Suppr超能文献

食物对以缓释片和微粒形式给药的茶碱吸收的影响。

Influence of food on the absorption of theophylline administered in the form of sustained release tablet and microgranules.

作者信息

Delhotal-Landes B, Flouvat B, Boutin M S, Karpouzas I, Prinseau J

机构信息

Department of Clinical Pharmacology, Ambroise Paré Hospital, Boulogne-Billancourt, France.

出版信息

Biopharm Drug Dispos. 1988 Jan-Feb;9(1):19-29. doi: 10.1002/bod.2510090104.

Abstract

Two sustained-release formulations of theophylline, tablets (T) and microgranules (MG) forms, were administered in a randomized order to 8 healthy subjects in fasting or with a high-protein test meal (50 per cent). Blood was collected for 32h post-dose. In fasting subjects, absorption of theophylline was significantly faster for T (tmax 5 h) as compared with MG (tmax 8 h, p less than 0.05), but Cmax and AUC were comparable; intersubject variability was higher with T. Administration of a high-protein test meal with T produced a significant decrease of the zero-order absorption rate constant of theophylline (K omicron 37.8 +/- 9.1 mgh-1 after meal versus 58.8 +/- 13 mgh-1 in fasting, p = 0.01), tmax was doubled to 10 h, and Cmax increased by 25 per cent (6.33 +/- 2.16 mgl-1 versus 5.04 +/- 1.28 mgl-1, p less than 0.02); with MG, tmax were the same (8 h), Cmax were not significantly increased (4.79 +/- 0.84 mgl-1 versus 4.55 +/- 0.67 mgl-1), absorption was delayed (lag-time 1.28 +/- 0.58 h) and the absorption was slightly accelerated (K omicron 50.4 +/- 10.4 mgh-1 versus 42.3 +/- 11.9 mgh-1, NS). For each form bioavailability was not significantly modified by food. This study demonstrated that food rich in protein modifies the absorption rate of theophylline in a sustained-release tablet formulation but is without influence in a pH-independent, sustained-release microgranule formulation.

摘要

两种茶碱缓释制剂,即片剂(T)和微粒剂(MG),以随机顺序给予8名健康受试者,受试者处于禁食状态或食用高蛋白试验餐(占比50%)。给药后32小时采集血样。在禁食受试者中,与MG(达峰时间8小时,p<0.05)相比,T制剂中茶碱的吸收明显更快(达峰时间5小时),但峰浓度和药时曲线下面积相当;T制剂的个体间变异性更高。T制剂与高蛋白试验餐一起服用时,茶碱的零级吸收速率常数显著降低(餐后为37.8±9.1mg/h,禁食时为58.8±13mg/h,p = 0.01),达峰时间加倍至10小时,峰浓度增加25%(分别为6.33±2.16mg/L和5.04±1.28mg/L,p<0.02);对于MG制剂,达峰时间相同(8小时),峰浓度没有显著增加(分别为4.79±0.84mg/L和4.55±0.67mg/L),吸收延迟(滞后时间1.28±0.58小时),吸收略有加速(零级吸收速率常数分别为50.4±10.4mg/h和42.3±11.9mg/h,无统计学差异)。对于每种制剂,食物对生物利用度没有显著影响。本研究表明,富含蛋白质的食物会改变茶碱缓释片剂制剂的吸收速率,但对pH值不依赖的缓释微粒剂制剂没有影响。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验