Content determination of four components in Haoqin Huaban Granules by HPLC
WANG Xia1 GONG Tao1▲ SUN Liyun2 LI Tuoxin1 ZHU Qing1 SONG Jingmei1
1.Institute of Clinical Pharmacy of Beijing Municipal Health Bureau, Beijing 100035, China;
2.Dermatology, Beijing Hospital of Traditional Chinese Medicine Affilionted to Capital Medical University, Beijing 100010, China
Abstract:Objective To establish high-performance liquid chromatography (HPLC) method for the content determination of the loganic acid, gentiopicroside, paeoniflorin and 5-O-methylvisamminol in Haoqin Huaban Granules. Methods The column was Kinetex EVO C18 (150 mm × 4.6 mm, 5 μm). The mobile phase consisted of acetonitrile-0.1% phosphoric acid solution with gradient elution at the flow rate of 1.0 mL/min. The detecting wavelength was 235 nm and the column temperature was 35℃. Results The standard curve of loganic acid, gentiopicroside, paeoniflorin and 5-O-methylvisamminol were Y = 1.5×103X - 0.88 (r = 0.9999),Y = 9.8×102X - 2.95 (r = 0.9999),Y =1.4×103X - 3.97 (r = 0.9999),Y =2.4×103X - 0.33 (r = 0.9999), and the linear ranges of loganic acid, gentiopicroside, paeoniflorin and 5-O-methylvisamminol were 0.03-0.69 mg/L, 0.15-3.00 mg/L, 0.17-3.44 mg/L, 0.01-0.11 mg/L,respectively. The average recoveries of loganic acid, gentiopicroside paeoniflorin and 5-O-methylvisamminol were 97.85%, 98.30%, 94.66%, 96.08%, the RSD were 1.00%,0.69%,1.72%,1.90%, respectively. Conclusion The method is simple, accurate and reproducible. It is effective in controlling the quality of Haoqin Huaban Granules.
王夏1 龚韬1▲ 孙丽蕴2 李拓新1 朱青1 宋京美1. HPLC法测定蒿秦化斑颗粒中四种成分的含量[J]. 中国医药导报, 2019, 16(16): 28-32.
WANG Xia1 GONG Tao1▲ SUN Liyun2 LI Tuoxin1 ZHU Qing1 SONG Jingmei1. Content determination of four components in Haoqin Huaban Granules by HPLC. 中国医药导报, 2019, 16(16): 28-32.
[1] Kong M,Liu HH,Xu J,et al. Quantitative evaluation of Radix Paeoniae Alba sulfur-fumigated with different durations and purchased from herbal markets:simultaneous determination of twelve components belonging to three chemical types by improved high performance liquid chromatography [J]. J Pharm Biomed Anal,2014,98(10):424-433.
[2] Li SP,Zhao J,Yang B. Strategies for quality control of Chinese medicines [J]. J Pharm Biomed Anal,2011,55(4):802-809.
[3] 王智民,钱忠直,张启伟,等.一测多评法建立的技术指南[J].中国中药杂志,2006,12(23):657-658.
[4] 任春,武洋,王怡君,等.HPLC法测定追风透骨片中龙胆苦苷的含量[J].中国药事,2012,26(9):1003-1005.
[5] 吴立宏,叶燕,李兴尚,等.反相高效液相色谱法测定道地产区秦艽药材中龙胆苦苷的含量[J].药物分析杂志,2009,29(2):184-187.
[6] 魏舒畅,林方圆,金辉,等.复方秦艽巴布剂质量标准研究[J].中国中医药信息杂志,2011,18(5):47-49.
[7] 王化,何丹娆,朱良玉,等.HPLC法同时测定赤芍中9个活性成分的含量[J].中草药,2018,49(3):708-711.
[8] 张艳,申丽莎,杨帆,等.赤芍药材中芍药苷含量测定方法的改进[J].中国药业,2017,26(24):28-29.
[9] 鲍邢杰.赤芍的质量控制研究进展[J].广州化工,2017, 45(4):12-13.
[10] 陈述.HPLC法测定不同产地赤芍中芍药苷的含量及重金属和残留农药的分析[J].世界中医药,2014,9(9):1224-1227.
[11] 刘卉,单进军,康安,等.甘草酸和甘草次酸对芍药苷在大鼠体内药动学参数的影响[J].中草药,2013,44(12):1610-1614.
[12] 崔广智.芍药苷抗抑郁作用的实验研究[J].现代药物与临床,2009,24(4):231-233.
[13] 刘小蔓,常增荣,戴俊东,等.HPLC法同时测定牡丹皮中4种化学成分的含量[J].中国新药杂志,2015,24(8):954-957.
[14] 胡紫艳,冯振斌,蒋健,等.HPLC测定不同产地防风中4种有效成分的含量[J].中国执业药师,2016,13(11):31-34.
[15] 杨雪梅,班小军,杨海红,等.多波长HPLC梯度洗脱法同时测定保安万灵丹中升麻素苷、5-O-甲基维斯阿米醇苷-甲基维斯阿米醇苷、茅术醇、β-桉叶醇和苍术素的含量[J].药学进展,2015,39(5):384-388.
[16] 邵留英,喻志斌,瞿发林,等.不同产地防风饮片中有效成分含量比较[J].海峡药学,2013,25(2):52-54.
[17] 李悦悦,王慧,陈俊,等.HPLC法测定防风中升麻苷、升麻素、5-O-甲基维斯阿米醇苷-甲基维斯阿米醇苷和亥茅酚苷的含量[J].药学实践杂志,2010,28(6):445-447,474.
[18] 国家药典委员会.中华人民共和国药典(一部)[S].2015年版.2015:149,158,270.
[19] 黄澜,陈惠玲,李玲玲,等.HPLC同时测定正天丸中芍药苷、阿魏酸、升麻素苷、5-O-甲基维斯阿米醇苷-甲基维斯阿米醇苷的含量[J].中国中药杂志,2013,38(13):2114-2117.
[20] 陈静,李正杰,张彦芬,等.HPLC法测定痛泄胶囊中升麻素苷、5-O-甲基维斯阿米醇苷-甲基维斯阿米醇苷、芍药苷含量[J].医药信息,2011,28(4):35-37.
[21] 宋汉敏,李彦超,李宜鲜,等.HPLC同时测定养血软坚片中的马钱苷酸、龙胆苦苷和芍药苷[J].华西药学杂志,2014,29(1):79-81.
[22] 秦昆明,杨冰,胡静,等.一测多评法在中药多组分质量控制中的应用现状与思考[J].中草药,2018,49(3):725-731.
[23] Pan W,Yang L,Feng W,et al. Determination of five sesquiterpenoids in Xingnaojing injection by quantitative analysis of multiple components with a single marker [J]. J Sep Sci,2015,38(19):3313-3323.
[24] 刘晖晖,张辉,莫结丽,等.一测多评法测定黄连配方颗粒中4个成分的含量[J].中国药业,2012,21(10):39-40.
[25] 匡艳辉,朱晶晶,王智民,等.一测多评法测定黄连中小檗碱、巴马汀、黄连碱、表小檗碱、药根碱含量[J].中国中药杂志,2009,3(5):390-394.