el-Dareer S M, White V, Chen F P, Mellett L B, Hill D L
Cancer Treat Rep. 1976 Nov;60(11):1627-31.
2-14C-tetrahydrouridine was prepared and used to determine the serum levels and excretion of tetrahydrouridine by varous experimental animals. In mice injected ip with the agent (50 mg/kg), the serum level of tetrahydrouridine was maximum (76 mug/ml) at 15 minutes. For rats injected with the same dose, the tetrahydrouridine content of serum was greatest (58 mug/ml) at 30 minutes. Within 3 hours, the serum content of the drug in both mice and rats fell to less than 10% of the maximum. The kidneys of mice selectively accumulated tetrahydrouridine; the concentration rose to 275 mug/g at 1 hour after injection. Nearly all of the dose was excreted unchanged in the urine of mice and rats in 24 hours. For a dog and a monkey given an iv dose (50 mg/kg) of tetrahydrouridine, serum levels of the agent were 210 and 200 mug/ml, respectively, at 5 minutes. The apparent half-lives for the initial phase of disappearance were 18 and 20 minutes and those for the later phase were 65 and 70 minutes, respectively. In 24 hours the dog and monkey excreted most of the dose as unchanged tetrahydrouridine. No metabolites were detected in the biologic samples from either species.
制备了2-¹⁴C-四氢尿苷,并用于测定各种实验动物体内四氢尿苷的血清水平和排泄情况。给小鼠腹腔注射该药物(50mg/kg)后,15分钟时四氢尿苷的血清水平最高(76μg/ml)。给大鼠注射相同剂量后,30分钟时血清中四氢尿苷含量最高(58μg/ml)。在3小时内,小鼠和大鼠血清中的药物含量均降至最高值的10%以下。小鼠的肾脏选择性地积累四氢尿苷;注射后1小时浓度升至275μg/g。几乎所有剂量在24小时内均以原形经小鼠和大鼠尿液排出。给狗和猴子静脉注射四氢尿苷(50mg/kg)后,5分钟时药物的血清水平分别为210和200μg/ml。消失初始阶段的表观半衰期分别为18和20分钟,后期阶段分别为65和70分钟。在24小时内,狗和猴子排出的大部分剂量为未代谢的四氢尿苷。在这两个物种的生物样品中均未检测到代谢产物。