Supercritical fluid chromatographic resolution of water soluble isomeric carboxyl/amine terminated peptides facilitated via mobile phase water and ion pair formation

• Published in: Journal of Chromatography A 2012-04, Vol.1233, p.85-90
• Main Authors: Patel, M.A., Riley, F., Ashraf-Khorassani, M., Taylor, L.T.
• Format: Article
• Language: English
• Subjects: additives; amino acids; ammonium acetate; Evaporative light scattering; ingredients; Isomers; light scattering; Mass spectrometry; organic salts; Peptides; silica; sulfonates; Supercritical fluid chromatography
• ISSN: 0021-9673
• DOI: 10.1016/j.chroma.2012.02.024

► Isomers of linear decapeptide salts have been separated via packed column SFC. ► Uncapped peptides are separated via bare silica and H2O/MeOH-modified CO2. ► Capped peptide salts are separated via amine-bonded silica without water. ► Separated peptide isomers are detected via mass spectrometry and light scattering. ► HILIC-like retention may operate with hydrated hydroxylated stationary phases. Both analytical scale and preparative scale packed column supercritical fluid chromatography (SFC) have found widespread applicability for chiral separations of multiple polar pharmaceutical candidates. However, SFC is rapidly becoming an achiral technique. More specifically, ion pair SFC is finding greater utility for separation of ionic analytes such as amine salts and organic sulfonates. The key to this success is, in part, the incorporation of additives such as trifluoroacetic acid and ammonium acetate into the mobile phase in association with a wide variety of both bonded silica stationary phases and high purity bare silica. Ion pairing SFC coupled with evaporative light scattering detection and mass spectrometric detection is presented here for the separation of water soluble, uncapped, isomeric peptide pairs that differ in amino acid arrangement. The separation is best achieved on either diol-bonded silica or bare silica with 1–5% (w/w) water as a significant ingredient in the mobile phase. Nitrogenous stationary phases such as 2-ethylpyridine, which had been very successful for the separation of capped peptides failed to yield the desired separation regardless of the mobile phase composition. A HILIC type retention mechanism is postulated for the separation of both isomeric uncapped peptide pairs.