期刊文献+

高效液相色谱法测定人血浆中的烟酸 被引量:3

Determination of nicotinic acid in human plasma by high performance liquid chromatography
下载PDF
导出
摘要 目的 建立人血浆中烟酸的高效液相色谱 (highperformanceliquidchromatography ,HPLC)测定方法。方法 以替硝唑为内标物 ,用乙腈直接沉淀人血浆中蛋白质 ,上清液在sphersorb色谱柱上 ,以乙腈 水 10 %四丁基氢氧化铵 (5 5∶4 5∶1)为流动相进行分离 ,流速 1ml·mim-1;柱温 30°C ;检测波长为 2 5 4nm。结果 烟酸与内标分离完全且无其他干扰 ,保留时间分别为 5 5 4、4 15min。线性范围 0 18~ 11 0 μg·ml-1,r=0 9999.日内RSD为 1 70~ 3 33% ,日间RSD为 1 75 %~ 4 11% ,回收率为 94 2 %~10 6 6 % ,血浆中烟酸的最低检测浓度为 0 0 9μg·ml-1。结论 所用方法简便、准确、重复性好 ,可用于口服烟酸缓释片后的血药浓度检测。 Objective TO establish a HPLC determination method for nicotinic acid in human plasma.Methods Using acetonitrile to deposit protein directly.The nicotinic acid and internal standard(Tinidazole) were separated on C 18 column with a mobile phase consisting of acetonitrile-water-10% tetrabutylammonium(55∶45∶1),with flow rate of 1ml·mim -1 ,and the detection wavelength was 254nm.Results Nicotinic acid was completely separated from the internal standard,and the retention time was 5.54min and 4.15min,respectively.The calibration curve was linear within 0.18~11.0μg·ml -1 ,r=0.999 9.The recoveries of methodology were 94.2%~106.6%.RSD within-day and between days were 1.70%~3.33% and 1.75%~4.11%,respectively.And the detection limit of nicotinic acid in human plasma was 0.09μg·ml -1 above.Conclusions The method is simple,accurate and repeatable.It has been successful in the determination of nicotinic acid in human plasma for pharmacokinetic studies.
出处 《广西医学》 CAS 2004年第9期1283-1285,共3页 Guangxi Medical Journal
关键词 烟酸 高效液相色谱 血药浓度 药物动力学 Nicotinic acid HPLC Drug concentration in plasma Pharmacokinetics
  • 相关文献

参考文献3

  • 1Hemgen N, Serberthn V, Hengen M. High-performance liquid chromatographic determination of free nicotinic and its metabolite acid in plasma and urine [J]. Clin Chem, 1978,24(10):1 740 - 1 743.
  • 2Ding RW, Kolbe K, Merz B, et al. Pharmacokinetics of nicotinic acid-salicylic acid interaction [ J]. Clin Pharmacol Ther, 1989,46(6) :642-647.
  • 3陈修.心血管药理学[M].北京:人民卫生出版社,1997.514.

共引文献35

同被引文献10

引证文献3

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部