The design and use of a solid-phase injector for open tubular column s
upercritical fluid chromatography (SFC) are reported. For sample intro
duction, a liquid sample was loaded on a platinum wire. After the solv
ent had evaporated, the wire was inserted into, and sealed in, the inj
ector. The chromatographic run was started by introducing the supercri
tical mobile phase into the injector. Absolute and relative peak area
reproducibilities, as well as retention time reproducibility, of the i
njection method were evaluated. The relative standard deviations (% RS
Ds) of absolute and relative peak areas were 2.0-4.5 and 0.4-1.8%, res
pectively, for both 1- and 2-mul injections. Larger deviations were ob
served for compounds that had high vapor pressures. The % RSDs of rete
ntion times from six subsequent injections were 0.04-0.06.