Two novel solvent system compositions for protected synthetic peptide purification by centrifugal partition chromatography

J Chromatogr A. 2014 Apr 11:1337:155-61. doi: 10.1016/j.chroma.2014.02.052. Epub 2014 Feb 28.

Abstract

Protected synthetic peptide intermediates are often hydrophobic and not soluble in most common solvents. They are thus difficult to purify by preparative reversed-phase high-performance liquid chromatography (RP-HPLC), usually used for industrial production. It is then challenging to develop alternative chromatographic purification processes. Support-free liquid-liquid chromatographic techniques, including both hydrostatic (centrifugal partition chromatography or CPC) and hydrodynamic (counter-current chromatography or CCC) devices, are mainly involved in phytochemical studies but have also been applied to synthetic peptide purification. In this framework, two new biphasic solvent system compositions covering a wide range of polarity were developed to overcome solubility problems mentioned above. The new systems composed of heptane/tetrahydrofuran/acetonitrile/dimethylsulfoxide/water and heptane/methyl-tetrahydrofuran/N-methylpyrrolidone/water were efficiently used for the CPC purification of a 39-mer protected exenatide (Byetta®) and a 8-mer protected peptide intermediate of bivalirudin (Angiox®) synthesis. Phase compositions of the different biphasic solvent systems were determined by (1)H nuclear magnetic resonance. Physico-chemical properties including viscosity, density and interfacial tension of these biphasic systems are also described.

Keywords: Biphasic solvent systems; centrifugal partition chromatography (CPC); preparative chromatography; protected peptides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Countercurrent Distribution / methods
  • Exenatide
  • Hirudins / isolation & purification*
  • Magnetic Resonance Spectroscopy
  • Peptide Fragments / isolation & purification*
  • Peptides / isolation & purification*
  • Recombinant Proteins / isolation & purification
  • Solubility
  • Solvents / chemistry*
  • Venoms / isolation & purification*

Substances

  • Hirudins
  • Peptide Fragments
  • Peptides
  • Recombinant Proteins
  • Solvents
  • Venoms
  • Exenatide
  • bivalirudin