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RP-HPLC法测定补肾强身片中金丝桃苷的含量 被引量:8

Content Determination of Hyperoside in Bushen Qiangshen Tablets by RP-HPLC
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摘要 目的:建立测定补肾强身片中金丝桃苷含量的方法。方法:采用反相高效液相色谱法。色谱柱为Amethyst C18-H,流动相为乙腈-0.1%磷酸溶液(16∶84,V/V),流速为1.0 ml/min,柱温为30℃,检测波长为360 nm,进样量为10μl。结果:金丝桃苷的进样量在0.061 0~1.220 4μg范围内与其峰面积积分值呈良好的线性关系(r=0.999 9);精密度、稳定性、重复性试验的RSD≤0.52%;平均加样回收率为98.68%,RSD为0.64%(n=6)。结论:本方法快速、简便,结果准确、可靠,可用于补肾强身片的含量测定。 OBJECTIVE: To establish a method for the content determination of hyperoside in Bushen qiangshen tablets. METHODS: RP-HPLC method was adopted. The determination was performed on Amethyst C18-H cohman with mobile phase consisted of acetonitrile-0.1% phosphoric acid solution (16:84, V/V) at the flow rate of 1.0 ml/min. The column temperature was 30 ℃, and the detection wavelength was set at 360 nm,the sample size was 10 μl. RESULTS: The linear range of hyperoside were 0.061 0-1.220 4 μg(r=0.999 9)with an average recovery of 98.68% (RSD=0.64% ,n=6). RSDs of precision, reproducibility and stability tests were lower than 0.52%. CONCLUSIONS: This method is accurate, rapid, simple and reliable. It can be used for the content determination of Bushen qiangshen tablets.
出处 《中国药房》 CAS 北大核心 2015年第3期413-415,共3页 China Pharmacy
关键词 反相高效液相色谱法 补肾强身片 金丝桃苷 含量测定 RP-HPLC Bushen qiangshen tablets Hyperoside Content determination
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