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Pharm Res. 2014 Dec;31(12):3265-73. doi: 10.1007/s11095-014-1416-1. Epub 2014 May 23.

Interspecies pharmacokinetic modeling of subcutaneous absorption of rituximab in mice and rats.

Author information

1
Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, 160 Frelinghuysen Road, Piscataway, New Jersey, 08854, USA, lkagan@pharmacy.rutgers.edu.

Abstract

PURPOSE:

To investigate the effect of dose level and anatomical site of injection on the pharmacokinetics of rituximab in mice, and to evaluate the utility of a pharmacokinetic model for describing interspecies differences in subcutaneous absorption between mice and rats.

METHODS:

Rituximab serum concentrations were measured following intravenous and subcutaneous administration at the back and abdomen of mice. Several approaches were compared for scaling model parameters from estimated values in rats.

RESULTS:

The bioavailability of rituximab following subcutaneous injection was inversely related to the dose level and was dependent on the site of injection in mice. The overall rate of absorption was faster in mice as compared to rats. Subcutaneous absorption profiles were well described using the proposed structural model, in which the total receptor concentration, the affinity of rituximab to the receptor, and the degradation rate constant were assumed to be species independent.

CONCLUSIONS:

Subcutaneous absorption processes show similar trends in rats and mice, although the magnitude differs between species. A mathematical model that combines the absorption of free and bound antibody with presystemic degradation successfully captured rituximab pharmacokinetics in both species, and approaches for sharing and scaling parameters between species were identified.

PMID:
24852895
PMCID:
PMC4469501
DOI:
10.1007/s11095-014-1416-1
[Indexed for MEDLINE]
Free PMC Article

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