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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2007, Vol. 12 ›› Issue (1): 93-97.

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Pharmacokinetic study of rh-IFNα2a in mice and rats after intravenous and intramuscular administration

LU Li, CUI Ming-xia, WANG Li, ZHANG Bao-lai, WU Yong-jie   

  1. Pharmacology Research Institute of Pharmacy College, Lanzhou University, Pharmacology Lab of Gansu Province Key Laboratory of Preclinircal study for new drugs, Lanzhou 730000, Gansu, China
  • Received:2006-10-16 Revised:2006-10-23 Online:2007-01-26 Published:2020-10-26

Abstract: AIM: To study pharmacokinetic property of rh-IFNα2a after intravenous (i.v.) and intramuscular (i.m.) injection to mice and rats. METHODS: Double antibody sandwich ELISA analysis was used for testing drug concentration in serum, urine, bile and tissues after i.v.and i.m.administration of rh-IFNα2a in mice and rats.Pharmacokinetic parameters were calculated by DAS software.Immunohistochemistry technique was also adopted to evaluate its distribution characters. RESULTS: Pharmacokinetic model of rh-IFNα2a after i.v.and i.m. was consistent with two-compartment and one-compartment open model respectively, both submitting to first-order kinetic elimination.Rh-IFNα2a was predominantly distributed in kidney and lung tissue.The total drug accumulative excretion quantity in urine was 0.121 %of the administered after rh-IFNα2a 8.19 μg/kg i.v.into mice. The total drug accumulative excretion quantity in bile was 0.247 %of the administered after rh-IFNα2a 4.10 μg/kg i.v.into rats. CONCLUSION: Pharmacokinetic models after i.v.and i.m.rh-IFNα2a are two-compartment open model and one-compartment open model, respectively, both with first-order kinetic elimination.

Key words: interferon, pharmacokinetics, enzymelinked immunosorbent assay

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