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Metabolism and urinary excretion of 5-amino salicylic acid in healthy volunteers when given intravenously or released for absorption at different sites in the gastrointestinal tract.

机译:静脉注射或在胃肠道的不同部位释放以吸收后健康志愿者体内的5-氨基水杨酸代谢和尿排泄。

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摘要

In six healthy subjects serum concentrations of 5 amino salicylic acid (5ASA) and acetyl 5ASA were measured for up to 24 hours, and urinary excretion over 48 hours. After an intravenous injection of 3.26 mmol 5ASA serum concentrations fell rapidly with a distribution half-life of 17 +/- 2 min and an elimination half-life of 42 +/- 5 min. After 45 minutes acetyl 5ASA became the dominant compound and after seven hours serum concentrations of both components were almost unrecordable. Orally ingested 5ASA in three preparations to ensure its release in the stomach, small intestine and ileocaecal region respectively gave lower serum concentrations and urinary excretion than those obtained after an intravenous infusion. Bioavailabilities which ranged from 19% for ileocaecal release to 75% for release in the upper gastrointestinal tract, were calculated from areas under the serum concentration curves. Urinary excretion of 5ASA and its acetyl metabolite over 48 hours was 78%, 52%, 55%, and 21% respectively of the dose given intravenously and orally for gastric, small intestinal and ileocaecal release.
机译:在六名健康受试者中,测定长达24小时的血清5氨基水杨酸(5ASA)和乙酰5ASA的血清浓度,并测定48小时的尿排泄量。静脉注射3.26 mmol后5ASA的血清浓度迅速下降,分布半衰期为17 +/- 2分钟,消除半衰期为42 +/- 5分钟。 45分钟后,乙酰基5ASA成为主要化合物,七小时后,两种成分的血清浓度几乎不可记录。口服摄入5ASA的三种制剂可确保其在胃,小肠和回盲区的释放,分别比静脉输注后的血清浓度和尿排泄量低。从血清浓度曲线下的面积计算生物利用度,从回肠释放的19%到上消化道的释放的75%。 5ASA及其乙酰代谢产物在48小时内的尿排泄量分别为静脉,口服给予胃,小肠和回盲肠的剂量的78%,52%,55%和21%。

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