首页|固相萃取-液相色谱法测定减肥茶中番泻苷A、番泻苷B的含量

固相萃取-液相色谱法测定减肥茶中番泻苷A、番泻苷B的含量

Determination of sennoside a and sennoside B in weight-reducing tea by solid phase extraction combined with HPLC

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目的 建立固相萃取(solid phase extraction,SPE)-液相色谱法(high performance liquid chro-matography,HPLC)测定减肥茶中番泻苷A、番泻苷B含量的方法.方法 样品经体积分数为70%的甲醇超声提取后,通过阴离子固相萃取小柱净化后,用体积分数2%氨水甲醇洗脱,洗脱液氮吹浓缩后得供试液,采用BDS HYPERSIL C18色谱柱分离,以甲醇-体积分数0.1%磷酸为流动相进行梯度洗脱,经二极管阵列检测器分析,外标法定量.结果 番泻苷A和番泻苷B在1~100 μg·mL-1质量浓度范围内线性良好,平均加标回收率为92.2%~98.4%(n=6);RSD为0.8%~3.3%(n=6).结论 本方法适用于减肥茶中番泻苷A、番泻苷B含量的检测.
Objective An analytical method based on solid phase extraction combined with high performance liquid chromatography was established for the determination of Sennoside A and Sennoside Bin weight-reducing tea.Methods After supersonic extractionwith 70%(volume fraction)methanolas solvate,the extracts were purified by anion-exchange solid phase column chromatography,eluted with methanol containing 2%(volume fraction)ammonia,and concentrated in a stream of nitrogen to obtain the final sample solutions.These samples were separated with a BDS HYPERSIL C18 chromatographic column,using methanol and 0.1%phosphoric acid(volume fraction)as the mobile phase,analyzed using a diode array detector and quantified with reference to an external standard.Results Sennoside A and SennosideBhad good linearity in the mass concentration range of 1-100 μg·mL-1,quantitative limits were 10 mg·100 g-1.The average recoveries were in the range from 92.2%to 98.4%(n=6),relative standard deviations were in the range of0.8%-3.3%(n=6).Conclusion This method accordingly proved to be suitable for the determination of Sennoside A and Sennoside Bin weight-reducing tea.

solid phase extractionHPLCweight-reducing teaSennoside ASennoside B

黄媛

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辽宁省检验检测认证中心,辽宁沈阳 110033

固相萃取 高效液相色谱法 减肥茶 番泻苷A 番泻苷B

2024

沈阳药科大学学报
沈阳药科大学

沈阳药科大学学报

CSTPCD
影响因子:0.604
ISSN:1006-2858
年,卷(期):2024.41(2)
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