|
|
Establishment of HPLC fingerprint of Jiangzhi Shuxin Mixture and detection of influencing factors of preparation safety project |
LIU Min FAN Lei CHEN Guiyun YU Le FENG Meiling |
Lishui Institute of Food and Drug & Quality and Technical Inspection, Zhejiang Province, Lishui 323000, China |
|
|
Abstract Objective To improve the quality control standard of Jiangzhi Shuxin Mixture. Methods Waters XB C18 (4.6 mm × 250 mm, 5 μm) was used as the mobile phase, and methanol was used as mobile phase A. The mixed aqueous solution (containing 0.6% phosphoric acid and 0.2% tetrahydrofuran) was used as mobile phase B. Gradient elution: 0-15 min, 2% A; 15-55 min, 2%-25% A; 55-90 min, 25%-40% A; 90-110 min, 40%-50% A. The detection wavelength was 280 nm, the column temperature was 30℃, the flow rate was 1.0 mL/mim, the analysis time was 120 min, and the injection volume was 10 μL. The above method was used to establish a fingerprint for Jiangzhi Shuxin Mixture. The content of the preservative in the preparation was determined by high performance liquid chromatography. Inductively coupled plasma mass spectrometry is used to detect heavy metals and harmful elements that may be contained. Results The similarity of 10 batches of samples met the requirements. The contents of benzoic acid were less than 0.3%. The contents of lead, cadmium, chromium, arsenic, nickel, copper and mercury in the samples all conform to the new general rule <232> of the American Pharmacopoeia. Conclusion The fingerprint established in this study is simple, reproducible and provides a scientific basis for the comprehensive quality evaluation of Jiangzhi Shuxin Mixture. It is suggested that more items affecting the safety of the preparation should be added in order to strictly control the quality of the preparation.
|
|
|
|
|
[1] 浙江省食品药品监督管理局.浙江省医疗机构制剂规范[S].2005:64.
[2] 国家药典委员会.中国药典[S].4部.北京:中国医药科技出版社,2015:26,205-207.
[3] 陆龙根.植物类中药材中砷镉和铅的含量及安全性评价[J].微量元素与健康研究,2003,20(1):53-54.
[4] 梁启超,李荣辉,刘爽.降低中药中重金属含量方法的研究进展[J].微量元素与健康研究,2012,29(2):48-50.
[5] 张珺,程月发,张爱兵.丹参胶囊水溶性成分的高效液相色谱指纹图谱分析[J].医药导报,2015,34(1):89-93.
[6] 李佩,舒成仁,刘莹,等.丹参饮片高效液相指纹图谱及其分级研究[J].湖北中医药大学学报,2015,17(5):50-54.
[7] 徐静瑶,刘小琳,佟玲,等.注射用丹参多酚酸UPLC的指纹图谱与组分分析[J].沈阳药科大学学报,2016,33(2):131-139.
[8] 杨航、尹春梅,焦连庆,等.虎杖药材的HPLC-DAD-ELSD指纹图谱研究[J].中草药,2015,46(12):1830-1835.
[9] 蔺红伟,朴淑娟,江春霞,等.虎杖饮片指纹图谱的研究及其耐用性考察[J].药学实践杂志,2016,34(2):174-187.
[10] 黎量,杨诗龙,刘玉杰,等.基于相关性分析的山楂炮制过程气味变化机制研究[J].中国中药杂志,2014,39(17):3283-3285.
[11] 胡玉珍,唐洁,熊苏慧,等.不同产地山楂与野山楂果实UPLC指纹图谱的建立及模式识别[J].中成药,2018,40(4):982-987.
[12] 黄洪新,徐道华,刘俊臣,等.地黄炮制前后5-羟甲基糠醛含量的研究[J].时珍国医国药,2012,23(4):938-939.
[13] 曹建军,梁宗锁,杨东风,等.地黄HPLC-DAD多波长指纹图谱的建立及其在熟地黄炮制中的应用[J].中草药,2014,45(2):265-270.
[14] 杨满琴,谢若男,徐玥玮,等.多产地何首乌药材质量的HPLC指纹图谱评价研究[J].广州化工,2017,45(17):96-98,113.
[15] 孙立丽,任晓亮,张慧杰,等.基于超高效液相色谱指纹图谱和化学计量学相结合的何首乌炮制研究[J].中华中医药杂志(原中国医药学报),2017,32(5):2194-2197.
[16] 王福刚,刘斌,曹娟,等.荷叶药材HPLC指纹图谱研究[J].中成药,2011,33(8):1285-1288.
[17] 丁亚平,邢少青,张成森,等.不同品种荷叶HPLC指纹图谱研究[J].天然产物研究与开发,2012,24:41-44.
[18] 陈天玲,肖雪,马晋芳.不同产地荷叶药材HPLC指纹图谱研究[J].亚太传统医药,2017,13(22):28-31.
[19] 张慧敏,余灵芝,陈旭,等.《美国药典》新通则<232>和 <233>元素杂质控制新标准和方法介绍及其对医药界的影响[J].中国药房,2014,25(17):1601-1604.
[20] 刘敏,余乐,王春春,等.妇炎愈合剂中防腐剂含量、乙醇残留量、重金属及有害元素含量的检测[J].中国药师,2017,20(10):1723-1727. |
|
|
|