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Content determination of chlorogenic acid in traditional Chinese medicine and their preparations by quantitative analysis of multi-components by single marker |
ZHANG Qiuyan1 ZHANG Ni1 ZHANG Chunli2 GUO Wenquan2 CUI Hanming1 |
1.Chinese Medicine Research and Development Center, Guang′anmen Hospital, China Academy of Chinese Medical Sciences, Beijing 100053, China;
2.Shaanxi Made All the Pharmaceutical Co., Ltd, Shaanxi Province, Xianyang 712000, China |
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Abstract Objective To establish the quantitative analysis of multi-components by single marker (QAMS) method for the analysis of six chlorogenic acids in traditional Chinese medicine and their preparations. Methods A high performance liquid chromatography-photodiode array detector (HPLC-DAD) method was developed with acetonitrile-0.4% phosphoric acid as mobile phase ingradient elution. The column temperature was 25℃. The flow rare was 1.0 mL/min and the detection wavelength was 327 nm. Then the relative correction factors among the other five chlorogenic acids were calculated, when the chlorogenic acid was used as internal referring substances. The ruggedness of relative correction factors was evaluated to establish the QAMS method, when the chlorogenic acid was used as internal referring substances. The content of chlorogenic acid in traditional Chinese medicine (Lonicerae Japonicae Flos and Chrysanthemi Indici Flos) and their eye drops were calculated by the established QAMS method and external standard method respectively, and the content difference of different algorithms was analyzed by t-test and relative error analysis to evaluate the accuracy of the QAMS method. The relative retention time method was used to accurately locate the chromatographic peaks of the six constituents. Results The established relative correction factor with chlorogenic acid as internal referring substances had good ruggedness. Two methods were used to calculate the content of chlorogenic acid in 10 batches of eye drops and three batches of Lonicerae Japonicae Flos and Chrysanthemi Indici Flos. The relative error range was -3.32% to 4.99%, and there was no statistically significant difference (P > 0.05). Conclusion A rapid, accurate and convenient QAMS method for simultaneous measurement of six chlorogenic acids has been established, and this method can be used for quality analysis of six chlorogenic acids in Lonicerae Japonicae Flos, Chrysanthemi Indici Flos and their eye drops.
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[1] 那龚雪,张文涛,谈远锋,等.绿原酸及其异构体药理作用及不良反应研究进展[J].辽宁中医药大学学报,2018, 20(3):140-143.
[2] Miao M,Xiang L. Pharmacological action and potential targets of chlorogenic acid [J]. Adv Pharmacol,2020,87:71-88.
[3] 杨玉彬,柯斌,秦鉴.绿原酸对3T3-L1前脂肪细胞分化的抑制作用[J].中成药,2018,40(11):2380-2385.
[4] 严永旺,肖兰,周旭,等.绿原酸的药理作用及药用研发对策[J].中国药房,2017,28(19):2729-2732.
[5] Bagdas D,Gul Z,Meade JA,et al. Pharmacologic overview of chlorogenic acid and its metabolites in chronic pain and inflammation [J]. Curr Neuropharmacol,2020,18(3):216-228.
[6] 蒋杰,李雪营,魏学军.杜仲不同“发汗”加工方法制品中绿原酸含量的比较[J].中国民族民间医药,2019,28(1):28-30.
[7] 潘明飞,杨晶莹,李睿,等.药食同源食品金银花中绿原酸标准物质的研制与评价[J].中国食品学报,2020 20(4):224-232.
[8] 郭满满,肖卓炳,于华忠,等.热重法研究绿原酸的热稳定性、分解动力学及贮存期[J].药物评价研究,2011,34(5):348-352.
[9] 罗奇志,王有志,罗佳波.绿原酸水解产物的高效液相色谱-电喷雾串联质谱分析[J].药物分析杂志,2011,31(7):1345-1349.
[10] 顾丽红,朱品业.日光和温度对绿原酸供试液稳定性的影响[J].中成药,1999,21(11):568-569.
[11] 刘意,曾桂先,宋凤兰,等.绿原酸稳定性研究[J].化工中间体,2009,5(2):25-28.
[12] Farah A,Monteiro M,Donangelo CM,et al. Chlorogenic acids from green coffee extract are highly bioavailable in humans [J]. J Nutr,2008,138(12):2309-2315.
[13] 荣传兰,孟勇,刘丹.HPLC法同时测定多花蒿中绿原酸类成分的含量[J].中医药导报,2018,24(8):68-70.
[14] 张荣林,林雀跃.超高效液相色谱法测定清咽糖中6种绿原酸类化合物的含量[J].食品安全质量检测学报,2019(16):279-285.
[15] 伍涛,李茂婷,邓余,等.银黄-聚乙烯醇注射液稳定性研究[J].福建农业科技,2019(11):59-53.
[16] 王智民,高慧敏,付雪涛,等.“一测多评”法中药质量评价模式方法学研究[J].中国中药杂志,2006,31(23):1925-1928.
[17] 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,2011,36(6):656-658.
[18] 邱喜龙,任晓亮,张慧杰,等.热毒宁注射液中绿原酸的降解动力学研究[J].药物分析杂志,2012,32(12):2240-2245.
[19] 李建晨,廖明丽,贾玉捷,等.双黄连口服液中绿原酸含量的影响因素研究[J].河北科技大学学报,2015,36(5):499-503.
[20] Ma YC,Wang XQ,Hou FF,et al. Rapid resolution liquid chromatography(RRLC)analysis and studies on the stability of Shuang-Huang-Lian preparations [J]. J Pharmaceut Biomed,2011,54(2):265-272. |
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