Pharmacokinetics of Stable Caesium after Single Administration of Caesium Chloride in Japanese Black Cattle

Chiaki Shimaoka, T. Kakizaki, Seiichi Wada, Yoshinori Tanaka, T. Abe, M. Natsuhori
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Abstract

Pharmacokinetic (PK) parameters of stable caesium (SCs) were determined in adult Japanese Black Cattle (JBC, n=20). They were divided into two groups, i.e, intravenous (IV) and oral (PO) administration groups, and each of them was administered 133 CsCl solution (20 mg/kg b.w.). SCs in biological samples was measured by ICP-MS, and their concentration-time courses were monitored for 182 days. The PK parameters determined in plasma and blood in each group were as follows (mean±SD); area under the concentration-time curve (AUC;µg/L · h): 0.54±0.06 (IVp), 0.42±0.05 (POp), 0.87±0.11 (IVb), and 0.71±0.33 (POb), mean residence time (MRT; day); 20.9±3.2 (IVp), 19.3±2.9 (POp), 24.7±3.6 (IVb), and 23.6±5.2 (POb), bioavailability (F%); 82±29 and 83±38, clearance (CL; mL/min/kg): 0.46±0.05 (IVp), 0.49±0.06 (POp), 0.29±0.04 (IVb), and 0.31±0.08 (POb), and distribution volume (Vd; L/kg) was 3.3 (Vdp) and 4.4 (Vdb). The biological half-life of the terminal elimination phase (T1/2) was estimated to be approximately 30 days. The urine recovery for the dose was 28±6 (IV) and 28±8 (PO), and the fecal recovery was 85±21 (IV) and 122±42% (PO). The time course via both routes of administration showed similar biphasic distribution and elimination profile in any biological samples and elucidated by compartment analysis with consideration of background level. Based on the PK parameters, elimination profile of radioactive caesium (RCs) from the JBC kept long in the RCs contaminated area can be explained.
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日本黑牛单次施用氯化铯后稳定铯的药动学研究
测定了稳定铯(SCs)在成年日本黑牛(JBC, n=20)体内的药代动力学参数。将小鼠分为静脉(IV)和口服(PO)两组,每组分别给予CsCl溶液133 (20 mg/kg b.w)。采用ICP-MS法测定生物样品中的SCs,并监测其浓度-时间过程,持续182天。各组血浆和血液中PK参数测定结果如下(mean±SD);浓度-时间曲线下面积(AUC;µg/L·h): 0.54±0.06 (IVp)、0.42±0.05 (POp)、0.87±0.11 (IVb)、0.71±0.33 (POb);天);20.9±3.2 (IVp), 19.3±2.9(流行),24.7±3.6 (IVb)司长委任,和23.6±5.2 (POb),生物利用度(F %);82±29和83±38,间隙(CL;mL/min/kg)分别为0.46±0.05 (IVp)、0.49±0.06 (POp)、0.29±0.04 (IVb)、0.31±0.08 (POb),分布体积(Vd;L/kg)分别为3.3 (Vdp)和4.4 (Vdb)。最终消除期(T1/2)的生物半衰期估计约为30天。给药后尿液回收率分别为28±6 (IV)和28±8 (PO),粪便回收率分别为85±21 (IV)和122±42% (PO)。两种给药途径的时间过程在任何生物样本中都显示出相似的双相分布和消除特征,并通过考虑背景水平的室室分析加以阐明。基于PK参数,可以解释JBC中放射性铯(RCs)在RCs污染区停留时间较长的消除情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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