The quantitation of artemether in both pharmaceutical raw material and injections was carried out by high performance liquid chromatography (HPLC) with ultraviolet detection. A Zorbax C18 column (150 x 4.6 mm; 5 μm), at 30 °C, and a mobile phase composed of acetonitrile and water (70:30), at a flow rate of 1ml/min, were used. The detection wavelength was 216 nm and the injection volume was 20 μL. The method proved to be linear (r 2=0.9999), precise (RSD < 20% for intra-day and inter-day precision), accurate and selective regarding possible impurities and excipients of the samples. The detection and quantitation limits were 8 μg/mL and 25 μg/mL, respectively. The artemether content obtained in the raw material analysis was 99.26% and in the injections, 102.08%. The optimized and validated method may be successfully employed to perform routine quality control analyses.
CITATION STYLE
César, I. D. C., & Pianetti, G. A. (2009). Quantitation of artemether in pharmaceutical raw material and injections by high performance liquid chromatography. Brazilian Journal of Pharmaceutical Sciences, 45(4), 737–742. https://doi.org/10.1590/S1984-82502009000400018
Mendeley helps you to discover research relevant for your work.