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作 者:陈伟康 朱艳艳 刘德鸿 杨毅生 CHEN Weikang;ZHU Yanyan;LIU Dehong;YANG Yisheng(Jiangxi Institute for Drug Control,NMPA Key Laboratory of Quality Evaluation of Traditional Chinese Patent Medicine,Jiangxi Province Engineering Research Center of Drug and Medical Device Quality,Nanchang 330029;Jiangxi University of Chinese Medicine,Nanchang 330004)
机构地区:[1]江西省药品检验检测研究院,国家药品监督管理局中成药质量评价重点实验室,江西省药品与医疗器械质量工程技术研究中心,江西南昌330029 [2]江西中医药大学,江西南昌330004
出 处:《分析科学学报》2024年第5期587-591,共5页Journal of Analytical Science
基 金:江西省重点研发计划项目(20212BBG73025);江西省药品监督管理局科研项目(2021KY44)。
摘 要:建立了超高效液相色谱-串联质谱检测枳实药材中辛弗林、N-甲基酪胺的方法。以甲醇为提取溶剂,经QuECHERS分散净化,采用资生堂CAPCELL PAK CR色谱柱(150mm×2.0mm,5μm;C_(18)和SCX比例为1∶4)分离,质谱以正离子扫描,反应监测模式测定。辛弗林和N-甲基酪胺在10~2000ng/mL范围内线性关系良好(R^(2)>0.997),检出限和定量限分别为0.3ng/mL和1.0ng/mL,回收率范围为94.3%~105.7%,相对标准偏差(RSD)均小于3%。该方法避免了使用磷酸盐和离子对试剂,仅在流动相中添加甲酸和甲酸铵,分析物就能有较好的保留,具有极高的质谱响应。相较于传统方法,该方法分析时间短、操作简单、专属性强,在强极性生物碱分离检测方面具有较好的应用价值。An ultra performance liquid chromatographytriple quadrupole mass spectrometry(UPLCMS/MS)method for the determination of synephrine and nmethyl tyramine in Frutus Aurantii Immaturus was established.The samples were extracted with methanol,and purified by QuECHERS.The separation was performed on Shiseido CAPCELL PAK CR column(2.0 mm×150 mm,5μm;C_(18)to SCX ratio of 1:4),and the samples were determined by positive ion scanning with multireaction monitoring mode.The linear relationship of synephrine and nmethyl tyramine was good in the range of 10-2000 ng/mL(R^(2)>0.997).The limit of detection(LOD)and limit of quantification(LOQ)of synephrine and nmethyl tyramine were 0.3 ng/mL and 1 ng/mL,respectively.The recovery range was 94.3%-105.7%,and relative standard deviations(RSDs)were all less than 3%.This method avoids using phosphate and ion pair reagents,and only adding formic acid and ammonium formate in the mobile phase.The analytes have good retention and very high mass spectral response.Compared with the traditional method,this analytical method is fast,simple,specific,and it has a good application value in the separation and detection of large polar alkaloids.
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