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作 者:黄辉庆[1] 袁小红[1,2] 周健韬[3] 胡学军[1]
机构地区:[1]广东省中医院,广东广州510120 [2]广东省中医药科学院,广东广州510006 [3]广州中医药大学,广东广州510006
出 处:《中药新药与临床药理》2015年第3期377-380,共4页Traditional Chinese Drug Research and Clinical Pharmacology
基 金:广东省中医药管理局课题(2008125);广东省科技厅课题(0903124)
摘 要:目的建立补骨脂微囊中补骨脂素和异补骨脂素的含量测定方法。方法采用高效液相色谱法,以Diamonsil(Ⅱ)-C18柱(4.6 mm×250 mm,5μm)为固定相,以甲醇:水(52∶48)为流动相,流速为1 m L·min-1,测定波长为245 nm。结果补骨脂微囊中补骨脂素含量在0.058~0.29μg之间,异补骨脂素含量在0.047~0.235μg之间线性关系良好。补骨脂素线性回归方程为:Y=211373X-649200,r=0.9998;异补骨脂素为Y=152289X-167131,r=0.9996。补骨脂微囊中补骨脂素和异补骨脂素的总含量均值为16.8 mg·g-1。结论该测定方法稳定、简便、重复性好,可以有效控制补骨脂微囊的质量。Objective To establish a method for the simultaneous determination of psoralen and isopsoralen in Fructus Psoraleae Microcapsules. Methods HPLC was carried out on the column of Diamonsil(II)-C18column(4.6 mm×250mm,5 μm). The mobile phase consisted of methanol-water(52∶48),the flow rate was 1.0 m L·min-1and the UV detection wavelength was 245 nm. Results Good linearity of psoralen was showed within the range of 0.058 ~ 0.290 μg and that of isopsoralen within the range of 0.047~0.235 μg. The equation of linear regression for psoralen was Y=211373X-649200, r=0.9998, and for isopsoralen was Y=152289X-167131, r=0.9996. The total content of psoralen and isopsoralen in the microcapsules was 16.8 mg·g-1. Conclusion The method is stable, accurate and simple,and is suitable for the quality control of Fructus Psoraleae Microcapsules.
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