What is it about?
This paper reports a validated high-performance liquid chromatography method which is rapid, highly specific, and accurate for determination of cefazolin sodium in injectable pharmaceutical formulations. Separation was carried out using a Hibar® µBondapak® C18 column with a mobile phase consisting of an acetonitrile to monobasic sodium phosphate buffer ratio of 17:83 and a flow rate of 1.0 mL per minute, and monitoring at a wavelength of 254 nm. The calibration curve was linear, with a correlati
Featured Image
Read the Original
This page is a summary of: Novel HPLC method for quantitative determination of cefazolin sodium in pharmaceutical formulations, Research and Reports in Medicinal Chemistry, August 2013, Taylor & Francis,
DOI: 10.2147/rrmc.s43254.
You can read the full text:
Resources
Contributors
The following have contributed to this page
