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Pharmacokinetics and splenic accumulation of N‐acetylamino‐3‐chloro‐N‐(2‐diethylamino‐ethyl) benzamide after a single administration to rats
Author(s) -
Hua Jianyi,
Sheng Yezhou,
Olin Magnus,
Pero Ronald,
Edvardsen Klaus
Publication year - 2004
Publication title -
biopharmaceutics and drug disposition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.419
H-Index - 58
eISSN - 1099-081X
pISSN - 0142-2782
DOI - 10.1002/bdd.414
Subject(s) - pharmacokinetics , benzamide , cmax , bioavailability , pharmacology , oral administration , chemistry , spleen , lymphocyte , absorption (acoustics) , half life , distribution (mathematics) , kidney , endocrinology , medicine , stereochemistry , mathematical analysis , physics , mathematics , acoustics
The purpose of this study was to measure the pharmacokinetics and tissue accumulation of N‐acetylamino‐3‐chloro‐N‐(2‐diethylamino‐ethyl) benzamide (NACPA) after oral or intravenous administration at a single dose of 25 mg/kg to female W/Fu rats. The serum pharmacokinetics of NACPA were characterized by rapid absorption, distribution and elimination. However, in comparison with its parent compound, 4‐amino‐3‐chloro‐N‐(2‐diethylamino‐ethyl) benzamide (3‐CPA), NACPA displayed a higher C max (mean±SD, 201±21 vs 33.6±0.5 nmol/ml, p <0.05), and a longer elimination half‐life (50±0.8 vs 36.6±1.1 min, p <0.05) following intravenous administration. Bioavailability of NACPA was significantly greater than that of 3‐CPA (50% compared with 14%, p <0.05). The tissue accumulation of NACPA was generally higher than that of 3‐CPA. NACPA was deposited at higher concentrations in the spleen than in the kidney and liver. Cellular pharmacokinetics indicated that NACPA accumulated more readily in lymphocyte related cells than in liver related cells. Furthermore, incubation of human peripheral lymphocytes with NACPA resulted in inhibition of lymphocyte proliferation, INF‐ γ production and chemotaxis. All these results suggest that NACPA may be a good candidate drug for oral administration for immune modulation. Copyright © 2004 John Wiley & Sons, Ltd.