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HPLC法测定头孢特仑新戊酯片的含量 被引量:3

HPLC determination of content of cefteram pivoxil tablets
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摘要 目的:建立头孢特仑新戊酯片含量测定的高效液相色谱方法。方法:采用岛津CLASS VP C18(250mm×4.6mm,5μm)色谱柱;以乙腈:醋酸钠缓冲液(35:65)为流动相;以对羟基苯甲酸甲酯为内标;检测波长254nm;调整流量使头孢特仑新戊酯峰的保留时间为14min。结果:头孢特仑新戊酯的线性范围为100~1000μg·mL^-1,r=0.9999,平均回收率为99.63%,RSD为0.57%。结论:本法可用于头孢特仑新戊酯片的含量测定,操作简便,结果准确。 Objective:To establish a HPLC method for the determination of cefteram pivoxil tablets. Method: Shimadzu CLASS VP C18 column (250 mm × 4.6 mm, 5μm) was selected, with a mobile phase consists of ace-tonitrile -0.05 mol·L^-1 sodium acetate buffer solution (35: 65 ), at a detection wavelength as 254 nm. The in-ternal standard was methyl p-hydroxybenzoate, and the flow rate was adjusted to make the retention time of cefteram pivoxil about 14 minute. Results: The calibration curve was proved to be linear in the range of 100~1000μg·mL^-1(r=0. 9999). The average recovery was 99.63% (RSD=0.57% ). Conclusion: The proposed method is simple, sensitive and accurate.
出处 《药学与临床研究》 2007年第3期210-212,共3页 Pharmaceutical and Clinical Research
关键词 HPLC 头孢特仑酯新戊酯片 含量 HPLC Cefteram pivoxil tablets Content
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参考文献3

  • 1袁莉娟,张玉凤.头孢特伦酯[J].中国新药杂志,1998,7(2):98-99. 被引量:7
  • 2日本抗生物质学术协议会.日本抗生物质医药品基准解说[S].东京:药业时报社,1998.90.
  • 3Sasaki H,Narita H.Cephalosporins,process for producing the same,intermediates thereof and process for producing the intermediates:JP,US5144027[P].1992-09-01.

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