高效液相色谱法测定盐酸氟西汀的含量
投稿时间:2013-05-22  修订日期:2014-04-07  点此下载全文
引用本文:吴荷琴,陈朝霞.高效液相色谱法测定盐酸氟西汀的含量[J].药学实践杂志,2015,33(1):58~59,82
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作者单位
吴荷琴 常州四药制药有限公司, 江苏 常州 213004 
陈朝霞 常州四药制药有限公司, 江苏 常州 213004 
中文摘要:目的 建立测定盐酸氟西汀含量的高效液相色谱法。方法 选用Agilent Eclipse XDB-C8柱(4.6 mm×250 mm,5 μm);流动相:四氢呋喃-甲醇-三乙胺缓冲液(取三乙胺10 ml,置1 000 ml量筒中,加水980 ml,用磷酸调节pH值至6.0)(30:10:60);流速为1.0 ml/min;检测波长:227 nm;进样量:10 μl;柱温:25℃。结果 方法的线性范围为55.17~165.51 μg/ml(r=0.999 9);最低检测限:0.15 μg/ml;回收率在99.9%~100.0%之间,重复性RSD为0.1%(n=6)。结论 方法简便灵敏, 结果准确可靠,可用于盐酸氟西汀的质量控制。
中文关键词:盐酸氟西汀  含量测定  高效液相色谱法
 
Determination of fluoxetine hydrochloride by HPLC
Abstract:Objective To establish an HPLC method for assay determination of fluoxetine hydrochloride. Methods Agilent Eclipse XDB-C8 (4.6 mm × 250 mm,5 μm) was used,mobile phase was tetrahydrofuran-methanol-triethylamine buffer (to 10 ml of triethylamine in a 1 000 ml flask,added 980 ml of water,pH was adjust to 6.0 by phosphoric acid) (30:10:60),flow rate was 1.0 ml/min,detection wavelength was 227 nm,injection volume was 10 μl,column temperature was 25℃. Results Linearity range was 55.17-165.51 μg/ml (r=0.999 9),minimum detection limit was 0.15 μg/ml,accuracy was between 99.9%-100.0%,repeatability RSD was 0.1% (n=6). Conclusion The method was accurate and reliable,which could be applied for quality control of fluoxetine hydrochloride.
keywords:fluoxetine hydrochloride  assay  HPLC
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