Title of article :
Development and Validation of a Reversed-phase HPLC Method for Assay of the Decapeptide Cetrorelix Acetate in Bulk and Pharmaceutical Dosage Forms
Author/Authors :
Hooshfar, Shirin Department of Pharmaceutics - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran , Mortazavi, Alireza Department of Pharmaceutics - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran , Piryaei, Mohammad Medical Genetics Department - Faculty of Medicine - Shahid Beheshti University of Medical Sciences, Tehran , Ramandi Darzi, Hossein Medical Genetics Department - Faculty of Medicine - Shahid Beheshti University of Medical Sciences, Tehran , Shahsavari, Nahid Department of Clinical Pharmacy - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran , Kobarfard, Farzad Department of Medicinal Chemistry - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran - Central Research Laboratories - Shahid Beheshti University of Medical Sciences, Tehran - Phytochemistry Research Center - Shahid Beheshti University of Medical Sciences, Tehran
Pages :
8
From page :
43
To page :
50
Abstract :
A gradient reversed-phase high performance liquid chromatography (HPLC) method was developed for the assay of cetrorelix acetate, a synthetic decapeptide with gonadotropin-releasing hormone (GnRH) antagonistic activity used in infertility treatment. The HPLC method, which is used to determine cetrorelix in bulk and pharmaceutical dosage forms, was validated per ICH guidelines. The chromatographic separation was achieved on a C18 reversed-phase column using acetonitrile, water and trifluoroacetic acid (TFA) as mobile phase and wavelength was set at 275 nm. The calibration curve was linear (r2 = 0.999) over cetrorelix concentrations ranging from 62.50 to 12.50 μg/mL (n = 6). The limits of detection (LOD) and quantification (LOQ) were calculated from the peak-to-noise ratio as 15.6 and 62.5 μg/mL, respectively. The method had an accuracy of > 97% and intra- and inter-day RSD of < 0.3% and < 1.6%, respectively and was validated with excellent specificity, sensitivity, and stability. The validated method was successfully applied for determination of cetrorelix in bulk and pharmaceutical dosage forms.
Keywords :
Cetrorelix acetate , HPLC , Assay , UV detection , Formulation
Journal title :
Astroparticle Physics
Serial Year :
2014
Record number :
2416251
Link To Document :
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