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高效液相色谱法测定盐酸班布特罗胶囊的含量 被引量:1

HPLC Determination of the content of Banbuterol hydrochloride capsule
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摘要 目的:建立测定胶囊剂中盐酸班布特罗含量的方法。方法:采用高效液相色谱法对胶囊剂中盐酸班布特罗含量进行测定。色谱条件:色谱柱Agilent Zorba×SB-C_(18),150mm×4.6mm;流动相:磷酸缓冲溶液-甲醇-乙腈(45:16:25),流速1mL·min^(-1);柱温25℃;检测波长220nm。结果:线性范围25.2~201.6μg·mL^(-1)(r=0.9999),回收率99.74%,RSD= 0.82%。结论:高效液相色谱法测定胶囊剂中盐酸班布特罗的含量方法简便易行,准确度高,重现性好,可用于控制该制剂的质量。 Objective:HPLC method to determined the content of Bambuterol hydrochloride has been established. Methods:The Agilent Zorbax SB -C18, 150 mm×4. 6 mm column was used with mobile phase phosphoric buffer solution -methanol- acetonitrile (45: 16:25 ) , the detection wavelenth was 220 nm. Result: The Linear concentration was within the range of 25.2 - 201.6μg·mL^- 1 ( r = 0. 9999 ), and the average recovery was 99. 74% ( RSD = 0. 82%. Conclusion:The HPLC method to determined content of Banbuterol hydrochloride in capsule was simple and reliable. The method can be used to control the quality of preparation.
出处 《药物分析杂志》 CAS CSCD 北大核心 2006年第9期1323-1324,共2页 Chinese Journal of Pharmaceutical Analysis
关键词 高效液相色谱法 盐酸班布特罗 胶囊剂 HPLC Banbuterol hydrochloride capsule
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  • 1苏国强,侯建英,朱崇泉,边军,冷宗康.班布特罗的合成[J].中国药科大学学报,1999,30(4):251-252. 被引量:6
  • 2ZHANGLiang(张亮) GUMing(顾明) WANGYing(王颖)etal.Quantitative determination of terbutalin in human plasma after administration of bambuterol using liquid chromatography — electrospray ionization mass spectrometry[J].中国药科大学学报,2001,32(5):365-365.
  • 3Lindbeg C, Jonsson S, Paulson J. Determination of banbuterol, a prodrug of terbutaline, in plasma and urine by gas chromatography/mass spectrometry · Biomed Environ Mass Spectrom,1990,19 :218

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