The server is under maintenance between 08:00 to 12:00 (GMT+08:00), and please visit
later.
We apologize for any inconvenience caused
Determination of process impurities and degradation products in Doxofylline Injection by HPLC
Author(s): LIU Xugui, HAO Yanqi, DING Shanshan
Pages: 646-
649
Year: 2016
Issue:
11
Journal: Qilu Pharmaceutical Affairs
Keyword: Doxofylline; Theophylline; HPLC; Impurity;
Abstract: Objective To establish an HPLC method for the determination of process impurities and degradation prod-ucts in Doxofylline Injection.Methods The assay was performed on an Agilent TC-C18 column(4.6 mm×250 mm,5 μm) with acetonitrile-phosphate buffer(pH 5.0)(20: 80)as mobile phase,the flow rate was 1.0 mL·min-1 ,the column tem-perature was 30 ℃ and the detection wavelength was 274 nm.Results Good linearity was obtained in 0.031~9.62,0.043~9.080 and 0.126~ 10.561 μg·mL-1 for theophylline,impurity B and inmpurity D,respectively.The correlation coefficient was at least 0.999.The average recovery rates of theophylline,impurity B and impurity D were 101.4%( RSD = 0.3%), 99.3%(RSD= 0.9%),96.6%(RSD= 1.4%),n= 9.Conclusion The method can be used for the determination of process impurities and degradation products in Doxofylline Injection with high sensitivity,accurate and reliable results.
Citations
No citation found
Related Articles
No related articles found