Impurity profile study of repaglinide

J Pharm Biomed Anal. 2003 Jul 14;32(3):461-7. doi: 10.1016/s0731-7085(03)00216-4.

Abstract

Three unknown impurities and a byproduct in repaglinide bulk drug at levels below 0.1% (ranging from 0.05 to 0.1%) were detected by a simple isocratic reversed-phase high performance liquid chromatography (HPLC) method. These impurities were isolated from crude sample of repaglinide using reversed-phase preparative high performance liquid chromatography. Based on the spectroscopic data (IR, NMR and MS) the structures of these impurities (I, II and IV) and byproduct (III) were characterised as 4-carboxymethyl-2-ethoxy-benzoic acid (I), 4-cyclohexylaminocarbamoylmethyl-2-ethoxy-benzoic acid (II), 1-cyclohexyl-3-[3-methyl-1-(2-piperidin-1-yl-phenyl)-butyl]-urea (IV) and 1,3-dicyclohexyl urea (III), respectively. Their synthesis and formation is discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbamates / analysis*
  • Chromatography, High Pressure Liquid
  • Drug Contamination
  • Hypoglycemic Agents / analysis*
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Piperidines / analysis*
  • Spectroscopy, Fourier Transform Infrared

Substances

  • Carbamates
  • Hypoglycemic Agents
  • Piperidines
  • repaglinide