Green A R, Aronson J K, Cowen P J
Br J Clin Pharmacol. 1985 Oct;20(4):317-21. doi: 10.1111/j.1365-2125.1985.tb05070.x.
The pharmacokinetics of L-tryptophan (5 g and 7.5 g) have been studied after its intravenous administration to healthy subjects and the results compared with those obtained after oral administration (0.7 g-3.5 g). In order to do this, we have re-analysed previously published data relating to oral administration. The data obtained following the oral administration of L-tryptophan suggest that the total body clearance and apparent volume of distribution are saturable. The pharmacokinetics of tryptophan after intravenous administration of 5 g and 7.5 g were similar to those after the oral administration of 25 and 50 mg kg-1 (i.e. 1.75 g and 3.5 g). Similar pharmacokinetic values were obtained following intravenous tryptophan when the same subjects were retested after a period of 2-4 weeks.
已对健康受试者静脉注射5克和7.5克L-色氨酸后的药代动力学进行了研究,并将结果与口服给药(0.7克至3.5克)后获得的结果进行了比较。为了做到这一点,我们重新分析了先前发表的与口服给药相关的数据。口服L-色氨酸后获得的数据表明,全身清除率和表观分布容积是可饱和的。静脉注射5克和7.5克色氨酸后的药代动力学与口服25和50毫克/千克(即1.75克和3.5克)后的药代动力学相似。在2至4周后对同一受试者进行重新测试时,静脉注射色氨酸后获得了相似的药代动力学值。