPP. The retention time of the drug was 7.29min. The analytical method was successfully validated for linearity (1-100ng/ml), intra-day precision, inter-day precision, and accuracy. The limit of detection (LOD) and limit of quantification (LOQ) were 0.86 and 0.98ng/ml, respectively. The proposed method was applied to analyse the cyproheptadine content from seven different syrup formulations.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID19574011
  
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