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美沙拉嗪从pH依赖性制剂中的释放:奥美拉唑和乳果糖联合给药的影响。

Mesalazine release from a pH dependent formulation: effects of omeprazole and lactulose co-administration.

作者信息

Hussain F N, Ajjan R A, Moustafa M, Weir N W, Riley S A

机构信息

Department of Gastroenterology, Northern General Hospital, Sheffield.

出版信息

Br J Clin Pharmacol. 1998 Aug;46(2):173-5. doi: 10.1046/j.1365-2125.1998.00762.x.

Abstract

AIMS

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.

METHODS

We studied the effect of co-administration of omeprazole and lactulose on the steady-state pharmacokinetics of Eudragit S-coated mesalazine in healthy volunteers.

RESULTS

No significant changes in urinary or faecal levels of 5ASA or its main metabolite, N-acetyl 5ASA, were apparent.

CONCLUSIONS

This study suggests that co-administration of omeprazole and lactulose does not impair the release of delayed-release mesalazine.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

相似文献

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Clinical pharmacokinetics of slow release mesalazine.缓释美沙拉嗪的临床药代动力学
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本文引用的文献

1
An oral preparation to release drugs in the human colon.一种在人体结肠释放药物的口服制剂。
Br J Clin Pharmacol. 1982 Sep;14(3):405-8. doi: 10.1111/j.1365-2125.1982.tb01999.x.
10
Effect of omeprazole on intragastric and duodenal bulb acidity in duodenal ulcer patients.
Aliment Pharmacol Ther. 1989 Apr;3(2):151-8. doi: 10.1111/j.1365-2036.1989.tb00201.x.

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