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HPLC法测定生物样品中盐酸奈福泮的含量

Determination of Nefopam in Plasma by HPLC

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【作者】 谢林张晓楠严铭娟张琳刘晓东

【Author】 XIE Lin, ZHANG Xiao-Nan 1, YAN Ming-Juan, ZHANG Lin, LIU Xiao-Dong Center of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing 210009; \+1Center Lab of Fourth Medical University of PLA, Xian 710032

【机构】 中国药科大学药物代谢研究中心!南京210009第四军医大学中心实验室!西安710032

【摘要】 建立了血浆中盐酸奈福泮的HPLC测定法。血浆样品采取液 液两步提取后 ,以ODS HypersilC18为固定相 ,35 %乙腈∶6 5 % 0 .0 1mol/L庚烷磺酸钠 (pH =3 .0 )为流动相。紫外检测波长 2 15nm。最低检测浓度为 2 .5ng/ml,线性范围 2 .5~ 5 0 0 .0ng/ml(r =0 .9995 ) ,四种浓度的回收率大于 90 % ,日间日内变异系数小于15 %。

【Abstract】 An reversed phase HPLC method was established for determination of nefopam in plasma. The drug was extracted from plasma by liquid-liquid phase. ODS-Hypersil C 18 column was used. Mobile phase consisted of 35% acetonitrile∶65% 0.01 mol/L sodium heptane sulfonate(pH=3.0).The eluted peaks were detected by UV detector at 215 nm. The recoveries of nefopam from plasma were larger than 90% and RSD of intra-day and inter-day were smaller than 15% . Calibration curves were linear over 2.5~500.0 ng/ml(r=0.9995) and the minimum quantitative concentration was 2.5 ng/ml. The method was successfully used to study pharmcokinetics of nefopam in both dog and human.

【关键词】 盐酸奈福泮药代动力学HPLC含量测定
【Key words】 NefopamPharmacokineticsHPLCDeterminatino of content
  • 【文献出处】 中国药科大学学报 ,JOURNAL OF CHINA PHARMACEUTICAL UNIVERSITY , 编辑部邮箱 ,2000年05期
  • 【分类号】R927
  • 【被引频次】15
  • 【下载频次】122
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