Simultaneous Pharmacokinetic Analysis of Nitrate and its Reduced Metabolite, Nitrite, Following Ingestion of Inorganic Nitrate in a Mixed Patient Population.

PURPOSE

The pharmacokinetic properties of plasma NO and its reduced metabolite, NO, have been separately described, but there has been no reported attempt to simultaneously model their pharmacokinetics following NO ingestion. This report describes development of such a model from retrospective analyses of concentrations largely obtained from primary endpoint efficacy trials.

METHODS

Linear and non-linear mixed effects analyses were used to statistically define concentration dependency on time, dose, as well as patient and study variables, and to integrate NO and NO concentrations from studies conducted at different times, locations, patient groups, and several studies in which sample range was limited to a few hours. Published pharmacokinetic studies for both substances were used to supplement model development.

RESULTS

A population pharmacokinetic model relating NO and NO concentrations was developed. The model incorporated endogenous levels of the two entities, and determined these were not influenced by exogenous NO delivery. Covariate analysis revealed intersubject variability in NO exposure was partially described by body weight differences influencing volume of distribution. The model was applied to visualize exposure versus response (muscle contraction performance) in individual patients.

CONCLUSIONS

Extension of the present first-generation model, to ultimately optimize NO dose versus pharmacological effects, is warranted.