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抗癌药物[(14)C]洛莫司汀在雄性大鼠体内的代谢情况。

Metabolic disposition of the anti-cancer agent [(14)C]laromustine in male rats.

作者信息

Nassar Ala F, Wisnewski Adam, King Ivan

机构信息

Department of Internal Medicine, School of Medicine, Yale University , New Haven, CT , USA .

出版信息

Xenobiotica. 2015;45(8):711-21. doi: 10.3109/00498254.2015.1016475. Epub 2015 Mar 23.

Abstract

1. Laromustine (VNP40101M, also known as Cloretazine) is a novel sulfonylhydrazine alkylating (anticancer) agent. This article describes the use of quantitative whole-body autoradiography (QWBA) and mass balance to study the tissue distribution, the excretion mass balance and pharmacokinetics after intravenous administration of [(14)C]VNP40101M to rats. A single 10 mg/kg IV bolus dose of [(14)C]VNP40101M was given to rats. 2. The recovery of radioactivity from the Group 1 animals over a 7-day period was an average of 92.1% of the administered dose, which was accounted for in the excreta and carcass. Most of the radioactivity was eliminated within 48 h via urine (48%), with less excreted in feces (5%) and expired air accounted for (11%). The plasma half-life of [(14)C]laromustine was approximately 62 min and the peak plasma concentration (Cmax) averaged 8.3 μg/mL. 3. The QWBA study indicated that the drug-derived radioactivity was widely distributed to tissues through 7 days post-dose after a single 10 mg/kg IV bolus dose of [(14)C]VNP40101M to male pigmented Long-Evans rats. The maximum concentrations were observed at 0.5 or 1 h post-dose for majority tissues (28 of 42). The highest concentrations of radioactivity were found in the small intestine contents at 0.5 h (112.137 µg equiv/g), urinary bladder contents at 3 h (89.636 µg equiv/g) and probably reflect excretion of drug and metabolites. The highest concentrations in specific organs were found in the renal cortex at 1 h (28.582 µg equiv/g), small intestine at 3 h (16.946 µg equiv/g), Harderian gland at 3 h (12.332 µg equiv/g) and pancreas at 3 h (12.635 µg equiv/g). Concentrations in the cerebrum (1.978 µg equiv/g), cerebellum (2.109 µg equiv/g), medulla (1.797 µg equiv/g) and spinal cord (1.510 µg equiv/g) were maximal at 0.5 h post-dose and persisted for 7 days. 4. The predicted total body and target organ exposures for humans given a single 100 µCi IV dose of [(14)C]VNP40101M were well within the medical guidelines for maximum radioactivity exposures in human subjects.

摘要
  1. 洛莫司汀(VNP40101M,也称为氯乙肼)是一种新型的磺酰肼类烷化剂(抗癌剂)。本文描述了使用定量全身放射自显影(QWBA)和质量平衡法来研究[(14)C]VNP40101M静脉注射给大鼠后的组织分布、排泄质量平衡和药代动力学。给大鼠静脉注射单次10mg/kg的[(14)C]VNP40101M推注剂量。

  2. 第1组动物在7天内放射性的回收率平均为给药剂量的92.1%,这在排泄物和尸体中得到体现。大部分放射性在48小时内通过尿液排出(48%),粪便中排出较少(5%),呼出气体中占11%。[(14)C]洛莫司汀的血浆半衰期约为62分钟,血浆峰浓度(Cmax)平均为8.3μg/mL。

  3. QWBA研究表明,在给雄性有色Long-Evans大鼠静脉注射单次10mg/kg的[(14)C]VNP40101M推注剂量后,给药后7天内药物衍生的放射性广泛分布于组织中。大多数组织(42个中的28个)在给药后0.5或1小时观察到最大浓度。给药后0.5小时小肠内容物中的放射性浓度最高(112.137μg当量/g),给药后3小时膀胱内容物中的放射性浓度最高(89.636μg当量/g),这可能反映了药物和代谢物的排泄。特定器官中最高浓度在给药后1小时出现在肾皮质(28.582μg当量/g),给药后3小时出现在小肠(16.946μg当量/g)、哈德氏腺(12.332μg当量/g)和胰腺(12.635μg当量/g)。大脑(1.978μg当量/g)、小脑(2.109μg当量/g)、延髓(1.797μg当量/g)和脊髓(1.510μg当量/g)中的浓度在给药后0.5小时达到最大值,并持续7天。

  4. 对于静脉注射单次100μCi[(14)C]VNP40101M的人类,预测的全身和靶器官暴露量完全在人类受试者最大放射性暴露的医学指南范围内。

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