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首页> 外文期刊>Alimentary pharmacology & therapeutics. >Review article: 5-aminosalicylate formulations for the treatment of ulcerative colitis - methods of comparing release rates and delivery of 5-aminosalicylate to the colonic mucosa.
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Review article: 5-aminosalicylate formulations for the treatment of ulcerative colitis - methods of comparing release rates and delivery of 5-aminosalicylate to the colonic mucosa.

机译:综述文章:5-氨基水杨酸制剂用于治疗溃疡性结肠炎-比较5-氨基水杨酸向结肠粘膜的释放速率和释放的方法。

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摘要

Summary Background Many oral 5-aminosalicylic acid (5-ASA) formulations are designed to maximize 5-ASA release in the colon where it acts topically on the colonic mucosa. Delayed-release formulations and azo-prodrugs minimize 5-ASA absorption in the upper gastrointestinal (GI) tract. Aims To review methods for assessing 5-ASA release and colonic distribution from oral formulations, and the potential use of this information for guiding clinical decisions. Methods PubMed and recent conference abstracts were searched for articles describing techniques used to assess 5-ASA release from ulcerative colitis (UC) therapies. Results In-vitro GI models, although unable to simulate more complex aspects of GI physiology, can provide useful data on 5-ASA release kinetics and bioaccessibility. Gamma-scintigraphy is useful for investigating GI disintegration of different formulations, but may not accurately reflect 5-ASA distribution. Plasma pharmacokinetic studies provide data on systemic exposure, but not on colonic distribution or mucosal uptake. Mucosal biopsies provide direct evidence of colonic distribution and may predict clinical efficacy, but must be interpreted cautiously because of considerable inter-subject variability and other confounding factors. Conclusion While assessment of 5-ASA release is important, limitations of individual measurement techniques mean that randomized clinical studies in UC patients remain the best guide for dosing and treatment regimen decisions.
机译:背景技术许多口服的5-氨基水杨酸(5-ASA)制剂被设计成最大化5-ASA在结肠中的释放,在结肠中它局部作用于结肠粘膜。延迟释放的制剂和偶氮前药使上消化道(GI)的5-ASA吸收最小化。目的回顾评估口服制剂中5-ASA释放和结肠分布的方法,以及该信息在指导临床决策中的潜在用途。方法在PubMed和最近的会议摘要中搜索有关描述用于评估溃疡性结肠炎(UC)治疗中5-ASA释放的技术的文章。结果体外GI模型虽然不能模拟GI生理学的更复杂方面,但可以提供有关5-ASA释放动力学和生物可及性的有用数据。伽玛闪烁描记法可用于研究不同配方的胃肠道崩解,但可能无法准确反映5-ASA分布。血浆药代动力学研究提供了全身暴露的数据,但没有结肠分布或粘膜摄取的数据。粘膜活组织检查可提供结肠分布的直接证据,并可预测临床疗效,但由于受试者之间的差异较大以及其他混杂因素,必须谨慎解释。结论虽然评估5-ASA的释放很重要,但个别测量技术的局限性意味着UC患者的随机临床研究仍是剂量和治疗方案决策的最佳指南。

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