Literature DB >> 2341489

Chemical stability of cefotetan disodium in 5% dextrose and 0.9% sodium chloride injections.

V Das Gupta1, Y Pramar, C Odom, T Zerai, C Bethea.   

Abstract

The chemical stability of cefotetan disodium in 5% dextrose and 0.9% sodium chloride injections has been studied using a stability-indicating high-pressure liquid chromatographic (HPLC) assay method. The drug appears to be relatively unstable at 25 degrees C (expiry time 2 days), compared with at least 41 days at 5 degrees C and at least 60 days at -10 degrees C. Thawing the frozen samples in a microwave (90 s) did not cause any significant decomposition. The manufacturer's recommended expiry time of 4 days at 5 degrees C and at least 7 days at -10 degrees C is very conservative. The HPLC method developed is accurate and precise with a relative percentage standard deviation of 1.7 based on six readings. The method appears to be stability-indicating as the samples decomposed under drastic conditions had almost no drug left and new peaks were observed in the chromatograms.

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Year:  1990        PMID: 2341489     DOI: 10.1111/j.1365-2710.1990.tb00364.x

Source DB:  PubMed          Journal:  J Clin Pharm Ther        ISSN: 0269-4727            Impact factor:   2.512


  1 in total

1.  A simple and sensitive liquid chromatographic technique for the determination of cefotetan disodium in human plasma and its application in a pharmacokinetic study.

Authors:  Yani Liu; Jiangeng Huang; Jinmei Liu; Lin Ma; Yongning Lv; Shaojun Shi
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2012-10-18
  1 in total

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