Desmosine (DES) and isodesmosine (IDE) were separated and quantitated
by a simple and sensitive capillary zone electrophoretic (CZE) method,
using hydrostatic injection and direct UV detection at 254 or 185 nm.
Two different electrophoretic mobilities for the two isoforms were ob
served in 90 mM phosphoric acid pH 2.2. The presence of a mixture of a
mino acids in the sample did not affect the separation of DES and IDE.
The method was successfully used to quantitate the amounts of DES and
IDE in elastin hydrolysates.