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A Pharmacokinetic and Tissue Distribution Study of a Palladium Labeled MicroparticleFormulation (Pd-AI-700)Following Intravenous Administration in Rats

机译:大鼠静脉内给药后钯标记的微粒制剂(Pd -AI-700)的药代动力学和组织分布研究

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Pharmacokinetics and tissuedistribution of [Pd]-AI-700 were determinedfollowing intravenous administration in rats.Pd was cleared from blood with a ca. 50-85% decline in concentration during a fiveminute interval immediately post-dose. At1440 minutes post-dose, 52 to 72% of thedose was recovered from organs of thereticuloendothelial system.
机译:药代动力学和组织 确定[Pd] -AI-700的分布 在大鼠中静脉内给药之后。 大约从血液中清除了钯。 50- 五个月内注意力下降了85% 用药后立即间隔一分钟。在 给药后1440分钟,占剂量的52%至72% 从器官的器官中回收剂量 网状内皮系统。

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