摘要
目的:建立气相色谱法测定替普瑞酮含量的方法。方法:采用DB-FFAP弹性石英毛细管柱(30m×0.32mm×0.25μm);FID检测器;色谱条件:柱温为200℃;进样口温度为250℃;检测器温度为250℃;分流进样,分流比为1∶10。结果:替普瑞酮在0.1~10.0mg·mL-1范围内线性关系良好(r=0.9999,n=7);替普瑞酮的回收率(n=9)为98.0%~102.0%。结论:本测定方法准确、灵敏、专属性高,可作为替普瑞酮胶囊的含量测定方法。
Objective:To establish a GC method to determine the content of the terprenone capsules. Method:Using DB - FFAP capillary column(30 m × 0. 32 mm × 0.25 μm)and FID under the following chromatography condition:column temperature was set at 200℃, injector and detector temperature were both set at 250℃, split ratio was 1: 10. Result: The calibration curves showed a good linearity over the range of 0. 1 - 10. 0 mg· mL^-1(r = 0. 9999, n = 7 ). The recovery ( n = 9 ) of terprenone was 102. 0%. Conclusion: The method is specific, accurate, sensitive and suitable for the determination of terprenone capsules.
出处
《药物分析杂志》
CAS
CSCD
北大核心
2009年第6期998-1000,共3页
Chinese Journal of Pharmaceutical Analysis