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柳氮磺胺吡啶的临床药代动力学

Clinical pharmacokinetics of sulphasalazine.

作者信息

Das K M, Dubin R

出版信息

Clin Pharmacokinet. 1976 Nov-Dec;1(6):406-25. doi: 10.2165/00003088-197601060-00002.

Abstract

Sulphasalazine consists of 5-aminosalicylic acid and sulphapyridine both linked together by an azo bond. Sulphasalazine is clearly useful in long-term management of ulcerative colitis and may be useful in Crohn's disease. The absorption, metabolism and excretion of sulphasalazine is similar in volunteers and patients with ulcerative colitis or Crohn's disease. Sulphasalazine serves as a vehicle to deliver its possible active components, 5-aminosalicylic acid and sulphapyridine, to the colon in higher concentrations than could be achieved by oral administration of either one alone. Sulphasalazine reaches the colon mostly unchanged and is split by gut bacteria at the azo linkage, releasing 5-aminosalicylic acid and sulphapyridine. 5-Aminosalicylic acid may act locally and is not absorbed to any great extent. On the contrary, sulphapyridine is mostly absorpbed from the colon and may act both locally, during mucosal absorption, and systemically. A positive correlation exists between serum total sulphapyridine concentration and both therapeutic efficacy and toxicity. Sulphapyridine metabolism is largely determined by inherited acetylator phenotype, either slow or fast. Slow acetylators have higher levels of free sulphapyridine and lower levels of acetylated sulphapyridine than fast acetylators, and are likely to have more toxic symptoms on equivalent doses of sulphasalazine. Therapeutic effects of sulphasalazine in ulcerative colitis and Crohn's disease correlate with serum concentrations of total sulphapyridine (20 to 50 microng/ml), and toxicity with total sulphapyridine concentration greater than 50 microng/ml. Side-effects are mostly observed among slow acetylators. In long-term therapy of ulcerative colitis doses of 2 to 3g/day of sulphasalazine are most likely to sustain remissions and avoid toxicity. During therapy with sulphasalazine, determination of acetylator phenotype and total sulphapyridine concentration can guide effective dosage and avoid side-effects. A single serum sample for free and acetylated sulphapyridine concentrations is sufficient for this purpose.

摘要

柳氮磺胺吡啶由5-氨基水杨酸和磺胺吡啶通过偶氮键连接而成。柳氮磺胺吡啶在溃疡性结肠炎的长期管理中显然有用,对克罗恩病可能也有用。柳氮磺胺吡啶在志愿者以及溃疡性结肠炎或克罗恩病患者中的吸收、代谢和排泄情况相似。柳氮磺胺吡啶作为一种载体,能够将其可能的活性成分5-氨基水杨酸和磺胺吡啶以比单独口服其中任何一种更高的浓度输送至结肠。柳氮磺胺吡啶大多未发生变化地抵达结肠,并在偶氮键处被肠道细菌分解,释放出5-氨基水杨酸和磺胺吡啶。5-氨基水杨酸可能在局部起作用,且不会被大量吸收。相反,磺胺吡啶大多从结肠吸收,可能在黏膜吸收过程中在局部起作用,也可能产生全身作用。血清总磺胺吡啶浓度与治疗效果和毒性之间存在正相关。磺胺吡啶的代谢很大程度上由遗传的乙酰化表型决定,即慢乙酰化型或快乙酰化型。与快乙酰化者相比,慢乙酰化者的游离磺胺吡啶水平更高,乙酰化磺胺吡啶水平更低,在等量柳氮磺胺吡啶剂量下更可能出现毒性症状。柳氮磺胺吡啶在溃疡性结肠炎和克罗恩病中的治疗效果与总磺胺吡啶血清浓度(20至50微克/毫升)相关,毒性则与总磺胺吡啶浓度大于50微克/毫升相关。副作用大多在慢乙酰化者中观察到。在溃疡性结肠炎的长期治疗中,每天2至3克柳氮磺胺吡啶的剂量最有可能维持缓解并避免毒性。在柳氮磺胺吡啶治疗期间,测定乙酰化表型和总磺胺吡啶浓度可指导有效剂量并避免副作用。为此目的,一份用于检测游离和乙酰化磺胺吡啶浓度的血清样本就足够了。

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