Downloads: 115
Research Paper | Chemistry | India | Volume 3 Issue 6, June 2014
Development and Validation New Analytical Methods of Levofloxacin in IV Infusions by UV-Visible spectrophotometric Methods and Determine Assay; % Purity and Stability in Three Marketed Brands
Swapna.G [2] | Deepika.G
Abstract: The present study was undertaken to develop and validate a simple; accurate; precise; reproducible and cost effective UV-Visible spectrophotometric method for the estimation of levofloxacin in bulk and pharmaceutical formulation in three different Brands of cipla lkem; pdpl throught the experiment the solvent used for uv method was water and the absorption spectra was carried out at 288nm and forvisible method reagent used is 2; 4 DNP in methanol and determination carried out at 510 nm. The concentration range is 2-10g/ml. The method was shown linear in the mentioned concentrations with correlation coefficient of R20.9999. The %purityof levofloxacin is 97.4 %-115.2 %. The percent relative standard deviation (RSD %) of method precision and intermediate prescision is
Keywords: Levofloxacin, uv, visible, Assay, Purity, Stability
Edition: Volume 3 Issue 6, June 2014,
Pages: 960 - 963
Similar Articles with Keyword 'uv'
Downloads: 53
Research Paper, Chemistry, Nigeria, Volume 2 Issue 3, March 2013
Pages: 457 - 459Selenium Content in some Brands of Bottled Beer Marketed in Makurdi Town Benue State, Nigeria
A. D. Oklo | R. Sha'Ato | K. Asemave [3] | C.Mkurzurum
Downloads: 134
Research Paper, Chemistry, Libya, Volume 6 Issue 10, October 2017
Pages: 494 - 497The Effect of pH and Ionic Strength on the Bulk and Interfacial Properties of Starches
Fateh Eltaboni | Abedelqader Imragaa | Hamida Altajury | Hana Alshelmany | Nora Omar | Ranya Ali