High-speed microchip electrophoresis method for the separation of (R,S)-naproxen

Elizabeh Guihen, Anna Marie Hogan, Jeremy D. Glennon

Research output: Contribution to journalArticlepeer-review

Abstract

In this research, a capillary electrophoretic method for the fast enantiomeric resolution of (R,S)-naproxen was investigated. Method development involved variation of applied potential, buffer concentration, buffer pH, and cyclodextrin concentration. The optimum electrophoretic separation conditions were 110 mM sodium acetate run buffer (pH 6.0), 30mM methyl-β-cyclodextrin, 20% (v/v) acetonitrile, 25°C. The total length of capillary was 48 cm, (50 μm I.D.) with ultra violet (UV) detection at 232 nm. Using these conditions, the number of theoretical plates was close to one million (896,000/m). The possibility of achieving a fast chiral separation of (R,S)-naproxen on a microchip of 2.5 cm in length was investigated. Complete enantiomeric resolution of naproxen was achieved in less than 1 min, on this microchip platform, with linear imaging UV detection. This system had the advantage of real-time separation monitoring, so that enantiomeric resolution could be visually observed, and high-speed chiral analysis was realized. The microchip electrophoresis (MCE) separation was compared with the capillary electrophoresis (CE) separation with regards to speed, efficiency, separation platform, and precision. This work highlights the potential of CE and MCE in future chiral separations.

Original languageEnglish
Pages (from-to)292-298
Number of pages7
JournalChirality
Volume21
Issue number2
DOIs
Publication statusPublished - 2009
Externally publishedYes

Keywords

  • (R,S)-naproxen
  • Microchip electrophoresis (MCE)
  • Non-steroidal anti-inflammatory drugs (NSAID)
  • Pharmaceutical analysis

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