Hussain F N, Ajjan R A, Moustafa M, Weir N W, Riley S A
Department of Gastroenterology, Northern General Hospital, Sheffield.
Br J Clin Pharmacol. 1998 Aug;46(2):173-5. doi: 10.1046/j.1365-2125.1998.00762.x.
Delayed-release formulations of mesalazine often rely on the gastrointestinal luminal pH profile to deliver 5-aminosalicylic acid (5ASA) to the colon. The aim of this study was to examine the influence of luminal pH on mesalazine release.
We studied the effect of co-administration of omeprazole and lactulose on the steady-state pharmacokinetics of Eudragit S-coated mesalazine in healthy volunteers.
No significant changes in urinary or faecal levels of 5ASA or its main metabolite, N-acetyl 5ASA, were apparent.
This study suggests that co-administration of omeprazole and lactulose does not impair the release of delayed-release mesalazine.
美沙拉嗪缓释制剂通常依赖胃肠道腔内的pH值分布将5-氨基水杨酸(5ASA)输送至结肠。本研究的目的是考察腔内pH值对美沙拉嗪释放的影响。
我们研究了在健康志愿者中联合使用奥美拉唑和乳果糖对Eudragit S包衣美沙拉嗪稳态药代动力学的影响。
5ASA及其主要代谢产物N-乙酰5ASA的尿液或粪便水平未见明显变化。
本研究表明,联合使用奥美拉唑和乳果糖不会损害美沙拉嗪缓释制剂的释放。