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作 者:颜海弟 谭丽容[2] 陈越 何景进[2] 李楚文[2] 吴典伟[2] 苏子仁[2]
机构地区:[1]广东省湛江市第二人民医院,广东湛江524008 [2]广州中医药大学,广州510006
出 处:《中国医院用药评价与分析》2012年第10期924-926,共3页Evaluation and Analysis of Drug-use in Hospitals of China
摘 要:目的:建立高效液相色谱(HPLC)法测定参芪补气片中黄芪甲苷的含量。方法:以吡啶∶苯甲酰氯(2∶1)为衍生化试剂,对黄芪甲苷进行苯甲酰化,采用HPLC法在270 nm波长处测定参芪补气片中黄芪甲苷的含量。结果:黄芪甲苷进样量在0.078~0.975μg范围内线性关系良好(r=0.999 9),重复性好(RSD=0.82%),回收率平均值为99.51%~100.76%(RSD=0.29%~1.11%)。结论:该法样品前处理简单、专属性强、准确度高、灵敏度高、重现性好,可以作为控制参芪补气片中黄芪甲苷质量的方法。OBJECTIVE: To establish HPLC determination of astragaloside Ⅳ in Shenqi Buqi tablets.METHODS: By using pyridine-benzoyl chloride(2∶1) as derivatization reagents for benzoylation of astragaloside Ⅳ.The content of Astragaloside Ⅳ in Shenqi Buqi tablets was determined by HPLC at a wavelength of 270 nm.RESUTLS: The linear range of astragaloside Ⅳ was 0.078-0.975 μg(r=0.999 9).The method had good reproducibility(RSD=0.82%) with average recovery rate of 99.51%-100.76%(RSD=0.29%-1.11%).CONCLUSION: The method is simple in pretreatment of samples,specific,accurate,sensitive and reproducible,thus it can be used for the quality control of astragaloside Ⅳ in Shenqi Buqi tablets.
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