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食物导致阿替洛尔生物利用度降低。

Food-induced reduction in bioavailability of atenolol.

作者信息

Melander A, Stenberg P, Liedholm H, Scherstén B, Wåhlin-Boll E

出版信息

Eur J Clin Pharmacol. 1979 Nov;16(5):327-30. doi: 10.1007/BF00605630.

Abstract

The influence of food intake on the bioavailability of the beta-adrenoceptor blocker atenolol was assessed by measurement of its single-dose kinetics in ten healthy volunteers, who took 100 mg both in the fasting state and together with a standardized breakfast. Food intake significantly shortened the time to reach peak concentration (2.7 h vs 1.5 h), but caused a significant reduction in AUC values, the mean decrease being 20%. The elimination half-life was unaffected. Atenolol, which is relatively hydrophilic, is incompletely absorbed in the fasting state, and escapes first-pass metabolism. The present findings indicate that food intake causes further impairment of its absorption, even though the absorption rate may initially be enhanced. This contrasts with previous observations on the more lipophilic beta-adrenoceptor blockers propranolol and metoprolol.

摘要

通过测定10名健康志愿者单剂量的动力学情况,评估了食物摄入对β-肾上腺素受体阻滞剂阿替洛尔生物利用度的影响。这些志愿者在禁食状态下和与一份标准化早餐一起服用了100毫克阿替洛尔。食物摄入显著缩短了达到峰值浓度的时间(分别为2.7小时和1.5小时),但导致AUC值显著降低,平均降幅为20%。消除半衰期未受影响。阿替洛尔相对亲水性较强,在禁食状态下吸收不完全,且逃过首过代谢。目前的研究结果表明,尽管食物摄入最初可能会提高阿替洛尔的吸收速率,但会进一步损害其吸收。这与之前对亲脂性更强的β-肾上腺素受体阻滞剂普萘洛尔和美托洛尔的观察结果形成对比。

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