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Article Navigation >  Journal of Pharmaceutical Practice and Service  > 1999  >  (2): 95-96

Wang Yong, Ma Jun. Pharmacokinetics of m-nifedipine in rabbits after intravenous injection[J]. Journal of Pharmaceutical Practice and Service, 1999, (2): 95-96.
Citation: Wang Yong, Ma Jun. Pharmacokinetics of m-nifedipine in rabbits after intravenous injection[J]. Journal of Pharmaceutical Practice and Service, 1999, (2): 95-96.
shu

Pharmacokinetics of m-nifedipine in rabbits after intravenous injection

  • 1.

    Department of Pharmacy, NO.208 Hospital of PLA, Jining 012000

  • 2.

  • Received Date: 1998-08-26
  • OBJECTIVE To study the dose effects on pharmacokinetics of m-Nif. METHODS 15 rabbits were divided into 3 groups receiving iv m-Ni f 05,1,and 2 mg/kg Plasma levels of m-Nif were determined with HPLC method. RESULTS The concentration-time data were fitted with 2-compartment model.The parameters were after iv l mg/kg:Vd=0.37L/kg,Tα/2=6.4min,Tβ/2=84.1min,AUC=94.1mg·min/L,CL=0.65L/(kg·h).No statistically significant diference was found in C1 and Tβ/2 between 3 dose groups.AUC (standardized to body weight)was correlated with doses. CONCLUSION m-Nif was distributed widely and eliminated at a fairly rapid rate in the rabbits.No dose-dependent pharmacokinetics was found after iv m-Nif 0.52mg/kg.
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    沈阳化工大学材料科学与工程学院 沈阳 110142

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Pharmacokinetics of m-nifedipine in rabbits after intravenous injection

  • 1. Department of Pharmacy, NO.208 Hospital of PLA, Jining 012000
  • 2. 
  • Received Date: 1998-08-26

Abstract: OBJECTIVE To study the dose effects on pharmacokinetics of m-Nif. METHODS 15 rabbits were divided into 3 groups receiving iv m-Ni f 05,1,and 2 mg/kg Plasma levels of m-Nif were determined with HPLC method. RESULTS The concentration-time data were fitted with 2-compartment model.The parameters were after iv l mg/kg:Vd=0.37L/kg,Tα/2=6.4min,Tβ/2=84.1min,AUC=94.1mg·min/L,CL=0.65L/(kg·h).No statistically significant diference was found in C1 and Tβ/2 between 3 dose groups.AUC (standardized to body weight)was correlated with doses. CONCLUSION m-Nif was distributed widely and eliminated at a fairly rapid rate in the rabbits.No dose-dependent pharmacokinetics was found after iv m-Nif 0.52mg/kg.

Wang Yong, Ma Jun. Pharmacokinetics of m-nifedipine in rabbits after intravenous injection[J]. Journal of Pharmaceutical Practice and Service, 1999, (2): 95-96.
Citation: Wang Yong, Ma Jun. Pharmacokinetics of m-nifedipine in rabbits after intravenous injection[J]. Journal of Pharmaceutical Practice and Service, 1999, (2): 95-96.
shu

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