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作 者:吕应年[1] 侯英奇[2] 范世锦[3] 苟占平[1,3]
机构地区:[1]广东医学院广东天然药物研究与开发重点实验室,广东湛江524023 [2]中央司法警官学院侦查教研室,河北保定073007 [3]广东医学院药学院,广东东莞523808
出 处:《中国药房》2012年第47期4472-4474,共3页China Pharmacy
基 金:广东省科技计划项目(2009B030801336);东莞市高等院校科研机构科技计划项目(2008108101050)
摘 要:目的:建立测定刺齿凤尾蕨中抗肿瘤成分5F含量的方法,并测定其不同部位中5F的含量。方法:采用高效液相色谱法。色谱柱为HypersilC1(8250mm×4.6mm,5μm),流动相为甲醇-1%醋酸水溶液(梯度洗脱),流速为1.0mL·min-1,检测波长为242nm,柱温为30℃。结果:5F检测浓度在6~96μg·mL-1范围内与峰面积积分值呈良好线性关系(r=0.9981);低、中、高浓度对照品加入量对应的平均加样回收率分别为103.33%、100.84%、100.39%,RSD分别为5.86%、3.05%、1.02%(n均为6)。5F在刺齿凤尾蕨叶中含量最高,茎中含量其次,根中含量最低。结论:本方法稳定、快速且杂质干扰小,可用于刺齿凤尾蕨中5F的含量测定。OBJECTIVE: To establish an method for content determination of antitumor active component 5F from Pteris dispar, and to determine the content of 5F in different parts. METHODS: HPLC method was adopted. The separation was performed on Hypersil C18(250 mm×4.6 mm,5 μm)column with mobile phase consisted of methanol-1% acetic acid (gradient elution) at the flow rate of 1.0 mL·min-1. UV detection wavelength was set at 242 nm, and the column temperature was maintained at 30 ℃. RESULTS: The linear range of 5F was 6~96 μg·mL-1(r=0.998 1). The average recoveries were 103.33%,100.84% and 100.39%,and RSDs were 5.86%,3.05% and 1.02%(n=6).The content of 5F in the leaves of P. dispar was the highest,followed by the steam and root. CONCLUSION: The methods is stable,rapid and less interference from impurity, and can be used for the content determination of 5F in P. dispar.
关 键 词:刺齿凤尾蕨 抗肿瘤成分 Ent-11α-hydroxy-15-oxo-kaur-16-en-19-oic-acid(5F) 含量测定
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