肖淑华, 魏广力, 陆榕, 刘昌孝, 王锋鹏. 溴泰君在大鼠的组织分布和排泄J. 药学学报, 2005, 40(5): 453-456.
引用本文: 肖淑华, 魏广力, 陆榕, 刘昌孝, 王锋鹏. 溴泰君在大鼠的组织分布和排泄J. 药学学报, 2005, 40(5): 453-456.
XIAO Shu-hua, WEI Guang-li, LU Rong, LIU Chang-xiao, WANG Feng-peng. Tissue distribution and excretion of bromotetrandrine in ratsJ. Acta Pharmaceutica Sinica, 2005, 40(5): 453-456.
Citation: XIAO Shu-hua, WEI Guang-li, LU Rong, LIU Chang-xiao, WANG Feng-peng. Tissue distribution and excretion of bromotetrandrine in ratsJ. Acta Pharmaceutica Sinica, 2005, 40(5): 453-456.

溴泰君在大鼠的组织分布和排泄

Tissue distribution and excretion of bromotetrandrine in rats

  • 摘要: 目的研究溴泰君(W198)在大鼠的组织分布和排泄,为临床试验提供依据。方法用HPLC紫外检测方法测定大鼠iv W198后生物样品中的药物含量。结果大鼠iv W198 20 mg·kg-1后组织的药物含量远高于相同时间的血清药物浓度。药物主要分布在肺,其次在肾、心、肝等组织,大部分组织的药物含量于给药后0.25 h最高,给药后2 h显著下降,至24 h均缓慢下降;大鼠iv W198 20 mg·kg-1后从尿、粪(0-96 h)和胆汁(0-24 h)中排泄的原型药物分别占给药总量的0.150%,2.1%和0.063%。结论W198主要分布于肺组织中。从尿、粪和胆汁中排泄的原型药物很少。

     

    Abstract: AimTo study the tissue distribution and excretion of bromotetrandrine (W198) in rats.MethodsThe concentrations of W198 in biological samples were determined by an HPLC method with UV detection.ResultsAfter a single iv dose of 20 mg·kg-1 W198 in rats, the parent drug concentrations in tissues were higher than those in blood at the same time.Parent drug was mainly distributed in lung, kidney, heart and liver, the peak levels were attained at 025 h and decreasing at 2 h after dosing in most tissues.After a single iv dose of 20 mg·kg-1 W198 in rats, the excretion of the parent drug in urine, feces and bile amounted to 0150%, 21% and 0063% of the dose, respectively.ConclusionW198 was mostly distributed in lung.The parent drug excretion was less than 3% via urine, feces and bile.

     

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