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甲壳胺对硝苯地平片剂药代动力学和生物利用度的影响 被引量:1

The effects of chitin on the pharmacokinetics and the bioavailability of nifedipine tablet
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摘要 目的:测定甲壳胺对硝苯地平片剂药代动力学和生物利用度的影响。方法:采用气相色谱法研究了10 名男性健康志愿者随机单剂量口服市售片和以甲壳胺为辅料的硝苯地平片剂后,药物在体内的经时过程并计算药代动力学参数。结果:以甲壳胺为辅料的片剂和市售片的t1/2ka分别为0-41 h 和0-77 h,t1/2ke分别为2-64 h 和2-63 h ,tmax 分别为1-59 h 和2-03 h ,cmax分别为104-61 μg·L- 1 和57-36 μg·L- 1 ,AUC分别为586-18 μg·h·L-1 和342-27 μg·h·L-1 ,其相对生物利用度为151-8 % 。结论:甲壳胺可显著提高硝苯地平的生物利用度,明显改善药物的吸收。 OBJECTIVE: To determine the effects of chitin on the pharmacokinetics and the bioavailability of nifedipine tablet METHOD: By a random cross over arrangement, ten healthy volunteers received a single dose of either nifedipine tablet with chitin in it or nifedipine tablet bought from a drug store after an overnight fast The nifedipine in human plasma was detected by gas chromatography and the pharmacokinetic parameters were calculated RESULTS: t 1/2ka were 0 41 h and 0 77 h, respectively t 1/2ke were 2 64 h and 2 63 h, respectively The peak plasma levels with t max were 104 61 μg·L -1 at 1 59 h and 57 36 μg·L -1 at 2 03 h,respectively The area under the plasma concentration time curves were 586 18 μg·h·L -1 and 342 27 μg·h·L -1 , respectively The relative bioavailability was 151 8% CONCLUSION: The results showed that chitin could significantly raise the nifedipine bioavailability and improve the absorption of nifedipine in gastrointestinal tract
出处 《中国药学杂志》 CAS CSCD 北大核心 1999年第12期827-829,共3页 Chinese Pharmaceutical Journal
关键词 甲壳胺 硝苯地平 生物利用度 药代致力学 chitin, nifedipine, gas chromatography, bioavailability, pharmacokinetics
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  • 1黄园,药物分析杂志,1991年,11卷,312页
  • 2王申,中国药科大学学报,1991年,22卷,1页
  • 3杜青,中国医院药学杂志,1991年,6卷,265页
  • 4贡小清,中华医学检验杂志,1988年,6卷,335页
  • 5安登魁,药物分析,1992年,327页

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