Literature DB >> 6491963

Determination of sodium levothyroxine in bulk, tablet, and injection formulations by high-performance liquid chromatography.

J F Brower, D Y Toler, J C Reepmeyer.   

Abstract

Sodium levothyroxine was determined in bulk drugs, tablets, and injections by high-performance liquid chromatography (HPLC). Levothyroxine was separated from excipients and impurities on a 10-microns cyanoalkyl column using an acetonitrile-water-phosphoric acid mobile phase. The HPLC method is shown to be linear, accurate, and precise, and the results obtained by the HPLC and USP XX methods are compared.

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Year:  1984        PMID: 6491963     DOI: 10.1002/jps.2600730937

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  2 in total

1.  Kinetics of degradation of levothyroxine in aqueous solution and in solid state.

Authors:  C M Won
Journal:  Pharm Res       Date:  1992-01       Impact factor: 4.200

2.  Development and application of a validated HPLC method for the analysis of dissolution samples of levothyroxine sodium drug products.

Authors:  J W Collier; R B Shah; A R Bryant; M J Habib; M A Khan; P J Faustino
Journal:  J Pharm Biomed Anal       Date:  2010-10-13       Impact factor: 3.935

  2 in total

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