• 首页期刊简介编委会刊物订阅专栏专刊电子刊学术动态联系我们English
引用本文:雷蓉,刘亚茹,赵振霞,刘永利.基于UPLC-MS /MS 法的参麦颗粒中麦冬掺伪检查方法研究[J].中国现代应用药学,2025,42(8):134-139.
leirong,liuyaru,zhaozhenxia,liuyongli.Study on the adulteration of Ophiopogon Radix in Shenmai Granules based on UPLC-MS/MSLEI Rong,LIU Ya-ru,Zhao Zhen-xia,LIU Yong-li*(Hebei Institute for Drug and Medical Device Control, Hebei Key Laboratory of quality evaluation and standard of traditional Chinese Medicine,Shijiazhuang050227,China)[J].Chin J Mod Appl Pharm(中国现代应用药学),2025,42(8):134-139.
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  【EndNote】   【RefMan】   【BibTex】
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 28次   下载 16 本文二维码信息
码上扫一扫!
分享到: 微信 更多
基于UPLC-MS /MS 法的参麦颗粒中麦冬掺伪检查方法研究
雷蓉, 刘亚茹, 赵振霞, 刘永利
河北省药品医疗器械检验研究院
摘要:
目的 建立超高效液相色谱-三重四极杆质谱(UPLC-MS/MS)的参麦颗粒中麦冬掺伪检查方法,考察生产企业是否存在山麦冬掺伪麦冬投料情况。方法 以山麦冬中特征成分短葶山麦冬皂苷C、山麦冬皂苷B为检测指标,分析采用Shimadzu Shim-pack gist C18(2.1×100mm,2μm) 色谱柱,以0.1%甲酸水溶液-乙腈为流动相等度洗脱,体积流量为 0.3 mL.min-1,柱温 40 ℃。电喷雾正离子源(ESI+)扫描,多反应监测(MRM)模式。结果 短葶山麦冬皂苷C、山麦冬皂苷B分别在3.290~315.8n ng.mL-12.390~305.9 ng.mL-1呈良好的线性关系,相关系数均大于 0.9996,加样回收率为105.3%、100.6%,精密度、重复性和稳定性的RSD均小于3.0%。85批参麦颗粒样品中有8批检出山麦冬皂苷B,检出率为9.4%。结论 建立的方法简便快速、准确性好、专属性强,可用于筛查参麦颗粒中麦冬的掺伪情况。
关键词:  参麦颗粒  麦冬  山麦冬  山麦冬皂苷B  短葶山麦冬皂苷C  
DOI:
分类号:R284.1;R917.101
基金项目:
Study on the adulteration of Ophiopogon Radix in Shenmai Granules based on UPLC-MS/MSLEI Rong,LIU Ya-ru,Zhao Zhen-xia,LIU Yong-li*(Hebei Institute for Drug and Medical Device Control, Hebei Key Laboratory of quality evaluation and standard of traditional Chinese Medicine,Shijiazhuang050227,China)
leirong, liuyaru, zhaozhenxia, liuyongli
Hebei Institute for Drug and Medical Device Control
Abstract:
OBJECTIVE To establish a method for the adulteration of Ophiopogonis Radix in Shenmai Granules to investigate whether there is a phenomenon of using Liriope Radix to replace Ophiopogon Radix in the manufacture enterprises. METHODS The characteristic components liriope muscari baily saponins C and liriopesides B were used as the detection index of Liriope Radix. The sample extract was cleaned up by a C18 solid-phase extraction cartridge combined with UPLC-MS/MS. Separation was performed on a Waters Acquity BEH C18 (2.1 mm×100 mm, 1.7 μm) with a gradient elution of acetonitrile and 0.1% formic acid at the flow rate was set at 0.3 mL·min-1 and a column temperature of 40 ℃. The detection mode was Multi reaction monitoring (MRM) in electrospray positive ion source (ESI+). RESULTS Liriope muscari baily saponins C and liriopesides B showed good linearity in the range of 3.290~315.8n ng·mL-1 and 2.390~305.9 ng·mL-1, with the correlation coefficients greater than 0.9996, and the recoveries of 105.3% and 100.6%, and the RSDs of precision, reproducibility, and stability were less than 3.0%. 85 batches of Shenmai Granules contained 8 batches with the detection rate of 9.4%. CONCLUSION The established method is simple, rapid, accurate and exclusive, and can be used to screen the adulteration of Ophiopogon japonicus in Shenmai granules
Key words:  Shenmai Granules  Ophiopogon japonicus  Liriope  Liriopesides B  Liriope muscari baily saponins C  
扫一扫关注本刊微信