ZHUANG He-fei, MENG Xia, YUAN Yang, et al. HPLC Method with Correction Factor for Determination of Content of Related Substances in Compound Omeprazole Chewable Tablet[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(9): 131-135.
ZHUANG He-fei, MENG Xia, YUAN Yang, et al. HPLC Method with Correction Factor for Determination of Content of Related Substances in Compound Omeprazole Chewable Tablet[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(9): 131-135. DOI: 10.11653/syfj2013090131.
加校正因子的主成分自身对照法测定复方奥美拉唑咀嚼片中有关物质的含量
摘要
目的: 建立加校正因子的主成分自身对照法测定复方奥美拉唑咀嚼片中有关物质的含量。 方法: Agilent XDB C8色谱柱(4.6 mm×150 mm
Objective: The self contrast and correction factor method was established to determine the content of the related substances in Compound Omeprazole Chewable Tablet. Method: Chromatography was carried out by reversed-phase technique on an Agilent XDB C8 column (4.6 mm×150 mm
5 μm) with a mobile phase composed of 0.01 mol·L-1 disodium hydrogen phosphate (adjusted to pH 7.6 with phosphate acid) and acetonitrile in the ratio of (75: 25) pumped at a flow-rate of 1.0 mL·min-1. The detection was carried out at 280 nm and a column temperature of 35℃. The injection volume was 20 μL. The slope of linear equation was used to determine the correction factor between impurity A
B
C
D
E and omeprazole. The relative retention time was used to determine the position of impurities. Result: The relative retention time between impurity A
B
C
D
E and Omeprazole was 0.3
0.9
3.4
0.8 and 0.4
respectively. The correction factor of impurity A
B
C
D
E was 1.45
0.66
1.21
1.39 and 0.80
respectively. The content of impurity D was 0.023% in three batches of samples. Other impurities weren't detected. Conclusion: The method was simple
efficient and accurate for analyzing the related substances in Compound Omeprazole Chewable Tablet.