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Quality standard for Ma′nao Gao |
LI Xiaojing1 WEI Yingjie1,2 WANG Jing1,2 XU Huan1 HUANG Yiping1,2 Janagul·As3 CHEN Bin1,2 |
1.The Third Clinical Medical College, Nanjing University of Chinese Medicine, Jiangsu Province, Nanjing 210028, China;
2.Key Laboratory for Traditional Chinese Medicine Drug Release System Under State Administration of Traditional Chinese Medicine, Jiangsu Province Academy of Traditional Chinese Medicine, Jiangsu Province, Nanjing 210028, China;
3.Xinjiang Yili Kazak Autonomous Prefecture Hospital of Traditional Chinese Medicine, Xinjiang Uygur Autonomous Region, Yining 835000, China |
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Abstract Objective To establish a quality control method for Ma′nao Gao. Methods Thin layer chromatography was applied to the qualitative identification of Faeces Togopteri, Corydalis Rhizoma, Rhei Radix et Rhizoma, Psoraleae Fructus, Notoginseng Radix et Rhizoma. High performance liquid chromatography was used for the content determination of tetrahydropalmatine, acetonitrile-0.1% triethylamine phosphate system was used as the mobile phase of gradient elute. The column temperature was 30°C and the detection wavelength was set at 280 nm. Results Thin layer chromatography spots was clear, which had good resolution without interference. Tetrahydropalmatine had good linear relationship with the range of 2.022-20.22 μg/mL (r = 0.9999) respectively, the average recovery was 100.27% (RSD = 2.39%). Conclusion The method is reliable with good stability and good repeatability, and can be used for quality control of Ma′nao Gao.
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[1] 江阿古丽,吾古丽汗,康雄,等.哈萨克药玛瑙膏抗炎镇痛作用的实验研究[J].中国民族医药杂志,2006(2):28-29.
[2] 江阿古丽·艾山,江安努尔·这依肯,古丽孜哈·哈布什,等.玛瑙膏外敷治疗骨与软组织损伤的临床研究[C]//2016《中国组织化学与细胞化学》杂志临床研究研讨会论文汇编,2016.
[3] 陕西省食品药品监督管理局.陕西省药材标准[M].西安:陕西科学技术出版社,2015.
[4] 国家药典委员会.中国药典[S].一部.北京:中国医药科技出版社,2015.
[5] 程巧鸳,郑成,郑瑜倩,等.小儿热速清颗粒质量标准研究[J].医药导报,2017,36(3):321-325.
[6] 吴小斌.三黄益肾颗粒的药学研究[D].广州:广州中医药大学,2017.
[7] 曹建华.用硅胶G板对健儿强身膏中的补骨脂﹑陈皮﹑续断进行薄层色谱鉴别的价值[J].当代医药论丛,2019, 17(3):197-199.
[8] 李祥溦,吕新林,李紫阳,等.盐补骨脂饮片标准汤剂分析研究[J].中国中药杂志,2019,44(10):2078-2083.
[9] 李万红.五藤胶囊的薄层色谱定性鉴别及其补骨脂素HPLC定量研究[J].西部中医药,2015,28(6):25-29.
[10] 温馨,江耀伦,陈素珍,等.大七厘散中大黄及当归薄层色谱鉴别方法改进[J].中国药业,2017,26(14):7-9.
[11] 赵振霞,王敏,王钰宁,等.心可舒丸中三七的薄层色谱鉴别和6种物质的含量测定[J].华西药学杂志,2016, 31(6):656-659.
[12] 张红星.红花接骨丸中三七、血竭薄层色谱鉴别研究[J].中国民族民间医药,2013,22(9):13.
[13] 陈娇.三七跌打损伤软膏的药学研究[D].成都:成都中医药大学,2017.
[14] 张丹,王昌利,卜雕雕,等.高效液相色谱法同时测定延胡索中5种生物碱含量的方法学研究[J].中南药学,2018, 16(12):1759-1762.
[15] 邓磊,和明伟,侯连兵.HPLC-CAD法同时测定元胡止痛胶囊中6种生物碱及香豆素类成分的含量[J].中南药学,2019,17(1):88-92.
[16] 胡锦祥,吴瑾瑾,王群星,等.大孔吸附树脂纯化延胡索总生物碱工艺研究[J].中草药,2018,49(18):4302-4310.
[17] 任彬.UPLC法测定木丹颗粒中延胡索乙素的含量[J].海峡药学,2018,30(10):54-56.
[18] 吴芸,陈志鹏,肖璐,等.延胡索乙素平衡溶解度及表观油水分配系数的测定[J].南京中医药大学学报,2012, 28(2):178-180.
[19] 徐汇,霍艳萍,高晓艳.HPLC法测定腰痹通胶囊中延胡索乙素的含量[J].世界最新医学信息文摘,2017,17(83):72-73.
[20] 黄涛,刘丽,张笑敏,等.夏天无HPLC指纹图谱及多指标含量测定研究[J].中草药,2019,50(10):2474-2479.
[21] 王欢,毕福钧,林彤,等.延胡索HPLC指纹图谱研究及9种生物碱含量测定[J].中药材,2017,40(3):624-629.
[22] 吕子明,刘文娟,于向红,等.大孔吸附树脂纯化延胡索总生物碱工艺研究[J].中国医药导报,2012,9(20):109-112. |
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