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Updated: Jul 9, 2026

Quantification of the Immunosuppressant Tacrolimus on Dried Blood Spots Using LC-MS/MS
Published on: November 8, 2015
Oral tacrolimus bioavailability is increased after right split liver transplantation
1Department of General, Visceral, and Vascular Surgery, Friedrich-Schiller-University, Jena, Germany.
Objective:
Tacrolimus (Tac) is mainly metabolized in the liver. The aim of this trial was to analyze Tac bioavailability after partial liver transplantation.
Patients And Methods:
A total of 33 patients after right split liver grafting (n=8 living related, LRLT; n=8 cadaver split, CS) or full-size liver transplantation (n=17, FS) were included in this trial. All of them received Tac perorally with an initial dose of 2x5 mg/d. Dose adjustment was performed according to the Tac trough level (T0) with an initial target T0 levels of 12 to 15 ng/mL.
Results:
The time to reach target T0 levels tended to be lower (P=.05) in the split liver groups (LRLT: 2.8+/-1.6 days; CS: 2.1+/-0.9 days; FS: 4.5+/-3.2 days). In addition, mean Tac dose to maintain the target T0 level was significantly decreased (P=.01) in the split liver cohorts (LRLT: 5.8+/-1.1 mg/d; CS: 5.5+/-2.5 mg/d; FS: 9.8+/-3.9 mg/d). Only graft weight/standard liver volume ratio (r=.566, P=.02) and graft weight/body weight ratio (r=.709, P=.002) showed significant correlations with Tac maintenance doses in the split liver group.
Conclusions:
Peroral Tac bioavailability was significantly higher after partial liver transplantation using the right hepatic lobe compared with full-size transplants. The volume of the split liver graft highly correlated with Tac maintenance therapy and should be used to calculate the most appropriate initial posttransplantation Tac dose.
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