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高脂饮食对两种非诺贝特微粒化胶囊口服吸收的影响
引用本文:李中东,高志伟,施孝金,焦正,王蓓,钟明康,王宏图.高脂饮食对两种非诺贝特微粒化胶囊口服吸收的影响[J].中国药学杂志,2007,42(17):1337-1339.
作者姓名:李中东  高志伟  施孝金  焦正  王蓓  钟明康  王宏图
作者单位:复旦大学附属华山医院药剂科,上海,200040
摘    要: 目的比较在空腹和高脂饮食下非诺贝特微粒化胶囊的生物等效性,了解食物对非诺贝特微粒化胶囊吸收的影响。方法分别在空腹或高脂饮食下,24名成年健康志愿者单剂量口服两种非诺贝特微粒化胶囊,用HPLC测定血药浓度,对其药动学参数进行统计分析。结果在空腹时,非诺贝特微粒化胶囊和力平之胶囊的主要药动学参数分别为AUC0→96:(208.4±65.0),(155.7±108.9)mg·h·L-1,ρmax:(10.1±3.0),(5.3±3.8)mg·L-1;tmax:(4.1±0.6),(6.0±2.6)h。在高脂饮食时,非诺贝特微粒化胶囊和力平之胶囊的主要药动学参数分别为AUC0→96:(221.7±57.6),(220.5±58.2)mg·h·L-1,ρmax:(14.2±2.5),(14.4±2.6)mg·L-1;tmax:(4.9±0.9),(4.5±1.1)h。经统计学分析,在空腹条件下非诺贝特微粒化胶囊与力平之胶囊生物不等效,前者的相对生物利用度以AUC0→96计为(153.2±40.0)%。而在高脂饮食下,非诺贝特微粒化胶囊与力平之胶囊生物等效,前者的相对生物利用度为(101.2±12.0)%。结论非诺贝特微粒化胶囊的生物利用度受高脂饮食影响不明显,但饮食可提高其ρmax,而高脂饮食可显著提高力平之胶囊的AUC和ρmax

关 键 词:非诺贝特  非诺贝特酸  生物利用度  药动学  高效液相色谱法  微粒化  胶囊  饮食
文章编号:1001-2494f2007)17-1337-04
收稿时间:2006-04-29;
修稿时间:2006-04-29

Effect of Food on Relative Bioavailability of Fenofibrate Micronised Capsule
LI Zhong-dong,GAO Zhi-wei,SHI Xiao-jin,JIAO Zheng,WANG Bei,ZHONG Ming-kang,WANG Hong-tu.Effect of Food on Relative Bioavailability of Fenofibrate Micronised Capsule[J].Chinese Pharmaceutical Journal,2007,42(17):1337-1339.
Authors:LI Zhong-dong  GAO Zhi-wei  SHI Xiao-jin  JIAO Zheng  WANG Bei  ZHONG Ming-kang  WANG Hong-tu
Affiliation:Depart- ment of Pharmacy, Huashan Hospital, Fudan University, Shanghai 200040, China
Abstract:OBJECTIVE To investigate the effect of food on the relative bioavailability and pharmacokinetics of fenofibrate micronised capsule versus Lipanthyl capsule in healthy volunteers.METHODS Under fasting and high-fat breakfast fed condition,a single dose of 200 mg fenofibrate micronised capsule and Lipanthyl capsule was given to 24 healthy volunteers using an open-label,randomized,two-way crossover design.Fenofibric acid levels in plasma were determined by validated HPLC methods.RESULTS The pharmacokinetic parameters of fenofibrate micronised capsule and Lipanthyl capsule under fasting condition were as following:AUC0→96(208.4±65.0)and(155.7±108.9)mg·h·L-1,ρmax(10.1±3.0)and(5.33± 3.8)mg·L-1 tmax(4.1± 0.6)and(6.0±2.6)h,respectively.Then the main pharmacokinetic parameters of fenofibrate micronised capsule and Lipanthyl capsule under high-fat breakfast fed condition were as follows AUC0→96(221.7±57.6)and(220.5±58.2)mg·h·L-1,ρmax(14.2±2.5)and(14.4±2.6)mg·L-1,tmax(4.9±0.9)and(4.5±1.1)h,respectively.The relative bioavailability of fenofibrate micronised capsule versus Lipanthyl capsule under fast condition was(153.2±40.0)% and was bioinequivelent.Then under high-fat breakfast fed condition,the relative bioavailability of fenofibrate micronised capsule versus Lipanthyl capsule was(101.2±12.0)% and was bioequivalent.CONCLUSION High-fat breakfast can little modify either the relative bioavailability or pharmacokinetic profile(except ρmax)of fenofibrate micronised capsule,but the AUC and ρmax of Lipanthyl capsule can be highly increased under high-fat breakfast fed condition.
Keywords:fenofibrate  fenofibric acid  bioavailability  pharmacokinetics  HPLC  micronised  capsule  food
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