Literature DB >> 15925231

Determination of desloratadine in drug substance and pharmaceutical preparations by liquid chromatography.

Meiling Qi1, Peng Wang, Yingshu Geng.   

Abstract

A simple and selective LC method is described for the determination of desloratadine in drug substance and pharmaceutical preparations. Chromatographic separation was achieved on a Diamonsil BDS C18 column using a mobile phase of a mixture of methanol, 0.03 mol/l heptanesulphonic acid sodium and glacial acetic acid (70:30:4, v/v) at a flow rate of 1.0 ml/min with detection at 247 nm. The developed method was validated in terms of selectivity, linearity, limit of quantitation, precision, accuracy and solution stability. The proposed LC method achieved satisfactory resolution between desloratadine and loratadine possibly present in desloratadine drug substance and other impurities in the mother liquor of the synthetic process. It can be used for the synthetic process control and determination of desloratadine in drug substance and pharmaceutical preparations.

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Year:  2005        PMID: 15925231     DOI: 10.1016/j.jpba.2005.01.003

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  2 in total

1.  A new validated liquid chromatographic method for the determination of loratadine and its impurities.

Authors:  Gajjela Ramulu; Yalavarthi Ravindra Kumar; Krishnamurthy Vyas; Mulukutla V Suryanarayana; Khagga Mukkanti
Journal:  Sci Pharm       Date:  2011-02-12

2.  A Validated Stability-Indicating RP-UPLC Method for Simultaneous Determination of Desloratadine and Sodium Benzoate in Oral Liquid Pharmaceutical Formulations.

Authors:  Navneet Kumar; Dhanaraj Sangeetha; Pingili Sunil Reddy; Lakkireddy Prakash
Journal:  Sci Pharm       Date:  2011-12-12
  2 in total

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