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Pharmacokinetic Studies of [~14C]Urea (1); Absorption, Distribution, Metabolism and Excretion after Single Administration of [~14C] Urea in Fasted Rats

机译:[〜14C]尿素的药代动力学研究(1);禁食大鼠单次服用[〜14C]尿素后的吸收,分布,代谢和排泄

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Absorption, distribution, metabolism and excretion after a single intravenous and oral administration of [~14C] urea at a dose of 2 mg/kg were investigated in fasted rats.1.Both radioactivity levels in plasma after intravenous and oral administration of [~14C] urea were decreased biphasically with t_(1/2#alpha#) of about 2.0 hr had t~(1/2#beta#) of about 3.5 hr. After oral administration, the plasma concentration reached C_max at 0.5 hr, suggesting rapid absorption of urea in the gastrointestinal tract.2.Radioactivity levels in most tissues reached C_max at 0.5 hr after oral administration, similar to that observed in the plasma. Excluding the radioactivity present in the digestive tract where [~14C] urea was administered, the concentrations in the kidney and urinary bladder were the highest in the examined tissues and were 3.2 and 2.5 times as high as that in plasma. The concentrations in other tissues were similar to , or lower than the plasma concentration. Subsequently, the concentrations in most tissues rapidly decreased in parallel with the plasma concentration.3.In plasma at 0.5 hr and 8hr after oral administration and in the urine collected for 24 hr after intravenous and oral administration, the major component of radioactivity was the unchanged drug and other metabolites were not observed. One may concluded that urea was almost not metabolized in fasted rats, considering the results of the excretion study, in which more than about 90% of dose radioactivity was excreted in urine as unchanged drug.4.Within 96 hr, 91.1%, 0.3% and 4.7% of dosed radioactivity were excreted in urine, feces and expired air after intravenous administration, and 95.1%, 1.2% and 3.5% after oral administration, respectively. The bioavailability estimated from the ratio of urinary excretion of urea after oral administration to that after intravenous administration was almost 100%.
机译:研究了禁食大鼠单次静脉和口服2 mg / kg [〜14C]尿素后的吸收,分布,代谢和排泄。1。静脉和口服[〜14C]血浆中两种放射性水平尿素双相减少,t_(1/2#alpha#)约为2.0小时,t〜(1/2#beta#)约为3.5小时。口服后0.5小时血浆浓度达到C_max,表明尿素在胃肠道迅速吸收。2.口服后0.5小时大多数组织的放射性水平达到C_max,与血浆中观察到的相似。排除存在[〜14C]尿素的消化道中存在的放射性,肾脏和膀胱中的浓度在被检查的组织中最高,分别是血浆中的3.2和2.5倍。其他组织中的浓度类似于或低于血浆浓度。随后,大多数组织中的浓度与血浆浓度同时迅速降低。3。口服后0.5小时和8小时的血浆中以及静脉内和口服后24小时收集的尿液中,放射性的主要成分保持不变没有观察到药物和其他代谢产物。可能会得出结论,考虑到排泄研究的结果,禁食大鼠尿素几乎没有被代谢,尿中约90%的剂量放射性作为未改变的药物排泄到尿中。4。在96小时内,91.1%,0.3%静脉给药后,尿中的粪便,粪便和呼出的空气中排泄的放射性剂量分别为4.7%和4.7%,口服后分别为95.1%,1.2%和3.5%。由口服给药后尿素排泄与静脉内给药后尿素排泄的比例估算的生物利用度几乎为100%。

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