In this study, we used solid-phase extraction with Sep-Pak and a liqui
d-liquid extraction with methylene chloride as two primary methods of
extracting FK506 from plasma. The extracts were either analyzed direct
ly by enzyme-linked immunosorbent assay (ELISA) or subjected to high-p
erformance liquid chromatography (HPLC) separation and different fract
ions were analyzed by ELISA. Serial blood samples were obtained from f
our kidney transplant patients and four patients who underwent liver t
ransplantation, from day 1 until day 30-35 posttransplantation. There
was no significant difference in the FK506 plasma concentration as mea
sured by all four methods in normal transplant patients. However, in l
iver transplant patients, the solid-phase extraction method gave highe
r FK506 concentrations than the methylene chloride extraction during t
he early postoperative period. The concentrations measured after methy
lene chloride extraction were higher than that after HPLC-ELISA. This
higher FK506 concentration measured by direct ELISA could be attribute
d to possible cross-reacting metabolites that were present in the plas
ma of patients with abnormal liver functions. Once liver function retu
rns to normal, all four methods give identical plasma concentrations f
or FK506.