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食物对健康老年男性中维拉克林(HP 029)生物利用度的影响:一种潜在的抗阿尔茨海默病药物。

The effect of food on the bioavailability of velnacrine (HP 029) in healthy elderly men: a potential Alzheimer agent.

作者信息

Puri S K, Hsu R S, Ho I, Lassman H B

机构信息

Section of Clinical Pharmacology, Hoechst-Roussel Pharmaceuticals Inc., Somerville, NJ 08876.

出版信息

J Clin Pharmacol. 1989 Oct;29(10):956-60. doi: 10.1002/j.1552-4604.1989.tb03261.x.

Abstract

Velnacrine (HP 029; 1,2,3,4-tetrahydro-9-aminoacridin-1-ol-maleate) is an investigational drug being studied in patients with Alzheimer's disease. In this open, randomized, crossover study, 24 healthy, elderly men were given 100 mg of velnacrine on two different study days to assess the influence of food on the bioavailability of velnacrine. On the first day, subjects received drug either after an overnight fast or 15 minutes after completing a standard breakfast. Seven days later, the treatments were crossed over. Blood and urine samples were collected at specific times and various intervals, respectively, from all subjects before and after drug administration for up to 24 hours. Plasma and urine concentrations of velnacrine were determined by an HPLC method. Administration of velnacrine with food resulted in slightly lower peak plasma levels of unconjugated velnacrine, (175 vs 213 ng/ml) and delayed times-to-peak plasma levels, (2.5 vs 1.5 h) without affecting the AUCs and the t 1/2 of the drug. The amount of unconjugated velnacrine excreted in urine was slightly higher when the drug was taken with food (19 vs 17 mg), but renal clearance was not altered. These results indicate that food delayed the rate but not the extent of velnacrine absorption. The minor differences in Cmax and tmax may not be clinically meaningful. Therefore, velnacrine can be administered with or without food.

摘要

韦那克林(HP 029;1,2,3,4-四氢-9-氨基吖啶-1-醇马来酸盐)是一种正在阿尔茨海默病患者中进行研究的试验性药物。在这项开放性、随机、交叉研究中,24名健康老年男性在两个不同的研究日服用100毫克韦那克林,以评估食物对韦那克林生物利用度的影响。第一天,受试者在禁食过夜后或完成标准早餐15分钟后服用药物。七天后,治疗方案交叉。在给药前和给药后长达24小时的特定时间和不同间隔,分别从所有受试者采集血液和尿液样本。采用高效液相色谱法测定韦那克林的血浆和尿液浓度。与食物一起服用韦那克林导致未结合韦那克林的血浆峰值水平略低(175对213纳克/毫升),血浆达峰时间延迟(2.5对1.5小时),但不影响药物的AUC和t1/2。与食物一起服用药物时,尿液中排泄的未结合韦那克林量略高(19对17毫克),但肾脏清除率未改变。这些结果表明,食物延迟了韦那克林的吸收速率,但没有影响吸收程度。Cmax和tmax的微小差异可能没有临床意义。因此,韦那克林可以与食物一起服用,也可以不与食物一起服用。

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