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静脉注射后肽核酸的药代动力学和组织分布

Pharmacokinetics and tissue distribution of a peptide nucleic acid after intravenous administration.

作者信息

McMahon Beth M, Mays Dennis, Lipsky James, Stewart Jennifer A, Fauq Abdul, Richelson Elliott

机构信息

Laboratory of Neuropsychopharmacology, Mayo Foundation for Medical and Educational Research, Jacksonville, FL 32224, USA.

出版信息

Antisense Nucleic Acid Drug Dev. 2002 Apr;12(2):65-70. doi: 10.1089/108729002760070803.

Abstract

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.

摘要

肽核酸(PNA)是一种DNA类似物,能与互补核酸序列以高亲和力和稳定性杂交。在我们之前的研究中,我们发现一种与大鼠神经降压素受体(rNTR1)mRNA编码区12个碱基对(bp)序列互补的PNA,即使通过腹腔注射(i.p.),也能有效显著阻断大鼠对神经降压素(NT)的中枢反应。我们现在使用一种新型凝胶迁移检测法来检测PNA,利用相同的PNA序列得出其在大鼠体内的药代动力学变量及其组织分布。该PNA的分布半衰期为3±3分钟,消除半衰期为17±3分钟。这种PNA的总血浆清除率和分布容积分别为3.4±0.9 ml/min·kg和60±30 ml/kg。给药两小时后,在所有检测的器官中均发现了可检测到但含量较低的PNA,浓度由高到低依次为:肾脏、肝脏、心脏、大脑和脾脏。给药24小时后,约90%的PNA剂量以未变化的母体化合物形式在尿液中回收。

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