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PHARMACOKINETICS OF HABUTOBIN IN RABBITS

机译:兔habutobin的药代动力学

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Following the administration of habutobin, the fibrinogen level in the circulating blood of the rabbits decreased. These results showed that the activity of habutobin was retained in vivo. The plasma level of habutobin was determined by a ELISA-double sandwich method. The pharmacokinetics of habutobin from Trimeresurus flavoviridis venom was studied in rabbits following i.v. administration of 50 mu g kg(-1) of habutobin. The time course of the plasma concentration of habutobin fitted a two-compartment open model. The half-life of the distribution phase was 4.43 +/- 1.28 min and that of the elimination phase was 50.42 +/- 7.89 min. The area under the plasma concentration-time curve (AUG) was 38.69 +/- 6.68 mu g min ml(-1). The total body clearance was 3.82 +/- 1.08 mi min(-1). When the steady state was reached, the concentration ratio of habutobin in the tissue (C-t) to that in the plasma (C-c), C-t:C-c was 0.47:1. These findings suggest that relatively little habutobin tended to remain in the tissue. [References: 16]
机译:施用habutobin后,兔子循环血液中的纤维蛋白原水平降低。这些结果表明,habutobin的活性在体内得以保留。血红蛋白的血浆水平通过ELISA-双夹心法测定。静脉内注射后,在兔体内研究了来自Trimeresurus flavoviridis毒液的habutobin的药代动力学。施用50μg kg(-1)的habutobin。血红蛋白血浆浓度随时间的变化符合两室开放模型。分布相的半衰期为4.43 +/- 1.28min,消除相的半衰期为50.42 +/- 7.89min。血浆浓度-时间曲线(AUG)下的面积为38.69 +/- 6.68μgmin ml(-1)。全身清除率为3.82 +/- 1.08英里/分钟(-1)。当达到稳态时,组织(C-t)与血浆(C-c)中habutobin的浓度比C-t:C-c为0.47:1。这些发现表明相对较少的habutobin倾向于保留在组织中。 [参考:16]

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