DEVELOPMENT AND VALIDATION OF STABILITY-INDICATING HPLC METHOD FOR DETERMINATION OF CEFPIROME SULFATE

被引:1
|
作者
Zalewski, Przemyslaw [1 ]
Skibinski, Robert [2 ]
Cielecka-Piontek, Judyta [1 ]
Bednarek-Rajewska, Katarzyna [3 ]
机构
[1] Poznan Univ Med Sci, Dept Pharmaceut Chem, PL-60780 Poznan, Poland
[2] Med Univ Lublin, Dept Med Chem, PL-20090 Lublin, Poland
[3] Poznan Univ Med Sci, Fac Med 1, Dept Clin Pathomorphol, PL-60355 Poznan, Poland
来源
ACTA POLONIAE PHARMACEUTICA | 2014年 / 71卷 / 05期
关键词
method validation; stability-indicating method; cefpirome sulfate; DEGRADATION KINETICS; STRESS DEGRADATION; CEFUROXIME AXETIL; CEFOSELIS SULFATE; TEMPERATURE; CEFEPIME; BUFFERS; TISSUE; PH;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The stability-indicating LC assay method was developed and validated for quantitative determination of cefpirome sulfate (CPS) in the presence of degradation products formed during the forced degradation studies. An isocratic HPLC method was developed with Lichrospher RP-18 column, 5 mu m particle size, 125 mm x 4 mm column and 12 mM ammonium acetate-acetonitrile (90: 10 v/v) as a mobile phase. The flow rate of the mobile phase was 1.0 mL/min. Detection wavelength was 270 nm and temperature was 30 degrees C. Cefpirome sulfate as other cephalosporins was subjected to stress conditions of degradation in aqueous solutions including hydrolysis, oxidation, photolysis and thermal degradation. The developed method was validated with regard to linearity, accuracy, precision, selectivity and robustness. The method was applied successfully for identification and determination of cefpirome sulfate in pharmaceuticals and during kinetic studies.
引用
收藏
页码:731 / 736
页数:6
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