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唑啉头孢菌素中间体(裂解物)的高效液相色谱分析

刘文英, 张胜强, 盛龙生, 安登魁

刘文英, 张胜强, 盛龙生, 安登魁. 唑啉头孢菌素中间体(裂解物)的高效液相色谱分析[J]. 中国药科大学学报, 1983, (1): 34-38.
引用本文: 刘文英, 张胜强, 盛龙生, 安登魁. 唑啉头孢菌素中间体(裂解物)的高效液相色谱分析[J]. 中国药科大学学报, 1983, (1): 34-38.
Liu Wenying, Zhang Shengqiang, Sheng Longsheng, An Dengkui. ANALYSIS OF INTERMEDIATE OF CEFAZOLIN (Cleavage Product) BY HPLC[J]. Journal of China Pharmaceutical University, 1983, (1): 34-38.
Citation: Liu Wenying, Zhang Shengqiang, Sheng Longsheng, An Dengkui. ANALYSIS OF INTERMEDIATE OF CEFAZOLIN (Cleavage Product) BY HPLC[J]. Journal of China Pharmaceutical University, 1983, (1): 34-38.

唑啉头孢菌素中间体(裂解物)的高效液相色谱分析

ANALYSIS OF INTERMEDIATE OF CEFAZOLIN (Cleavage Product) BY HPLC

  • 摘要: 本文采用YWG-NH_2色谱柱,以0.6M醋酸盐缓冲溶液为洗脱液,于紫外检测波长272nm处,用外标法或追加法,对唑啉头孢菌素中间体7-氨基-3-[2-(5-甲基-1,3,4-噻二唑)-硫甲基]-3-头孢-4-羧酸(简称裂解物)进行定量分析,两种方法的相对平均偏差为3%。方法可供生产过程中进行质量控制之用。
    Abstract: High performance liquid chromatography was employed for the quantitative determination of intermediate of cefazolin, 7-amino-3-(2-(5-methyl-1, 3, 4, thiadiazolyl) thiomethyl)- △3 cephem-4-carboxylic acid which is so called as "cleavage product". Good assay result can be obtained by using external standardization or standard addition method, on YWG-NH2 column with 0.6M acetate buffer solution as mobil phase and UV detector (at 272nrn). The average relative deviation of these two methods is 3%. The proposed method is suitable for the quality control in the process of manufacture of cefazolin.
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出版历程
  • 刊出日期:  1983-05-24

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