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Influence of various combinations of specific antibody dose and affinity on tissue imipramine redistribution
Author(s) -
Ragusi Corinne,
Boschi Gabrielle,
Risède Patricia,
Rips Richard,
Harrison Kenneth,
Scherrmann JeanMichel
Publication year - 1998
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0702033
Subject(s) - chemistry , antibody , imipramine , pharmacokinetics , polyclonal antibodies , medicine , immunology , pathology , alternative medicine
1 This study was designed to evaluate the distribution kinetics of imipramine (Imip) in the brain and the main peripheral organs (heart, kidney, liver and lung) of rats, and to establish the relationship between the redistribution of Imip from these tissues and the immunoreactive capacity (dose and affinity) of anti‐TCA IgG. 2 [ 3 H]‐Imip (1 nmol kg −1 body weight) was injected intravenously 6 min before the i.v. injection of antibodies. At this time, the concentrations of Imip and its main metabolites in plasma were determined. The radioactivity measured corresponded to 91.7% Imip, indicating that the pharmacokinetics reflected essentially Imip. Plasma and tissue Imip contents were measured over the interval 1 to 90 min in control and in treated rats. The antibodies used were a murine monoclonal IgG 1 (Ka=3.8 10 7 M −1 ) at an IgG 1 / Imip molar ratio of 1000 (IgG 1 1000), and a sheep polyclonal IgG (TAb, Ka=1.3 10 10 M −1 ) at IgG/Imip molar ratios of 1, 10 and 100 (TAb1, TAb10 and TAb100). 3 The anti‐TCA IgG increased the plasma [ 3 H]‐Imip concentrations: the AUC 1→60 min for [ 3 H]‐Imip were 4 (IgG 1 1000), 9 (TAb1), 33.9 (TAb10) and 41.4 (TAb100) times higher in the treated groups than in the controls. The opposite effect occurred in the brain, heart and lungs, with large, rapid decreases in Imip. The increase in plasma Imip and the decrease in tissue Imip depended on the immunoreactive capacity (NKa) of the antibody, where N=molar concentration of IgG binding sites and Ka=IgG affinity constant. Maximal plasma and tissue redistribution occurred when NKa=33.8×10 4 . 4 Imip redistribution can be controlled using various doses or affinities of specific antibodies, and the resulting rapid, extensive Imip redistribution from the main target organs could be very promising for TCA detoxification.British Journal of Pharmacology (1998) 125 , 35–40; doi: 10.1038/sj.bjp.0702033