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作 者:马晓黎[1] 李直[1] 李波[1] MA Xiaoli;LI Zhi;LI Bo(Antibiotic's Research and Re-evaluation Key Lab.of Sichuan Province,Sichuan Industrial blstitute of Antibiotics Chengdu University,Chengdu 610052)
机构地区:[1]抗生素研究与再评价四川省重点实验室,四川抗菌素工业研究所,成都大学,四川成都610052
出 处:《中国医药工业杂志》2018年第10期1440-1445,共6页Chinese Journal of Pharmaceuticals
摘 要:建立了高效液相色谱法对门冬氨酸鸟氨酸注射液进行有关物质检查。使用氨基色谱柱,以0.05 mol/L磷酸二氢钾溶液(pH 5.5)∶乙腈(47∶53)为流动相,检测波长210 nm。注射液中门冬氨酸、鸟氨酸及其主要杂质L-鸟氨酸内酰胺和富马酸分别在1.07~21.32、1.06~21.18、0.02~48.31和0.01~2.94μg/ml范围内线性关系良好,检测限分别为0.53、0.53、0.004和0.002μg/ml。主要有关物质L-鸟氨酸内酰胺和富马酸的回收率为100.74%和101.44%,RSD值均小于2%。本研究所建方法准确、稳定,分离效率更好,更适合该品种注射液的有关物质检查。An HPLC method was established for the determination of the related substances in ornithine asparate injections. An amino column was used, with the mobile phase of 0.05 mol/L potassium dihydrogen phosphate solution (pH 5.5)∶acetonitrile (47∶53), at the detection wavelength of 210 nm. The calibration curves of ornithine, aspartic acid, L-ornithine lactam and fumaric acid were linear in the ranges of 1.07-21.32, 1.06-21.18, 0.02-48.31 and 0.01-2.94 μg/ml. Their limits of detection were 0.53, 0.53, 0.004 and 0.002 μg/ml, respectively. The recoveries of the main known impurities L-ornithine lactam and fumaric acid were 100.74% and 101.44%, with RSDs less than 2%. The method established in our work is accurate and stable, with better separation efficiency, which is more suitable for the determination of the related substances in ornithine asparate injections.
关 键 词:门冬氨酸鸟氨酸 高效液相色谱 有关物质 L-鸟氨酸内酰胺 富马酸 含量测定
分 类 号:R917[医药卫生—药物分析学]
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