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63Ni-NiCl2在大鼠体内的药代动力学及其组织残留
引用本文:李湛,王颢,吴王锁. 63Ni-NiCl2在大鼠体内的药代动力学及其组织残留[J]. 药学学报, 2008, 43(2): 224-226
作者姓名:李湛  王颢  吴王锁
作者单位:1. 兰州大学核科学与技术学院,甘肃,兰州,730000
2. 兰州大学基础医学院,甘肃,兰州,730000
摘    要:
镍是动物体必需的微量元素,参与核酸和蛋白质的代谢、激素的调节过程,具有刺激生血、促进红细胞再生的功能[1],与激素、蛋白质和脂类的代谢也密切相关.国内相关研究较少,尤其使用同位素标记法研究更少.

关 键 词:63Ni-NiCl2  吸收  药物残留
文章编号:0513-4870(2008)02-0224-03
收稿时间:2007-08-12
修稿时间:2007-08-12

Pharmacokinetic parameter and residua of 63Ni-NiCl2 in rat
LI Zhan,WANG Hao,WU Wang-suo. Pharmacokinetic parameter and residua of 63Ni-NiCl2 in rat[J]. Acta pharmaceutica Sinica, 2008, 43(2): 224-226
Authors:LI Zhan  WANG Hao  WU Wang-suo
Affiliation:School of Nuclear Science and Technology, Lanzhou 730000, China.
Abstract:
Absorption distribution and excretion of 63Ni-NiCl2, administered orally to rats were studied by using liquid scintillation counting method. It was observed that the concentration-time curves in blood fitted the two compartment model of pharmacokinetics, Ka=6.18 h(-1), T(1/2)alpha =0.79 h, T(1/2)beta=40.68 h, CL =0.42 mL kg(-1) h(-1), Tmax =0.53 h, Cmax=24,987.75 min(-1) mL(-1), and Vd=0.016 L kg(-1). After rats were treated by 63Ni-NiCl2 for 15 days, in 22 tissues tested, the contents of 63Ni-NiCl2 in hair, hypothalamus, hypophysis, pancreas, small and large intestines were higher, and the residua of 63Ni-NiCl2 was not discovered in liver, kidney and heart. Radioactivity eliminated was 83.27% by urine and feces, 54.86% by urine, 28.41% by feces.
Keywords:~63 Ni-NiCl_2  absorption  residual medicine
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