A Comparative Study of Newly Developed HPLC-DAD and UHPLC-UV Assays for the Determination of Posaconazole in Bulk Powder and Suspension Dosage Form. (2nd September 2014)

• Record Type: Journal Article
• Authors: Hamdy, Dalia A.; Belal, Tarek S.
• Other Names: Esteve-Romero Josep Academic Editor.
• Is Part Of: Journal of analytical methods in chemistry. Volume 2014(2014)
• Publication Date: 2014-09-02
• Subjects: Chemistry, Analytic -- Periodicals; Chemistry, Analytic -- Technique -- Periodicals; 543.05
• DOI: 10.1155/2014/241035
• Languages: English
• ISSNs: 2090-8865

Abstract

Abstract : Objective . To develop and compare HPLC-DAD and UHPLC-UV assays for the quantitation of posaconazole in bulk powder and suspension dosage form. Methods . Posaconazole linearity range was 5–50 μ g/mL for both assays. For HPLC-DAD assay, samples were injected through Zorbax SB-C18 (4.6 × 250 mm, 5 μ m) column. The gradient elution composed of the mobile phase acetonitrile: 15 mM potassium dihydrogen orthophosphate (30 : 70 to 80 : 20, linear over 7 minutes) pumped at 1.5 mL/min. For UHPLC-UV assay, samples were injected through Kinetex-C18 (2.1 × 50 mm, 1.3 μ m) column. The mobile phase composed of acetonitrile: 15 mM potassium dihydrogen orthophosphate (45 : 55) pumped isocratically at 0.4 mL/min. Detection wavelength was 262 nm in both methods. Results . The run time was 11 and 3 minutes for HPLC-DAD and UHPLC-UV assays, respectively. Both assays were linear (r 2 > 0.999 ) with CV% and % error of the mean <3%. Limits of detection and quantitation were 0.82 and 2.73 μ g/mL for HPLC-DAD and 1.04 and 3.16 μ g/mL for UHPLC-UV, respectively. The methods quantitated PSZ in suspension dosage form with no observable interferences. Conclusions . Both assays were proven sensitive and selective according to ICH guidelines. UHPLC-UV assay exhibited some economic and chromatographic separation superiority.