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HPLC法测定头孢氨苄胶囊杂质F的研究
引用本文:唐秋菊,夏晟. HPLC法测定头孢氨苄胶囊杂质F的研究[J]. 中国药品标准, 2020, 21(2): 124-129
作者姓名:唐秋菊  夏晟
作者单位:重庆科瑞制药(集团)有限公司
摘    要:目的:建立测定头孢氨苄胶囊中杂质△2-头孢氨苄(杂质F)含量的方法.方法:采用HPLC法,色谱条件为:采用手性柱CHIRALPAK R AD-H柱;以0.78%磷酸二氢钠溶液(7.8g磷酸二氢钠溶于1L水中,用磷酸调pH至4.0)为流动相A和0.78%磷酸二氢钠(pH 4.0)-乙腈=55:45为流动相B;采用梯度洗脱...

关 键 词:HPLC  头孢氨苄  手性  杂质  质量

Determination of Impurity F in Cefalexin Capsules by HPLC
TANG Qiuju,XIA Sheng. Determination of Impurity F in Cefalexin Capsules by HPLC[J]. Drug Standards of China, 2020, 21(2): 124-129
Authors:TANG Qiuju  XIA Sheng
Affiliation:(Chongqing Kerui Pharmaceutical Co.,Ltd.,Chongqing 400000,China)
Abstract:Objective:To establish an HPLC method for determination ofΔ2-cefalexin(impurity F)in Cefalexin Capsules.Methods:The test was performed in a CHIRALPAKR AD-H column.0.78%sodium dihydrogen phosphate buffer(dissolve 7.8 g sodium dihydrogen phosphate with 1 L water,then adjust pH as 4.0 with phosphoric acid)was used as mobile phase A,and 0.78%sodium dihydrogen phosphate(pH 4.0)-acetonitrile(55∶45)as mobile phase B.The gradient elution procedure was used.The flow rate was 1.0 mL·min-1,and the UV detection wavelength was at 220 nm.Results:Cefalexin and impurity F were separated well under the chromatographic condition and the resolution was more than 10.0.Conclusion:The methodology validation results show that the established method can be suitable for control of impurity F in drug substance cefalexin and Cefalexin Capsules.
Keywords:HPLC  cefalexin  chirality  impurity  quality
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