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Distribution and metabolism in healthy volunteers of disodium azodisalicylate a potential therapeutic agent for ulcerative colitis.

机译:在健康志愿者中偶氮二水杨酸二钠(一种溃疡性结肠炎的潜在治疗剂)的分布和代谢。

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摘要

A series of experiments has been performed in healthy male volunteers to investigate the disposition of orally administered disodium azodisalicylate, a potentially useful drug for the treatment of ulcerative colitis. The drug was given by mouth in doses of up to 2 g a day for six weeks and there were no adverse effects. Serum concentrations of the intact compound were low and the serum half-time was 4-12.8 days, probably because of a combination of a low clearance rate and a high apparent volume of distribution. Less than 5% of the ingested dose was excreted unchanged in the urine. Circulating concentrations of 5-ASA and N-acetyl-5-ASA were low and 30% of the equivalent daily dose was excreted in the urine, predominantly as N-acetyl-5-ASA. In most subjects more than 30% of the equivalent daily dose of 5-ASA was recovered from the faeces, either as 5-ASA itself or as the acetylated derivative. As 5-ASA has been shown to be the active therapeutic moiety of sulphasalazine, disodium azodisalicylate appears to be suitable for therapeutic trial in ulcerative colitis.
机译:已在健康的男性志愿者中进行了一系列实验,以研究口服给药的偶氮二水杨酸二钠的处置方式,这是一种可能用于治疗溃疡性结肠炎的药物。每天最多口服2 g的药物口服,持续6周,并且没有副作用。完整化合物的血清浓度低,血清半衰期为4-12.8天,这可能是由于清除率低和表观分布量大的原因所致。不到5%的摄入剂量不变地排泄到尿液中。 5-ASA和N-乙酰基-5-ASA的循环浓度很低,尿中排泄了当量每日等效剂量的30%,主要是N-乙酰基-5-ASA。在大多数受试者中,以5-ASA本身或乙酰化衍生物的形式从粪便中回收了超过30%的当量日剂量5-ASA。由于5-ASA已被证明是柳氮磺吡啶的活性治疗部分,因此偶氮二水杨酸二钠似乎适用于溃疡性结肠炎的治疗试验。

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