1.Department of Analytical Chemistry, China Pharmaceutical University, Nanjing 210009,China;2.Producivity Promotion Center, Administrative Committee of Changzhou High-Tech Industrial Development Zone, Changzhou 213022,China
OBJECTIVE To develop HPLC and nonaqueous acid-base titration for the determination of nifekalant hydrochloride and its related substances for quality control.METHODS Chromatography was carried out on a Shimadzu CLC-ODS column (6 mm×150 mm,5 μm), using the mobile phase of acetonitrile-0.02 mol·L-1 phosphate buffer(pH 5.0 adjusted by sodium hydroxide solution 25∶75) at a flow rate of 1.0 mL·min-1. The ultraviolet detection wavelength was set at 268 nm,the column temperature was 30 ℃. RESULTS Under the established chromatographic conditions,nifekalant hydrochloride and the related substances were separated completely.The method was validated, and stability tests under various conditions were performed.The standard curve was linear within the range of 5~100 mg·L-1 with the correlation coefficient of 0.999 9, the limit of detection was 0.2 ng. CONCLUSION The established methods were simple, accurate,specific and could be used for quality control of nifekalant hydrochloride.
WU Ning;CHEN To;PENG Shui-fng;HU Chen-xi;QIO Shu-xi;SHEN Wei-yng.
Determination of Nifekalant Hydrochloride and Its Related Substances by HPLC and Nonaqueous Acid-Base Titration [J]. Chinese Pharmaceutical Journal, 2007, 42(22): 1741-1744
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