Pakistan Science Abstracts
Article details & metrics
No Detail Found!!
A RP-HPLC method for the assay of Cefpirome and its application in drug-metal interaction studies.
Author(s):
1. M. Saeed Arayne: Department of Chemistry, University of Karachi, Karachi, Pakistan
2. M. Nawaz: Department of Chemistry, University of Karachi, Karachi, Pakistan
3. Najma Sultana: Research Institute of Pharmaceutical Sciences, Department of Pliarmaceutical Chemistry, Faculty of Pharmacy, University of Karachi, Pakistan
Abstract:
An accurate, sensitive and least time consuming RP-HPLC method for the estimation of cefpirome in the presence of essential and trace metal has been developed and validated. Cefpirome was eluted from a B144A, OD-5-100, C18 (150 x 4.6 mm) column at room temperature with a mobile phase consisting of MeOH:H2O (15:85, % v/v) at a flow rate of 1 ml/minute, while UV detection was performed at 265 nm. The detection limit of cefpirome was 10 ng. Drug metal interaction studies were carried out at 37oC to monitor the complexation of drug with metal ions. These studies were beneficial to determine the drug in therapeutic concentrations inside human body as well as its complexation with metal cations. The metals essential to human body like Mg(II), Ca(ll), Cr(Il), Mn(II), Fe(III), Co(ll), Ni(II), Cu(II), Zn(ll) & Cd(II) were in the form of chlorides. The carboxylic group of the dehydrothiazine ring has more binding capacity relative to other group that augments the drug complexes with essential and trace elements. The established HPLC method is rapid, accurate, and selective, because of its sensitivity and reproducibility. The order of complexation was ferric > chromium > copper > nickel > cadmium > zinc > magnesium > manganese > calcium > cobalt.
Page(s): 39-44
DOI: DOI not available
Published: Journal: Pakistan Journal of Pharmaceutical Sciences, Volume: 19, Issue: 1, Year: 2006
Keywords:
Keywords are not available for this article.
References:
References are not available for this document.
Citations
Citations are not available for this document.
0

Citations

0

Downloads

11

Views