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HPLC测定奥格列汀中基因毒性杂质残留量 被引量:2

Determination of Genotoxic Impurities in Omarigliptin by HPLC
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摘要 目的建立奥格列汀原料药中基因毒性杂质的HPLC测定方法。方法采用Zorbax SB-C18色谱柱(250 mm×4.6 mm,5μm),进样量:20μL;流动相为0.1%乙酸水-乙腈(65∶35);流速为1 m L·min^(-1);紫外检测器,检测波长为220 nm;柱温为25℃,色谱乙腈为溶剂。结果该方法专属性良好,测得苯磺酸异丙酯在4~60μg·m L-1内线性关系良好,平均回收率为98.56%(n=9,RSD=3.78%),溶液在8 h内稳定。结论该法操作简便,重复性好,结果准确可靠,可用于奥格列汀原料药中基因毒性杂质的测定。 OBJECTIVE To establish an HPLC method to determine genotoxic impurities in omarigliptin bulk drug. METHODS The HPLC was carried out with Zorbax SB-C18 column with the column temperature of 25 ℃. The injection volume was 20 μL. The mobile phase was 0.1% acetic acid water solutiom-acetonitrile(65∶35) with the flow rate of 1 m L·min^-1. The detector was UVD with the detection wave of 220 nm. Acetonitrile was used as solvent for omarigliptin. RESULTS Isopropyl benzenesulfonate could be separated completely with good linear relationship in 4-60 μg·m L-1. The average recovery of isopropyl benzenesulfonate was 98.56%(n=9, RSD=3.78%). CONCLUSION This method is simple, reproducible and accurate for determination of genotoxic impurities in omarigliptin bulk drug.
作者 郑飞 华国栋
出处 《中国现代应用药学》 CAS CSCD 2017年第3期396-398,共3页 Chinese Journal of Modern Applied Pharmacy
关键词 奥格列汀 原料药 基因毒性杂质 苯磺酸异丙酯 高效液相色谱法 omarigliptin bulk drug genotoxic impurities isopropyl benzenesulfonate HPLC
作者简介 郑飞,女,主管药师Tel:13621231026E-mail:zhengfei071@126.com 通信作者:华国栋,男,硕士,主任药师Tel:(010)67638124E-mail:zhaojhuagd@126.com
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  • 1刘梅,张琰,文爱东,杨林,李微,袁静,高晓华.苯磺酸氨氯地平片的血药浓度测定及其药动学特征[J].中国临床药学杂志,2007,16(4):211-214. 被引量:6
  • 2CDER. Guidance for industry:Genotoxic and carcinogenic impu- rities in drug substances and products: recommended approaches, 2008 : 12.
  • 3Raman. Development and validation of RP-HPLC method for the determination of genotoxic alkyl benzenesulfonates in amlodipine besylate. Journal of Pharmaceutical and Biomedical Analysis, 2008,48 : 227-230.

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