Paper Contents
Abstract
A new simple, accurate, economic, rapid and precise reverse phase high performance liquid chromatographic method has been developed for the validated of Artemether and Lumefantrine, in its pure form as well as in pharmaceutical dosage form. Chromatography was carried out on X bridge C18 (4.6150mm) 5 column using a mixture of Methanol: Phosphate Buffer pH-3.6 (30:70vv) as the mobile phase at a flow rate of 1.0mlmin, the detection was carried out at 260nm. The retention time of the Artemether and Lumefantrine was 2.669, 3.8550.02min respectively. The method produce linear responses in the concentration range of 10-50gml of Artemether and 10-50gml of Lumefantrine. The method precision for the determination of assay was below 2.0%RSD. The method is useful in the quality control of bulk and pharmaceutical formulations.
Copyright
Copyright © 2023 R Vara Laxmi. This is an open access article distributed under the Creative Commons Attribution License.
