Biotransformation of sulindac in end-stage renal disease

In normal humans sulindac, a prodrug, undergoes two major biotransformations: irreversible oxidation to the inactive sulfone metabolite and reversible reduction to the pharmacologically active sulfide metabolite. To assess any effect of end-stage renal failure on sulindac biotransformation, six patients were given 200 mg sulindac orally. Plasma was sampled over 24 hours. Protein binding of sulindac and metabolites was determined by equilibrium dialysis. Results were compared with historic controls. AUC(0–12) for sulindac and the sulfone were similar to controls. AUC(0–12) for the sulfide was significantly reduced to 4.85 µg · hr/ml from 13.1 µg · hr/ml (P < 0.02). Protein binding of all three compounds was significantly reduced by renal failure. When corrected for protein binding, the AUC(0–12) for sulindac and the sulfone was twice that of controls whereas that of the sulfide was 42 ng · hr/ml compared with 83 ng · hr/ml in normal individuals (P < 0.001). This suggests that end-stage renal failure impairs the reduction of sulindac to the active sulfide whereas oxidation to the sulfone is intact. Clinical Pharmacology and Therapeutics (1987) 42, 82–88; doi:10.1038/clpt.1987.112