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机构地区:[1]新疆维吾尔自治区药物研究所,乌鲁木齐830004
出 处:《中国药房》2013年第23期2158-2160,共3页China Pharmacy
基 金:新疆维吾尔自治区科技计划资助项目(No.201033121)
摘 要:目的:建立测定黑种草总皂苷提取物中黑种草皂苷A含量的方法。方法:采用高效液相色谱-蒸发光散射检测器(HPLC-ELSD)法。色谱柱为Cosmosil C18(250mm×4.6mm,5μm),流动相为乙腈-水(梯度洗脱),流速为1.0ml/min,柱温为30℃,进样量为10μl,ELSD的漂移管温度为65℃,气体流速为2.0L/min。结果:黑种草皂苷A的质量浓度在0.183~2.562mg/ml范围内与其峰面积积分值呈良好的线性关系(r=0.9990);精密度、稳定性、重复性试验的RSD均<2%;平均加样回收率为99.93%,RSD=1.60%(n=6)。结论:该方法操作简便、重复性好、准确性高,可用于黑种草总皂苷提取物中黑种草皂苷A的含量测定。OBJECTIVE: To establish a method for the determination of nigeglanoside A in total saponin extract of Nigella glan-dulifera. METHODS: HPLC-ELSD method was adopted. The separation was performed on Cosmosil C18(250mm×4.6mm,5μm) column with mobile phase consisted of acetonitrile-water (gradient elution) at the flow rate of 1.0 ml/min. The column temperature was 30 ℃ and injection volume was 10 μl. The drift tube temperature of ELSD was set at 65 ℃ with the flow rate of 2.0 L/rain. RESULTS: The linear range of nigeglanoside A were 0.183-2.562 mg/ml (r = 0.999 0) with an average recovery of 99.93 % (RSD=1.60%, n=6). RSDs of precision, stability and reproducibility tests were all lower than 2%. CONCLUSIONS: The method is sim-ple, reproducible and accurate, and it can be used for the content determination of nigeglanoside A in total saponin extract of N. glandulifera.
关 键 词:黑种草总皂苷提取物 黑种草皂苷A 含量测定 高效液相色谱-蒸发光散射检测器法
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