Zhao Yan-Yan, Liu Li-Yan, Han Yuan-Yuan, Li Yue-Qiu, Wang Yan, Shi Min-Jian
Experimental Center of Medicine, Hebei University, Baoding 071000, China.
Yao Xue Xue Bao. 2013 Aug;48(8):1286-91.
A simple, fast and sensitive analytical method for the simultaneous separation and detection of 18alpha-glycyrrhizinic acid, 18beta-glycyrrhizinic acid, related substance A and related substance B by RP-HPLC and drug quality standard was established. The structures of principal component isomer and related substances of raw material drug of ammonium glycyrrhizinate have been confirmed. Reference European Pharmacopoeia EP7.0 version, British Pharmacopoeia 2012 version, National Drug Standards of China (WS 1-XG-2002), domestic and international interrelated literature were referred to select the composition of mobile phase. The experimental parameters including salt concentration, pH, addition quantities of organic solvent, column temperature and flow rate were optimized. Finally, the assay was conducted on a Durashell-C18 column (250 mm x 4.6 mm, 5 microm) with 0.01 mol x mL(-1) ammonium perchlorate (add ammonia to adjust the pH value to 8.2) -methanol (48 : 52) as mobile phase at the flow rate of 0.8 mL x min(-1), and the detection wavelength was set at 254 nm. The column temperature was 50 degrees C and the injection volume was 10 microL. The MS, NMR, UV and RP-HPLC were used to confirm the structures of principal component isomer and related substances of raw material drug of ammonium glycyrrhizinate. Under the optimized separation conditions, the calibration curves of 18 alpha-glycyrrhizinic acid, 18beta-glycyrrhizinic acid, related substance A and related substance B showed good linearity within the concentration of 0.50-100 microg x mL(-1) (r = 0.999 9). The detection limits for 18alpha-glycyrrhizinic acid, 18beta-glycyrrhizinic acid, related substance A and related substance B were 0.15, 0.10, 0.10, 0.15 microg x mL(-1) respectively. The method is sensitive, reproducible and the results are accurate and reliable. It can be used for chiral resolution of 18alpha-glycyrrhizinic acid, 18Pbeta-glycyrrhizinic acid, and detection content of principal component and related substances of raw material drug of ammonium glycyrrhizinate. It is concluded that the separation of principal component isomer of raw material drug of ammonium glycyrrhizinate and the validity of the substance's structure assignments of retention time being 1.2 in the European pharmacopoeia EP7.0 version, British pharmacopoeia 2012 version remains open to question. It may be of practical value for the quality control of raw material drug, preparation, and Chinese herbal medicine of ammonium glycyrrhizinate.
建立了一种采用反相高效液相色谱法(RP-HPLC)同时分离检测18α-甘草酸、18β-甘草酸、有关物质A和有关物质B的简单、快速、灵敏的分析方法及药品质量标准。对甘草酸铵原料药的主成分异构体及有关物质的结构进行了确证。参考欧洲药典EP7.0版、英国药典2012版、中国国家药品标准(WS 1-XG-2002)以及国内外相关文献来选择流动相的组成。对盐浓度、pH值、有机溶剂加入量、柱温、流速等实验参数进行了优化。最终,采用Durashell-C18色谱柱(250 mm×4.6 mm,5μm),以0.01 mol·mL⁻¹高氯酸铵(加氨水调节pH值至8.2)-甲醇(48∶52)为流动相,流速为0.8 mL·min⁻¹,检测波长设定为254 nm,柱温为50℃,进样量为10μL进行测定。采用质谱、核磁共振、紫外光谱及RP-HPLC对甘草酸铵原料药的主成分异构体及有关物质的结构进行确证。在优化的分离条件下,18α-甘草酸、18β-甘草酸、有关物质A和有关物质B在0.50 - 100μg·mL⁻¹浓度范围内校准曲线线性良好(r = 0.999 9)。18α-甘草酸、18β-甘草酸、有关物质A和有关物质B的检测限分别为0.15、0.10、0.10、0.15μg·mL⁻¹。该方法灵敏、重现性好,结果准确可靠。可用于18α-甘草酸、18β-甘草酸的手性拆分以及甘草酸铵原料药主成分及有关物质的含量测定。结论是甘草酸铵原料药主成分异构体的分离以及欧洲药典EP7.0版、英国药典2012版中保留时间为1.2的物质结构归属的有效性仍存在疑问。该方法对甘草酸铵原料药、制剂及中药材的质量控制可能具有实际价值。