Renwick A G, Ball L M, Corina D L, Williams R T
Xenobiotica. 1978 Aug;8(8):461-74. doi: 10.3109/00498257809056148.
Oral doses (20 mg/kg) of [Me-14C]toluene-2-sulphonamide were rapidly eliminated by rats (92% of dose in 24 h). Most of the 14C (88%) was recovered in the urine within 7 days with litte (5%) in the faeces. Larger oral doses (125 and 200 mg/kg) were eliminated more slowly (70 and 43% respectively in 24 h) but the overall distribution of 14C between urine and faeces was unchanged. 2. Low oral doses (0.2--0.4 mg/kg) of [Me-14C]toluene-2-sulphonamide were excreted more slowly in man than in the rat, with about 50% recovered in the urine in 24 h and 80% in 48 h. Negligible 14C (less than 1%) appeared in the faeces. 3. The main metabolites of toluene-2-sulphonamide were 2-sulphamoylbenzyl alcohol and its sulphate and glucuronic acid conjugates (80% of the 14C in the urine of rats and 35% in man) and saccharin (35% in man and 3% in the rat). Other metabolities found in the urine were 2-sulphamoylbenzoic acid (2% in the rat and 4% in man) and N-acetyltoluene-2-sulphonamide (6% in rat and 2% in man) together with unchanged compound (5% in rat and 3% in man).
大鼠经口给予剂量为20毫克/千克的[甲基-14C]甲苯-2-磺酰胺后,能迅速将其排出(24小时内排出剂量的92%)。7天内,大部分的14C(88%)通过尿液排出,少量(5%)通过粪便排出。较大的经口剂量(125和200毫克/千克)排出速度较慢(24小时内分别为70%和43%),但14C在尿液和粪便中的总体分布没有变化。2. 人体经口给予低剂量(0.2 - 0.4毫克/千克)的[甲基-14C]甲苯-2-磺酰胺后,排出速度比大鼠慢,24小时内约50%通过尿液排出,48小时内80%排出。粪便中出现的14C可忽略不计(不到1%)。3. 甲苯-2-磺酰胺的主要代谢产物为2-氨磺酰苄醇及其硫酸盐和葡萄糖醛酸结合物(大鼠尿液中14C的80%,人体中35%)和糖精(人体中35%,大鼠中3%)。尿液中发现的其他代谢产物有2-氨磺酰苯甲酸(大鼠中2%,人体中4%)和N-乙酰甲苯-2-磺酰胺(大鼠中6%,人体中2%)以及未变化的化合物(大鼠中5%,人体中3%)。