静脉给药后肽核酸的药代动力学和组织分布。

B. McMahon, D. Mays, J. Lipsky, J. Stewart, A. Fauq, E. Richelson
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引用次数: 89

摘要

肽核酸(PNAs)是DNA类似物,与互补的核酸序列杂交,具有高亲和力和稳定性。在我们之前的研究中,我们发现,与大鼠神经紧张素受体(rNTR1) mRNA编码区12碱基对(bp)序列互补的PNA,即使腹腔注射PNA (i.p),也能有效阻断大鼠对神经紧张素(NT)的中枢反应。使用一种新的凝胶移位检测方法来检测PNA,我们现在已经使用相同的PNA序列来推导其药代动力学变量及其在大鼠中的组织分布。PNA的分布半衰期为3 +/- 3分钟,消除半衰期为17 +/- 3分钟。该PNA的总血浆清除率和分布体积分别为3.4 +/- 0.9 ml/min x kg和60 +/- 30 ml/kg。给药2小时后,PNA在所有器官中均可检测到,但含量较低,按浓度递减顺序依次为:肾、肝、心、脑和脾。大约90%的PNA剂量在给药24小时后以未改变的母体化合物形式在尿液中恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacokinetics and tissue distribution of a peptide nucleic acid after intravenous administration.
Peptide nucleic acids (PNAs) are DNA analogs that hybridize to complementary nucleic sequences with high affinity and stability. In our previous work, we showed that a PNA complementary to a 12-base pair (bp) sequence of the coding region of the rat neurotensin receptor (rNTR1) mRNA is effective in significantly blocking a rat's central responses to neurotensin (NT), even when the PNA is injected intraperitoneally (i.p.). Using a novel gel shift detection assay to detect PNA, we have now used this same PNA sequence to derive its pharmacokinetic variables and its tissue distribution in the rat. The PNA has a distribution half-life of 3 +/- 3 minutes and an elimination half-life of 17 +/- 3 minutes. The total plasma clearance and volume of distribution of this PNA were 3.4 +/- 0.9 ml/min x kg and 60 +/- 30 ml/kg. Two hours after dosing, the PNA was found at detectable but low levels in all organs examined-in order of decreasing concentration: kidney, liver, heart, brain, and spleen. Approximately 90% of the PNA dose was recovered as unchanged parent compound in the urine 24 hours after administration.
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