Extending the scope of enantiomer separation by capillary supercritical fluid chromatography on immobilized polysiloxane-anchored permethyl-β-cyclodextrin (Chirasil-Dex)

✍ Scribed by Jung, Martin ;Schurig, Volker

• Publisher: John Wiley and Sons
• Year: 1993
• Tongue: English
• Weight: 596 KB
• Volume: 16
• Category: Article
• ISSN: 0935-6304
• DOI: 10.1002/jhrc.1240160403

✦ Synopsis

Abstract

Immobilized polysiloxane‐anchored permethyl‐β‐cyclodextrin (Chirasil‐Dex) with a cyclodextrin content of approximately 30 % by weight, previously employed as a versatile chiral stationary phase for the separation of enantiomers by GC, has been used for the separation of enantiomers by capillary supercritical fluid chromatography (SFC). A considerable number of racemates could be resolved, e.g. aromatic alcohols, amino alcohols (TFA derivatives), and underivatized acids. Many pharmaceutical compounds were among those analyzed, including several NSAIDs (e.g. ibuprofen and ketoprofen), a steroidal drug (nor‐gestrel), a barbiturate (hexobarbital), and others.

Among the racemates resolved were many which cannot be analyzed by GC owing to low volatility or decomposition at elevated temperatures. For two racemates, analysis temperature and mobile phase density were systematically varied to give constant analysis times or capacity factors k. Low temperatures (ca 60 °C) yielded the best separation in term of separation factor, α, or resolution, R~s~, even though higher densities had to be used. In comparison with GC, capillary SFC was able to furnish higher separation factors and similar resolution. The applicability of capillary SFC for the analysis of mixtures of cyclodextrin derivatives, e.g. those used in the synthesis of Chirasil‐Dex, was, furthermore, demonstrated.