Literature DB >> 15533692

Determination and in-process control of zolpidem synthesis by high-performance liquid chromatography.

L Laviana1, C Mangas, F Fernández-Marí, M Bayod, D Blanco.   

Abstract

A high-performance liquid chromatographic assay with diode-array detection has been developed for the in-process control of zolpidem synthesis and for the analysis of the drug and its synthetic intermediates. The separation uses a 4.6mm i.d. reversed-phase Kromasil C(18) (150 mm) column, 5 microm particle size with a gradient elution mode of acetonitrile and 0.02 M NH(4)OAc (adjusted to pH 8.0) as the mobile phase (flow rate 1.0 mlmin(-1)). The analysis is performed in 12 min. The method is simple, rapid and highly specific.

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Year:  2004        PMID: 15533692     DOI: 10.1016/j.jpba.2004.08.025

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


  2 in total

1.  Spectrophotometric methods for determination of zolpidem tartrate in tablet formulation.

Authors:  Rajiv Chomwal; Amit Kumar; Anju Goyal
Journal:  J Pharm Bioallied Sci       Date:  2010-10

2.  Development and Validation of a Stability-Indicating Capillary Electrophoresis Method for the Determination of Zolpidem Tartrate in Tablet Dosage Form with Positive Confirmation using 2D- and 3D-DAD Fingerprints.

Authors:  Khaldun M Al Azzam; Lee Kam Yit; Bahruddin Saad; Hassan Shaibah
Journal:  Sci Pharm       Date:  2014-02-27
  2 in total

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