Hydrolysis of cyclosporin A (CsA) was studied in order to clarify the
still undefined point of attack of the acidic degradation. Among ether
extractable and water-soluble products formed from CsA in HCl, two op
en-chain peptides were isolated by high-performance liquid chromatogra
phy which were identified as the deca- and nonapeptides deriving from
CsA through the hydrolytic cleavage of amino acid residue 11 and both
residues 11 and 10, respectively. Identification was carried out by fa
st atom bombardment tandem mass spectrometry.