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作 者:常佳伟 刘小舟[1] 李琳[1] 张照燕[1] 赵云丽[1] 于治国[1]
出 处:《沈阳药科大学学报》2018年第1期25-30,46,共7页Journal of Shenyang Pharmaceutical University
摘 要:目的建立高效液相色谱法测定氨己烯酸有关物质含量的方法。方法采用Spherisorb S5 C6色谱柱(250 mm×4.60 mm,5μm)串联Partisil-10 SCX色谱柱(250 mm×4.60 mm,10μm);乙腈为流动相A,质量浓度为1.7 g·L-1的二水·磷酸二氢钠溶液(含体积分数0.06%磷酸)为流动相B(体积比7∶93),流速为1.0 m L·min-1;检测波长为210 nm;柱温为35℃;进样量为20μL。结果氨己烯酸与有关物质A、B、E及未知杂质均能良好分离;各有关物质在线性范围内线性关系良好,r≥0.999(n=8);回收率在90%~108%内(RSD≤6%),经对三批样品测定,有关物质的含量质量分数均低于限度(0.1%)。结论建立的方法可作为氨己烯酸有关物质的测定。Objective To develop an HPLC method for determination of the related substances in the vigabatrin. Methods A Spherisorb S5 C6 column ( 250 mm × 4. 60 mm, 5 μm) tandem a Partisil-10 SCX column(250 mm × 4.60 mm, 10 m)were used with the mobile phase consist of acetonitrile-0. 17% dihydrate sodium dihydrogen phosphate solution (0. 06 % phosphoric acid) ( V: V = 7:93 ). The flow rate was 1.0 mL,min-1 and the injection volume was 20 μL. The detection wavelength was set as 210 nm and the column temperature was 35 ℃. Results All the related substances gained a completely chromatographic separation. Good linear relationships of three related substances were obtained ( r ≥0. 999 ) and recoveries were in the range of 90%- 108%. The content of the related substances in 3 batches of samples were below 0. 1%. Conclusions The established method is simple, accurate and highly sensitive and specific, and it can be applied to determine the contents of vigabatrin and related compounds.
分 类 号:R917[医药卫生—药物分析学]
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