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引用本文:邓毅,宁红霞,沈薇,石晓峰,李师,雷艳萍.HPLC同时测定雪松松针中没食子酸、原儿茶酸和儿茶素的含量[J].中国现代应用药学,2014,31(9):1104-1107.
DENG Yi,NING Hongxia,SHEN Wei,SHI Xiaofeng,LI Shi,LEI Yanping.Simultaneous Determination of Gallic Acid, Protocatechuic Acid and Catechin in Pine Needles of Cedrus Deodara by HPLC[J].Chin J Mod Appl Pharm(中国现代应用药学),2014,31(9):1104-1107.
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HPLC同时测定雪松松针中没食子酸、原儿茶酸和儿茶素的含量
邓毅1, 宁红霞1, 沈薇2, 石晓峰1,2, 李师1, 雷艳萍1
1.甘肃中医学院药学院,兰州 730030;2.甘肃省医学科学研究院药物研究所,兰州 730050
摘要:
目的 建立同时测定雪松松针中没食子酸、原儿茶酸和儿茶素含量的高效液相色谱法。方法 采用TC-C18(250 mm× 4.6 mm,5 μm)色谱柱,流动相为甲醇(A)-0.2%磷酸水溶液(B)梯度洗脱(0~8 min,10%A,8~45 min,10%→30%A),流速:1.0 mL·min-1,检测波长:280 nm,柱温:25 ℃。结果 雪松松针中没食子酸、原儿茶酸和儿茶素依次在0.4~4.0,4~40和2~20 μg·mL-1内呈良好线性关系,相关系数r分别为0.999 8,0.999 9,0.999 9,加样回收率(n=9)分别为104.7%,99.5%和105.8%。结论 该方法适用于雪松松针中没食子酸、原儿茶酸和儿茶素的含量测定,方法简单、快速、高效。
关键词:  雪松松针  没食子酸  原儿茶酸  儿茶素  含量测定  高效液相色谱法
DOI:
分类号:
基金项目:甘肃省科技支撑计划项目(1204FKCA152);甘肃省高校中(藏)药化学与质量研究省级重点实验室开放基金项目(zzy-2011-05);甘肃省卫生厅中医药科研项目(GZK-2012-29)
Simultaneous Determination of Gallic Acid, Protocatechuic Acid and Catechin in Pine Needles of Cedrus Deodara by HPLC
DENG Yi1, NING Hongxia1, SHEN Wei2, SHI Xiaofeng1,2, LI Shi1, LEI Yanping1
1.Pharmacy School of Gansu University of TCM, Lanzhou 730030, China;2.Institute of Materia Medica, Gansu Academy of Medical Science, Lanzhou 730050, China
Abstract:
OBJECTIVE To develop an HPLC method for simultaneous determination of gallic acid, protocatechuic acid and catechin components in pine needles of Cedrus deodara. METHODS Agilent TC-C18 column (250 mm×4.6 mm, 5 μm) was adopted. The mobile phase was methanol (A)-0.2% phosphoric acid (B) with gradient elution (0-8 min, 10%A; 8-45 min, 10%→30%A) at the flow rate of 1.0 mL·min-1. The column temperature was 25 ℃ and the detection wavelength was 280 nm. RESULTS Calibration curves were found to be linear in the ranges of 0.4-4.0 μg·mL-1 for gallic acid, 4-40 μg·mL-1 for protocatechuic acid and 2-20 μg·mL-1 for catechin. The correlation coefficients were 0.999 8, 0.999 9, 0.999 9. The average recoveries(n=9) of gallic acid, protocatechuic acid and catechin were 104.7%, 99.5% and 105.8%. CONCLUSION The method is simple, rapid and efficient, which is suitable for the determination of gallic acid, protocatechuic acid and catechin components in pine needles of Cedrus deodara.
Key words:  pine needles of Cedrus deodara  gallic acid  protocatechuic acid  catechin  contents determination  HPLC
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