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机构地区:[1]上海中医药大学附属曙光医院,上海200021
出 处:《中国医院药学杂志》2015年第19期1719-1723,共5页Chinese Journal of Hospital Pharmacy
基 金:国家十一五重大新药创制专项(编号:2010ZX09102-208);2013年国家临床重点专科(中医专业)临床药学建设项目(编号:财社[2013]239号)
摘 要:目的:建立液相色谱一串联质谱(LC-MS/MS)法,同时测定复方鹿角颗粒水解后18种氨基酸的含量。方法:样品经过150℃水解1h处理后直接进样,无需进行衍生化和固相萃取等烦琐的前处理步骤。液相色谱柱为Agilent Zorbax Eclipse AAA(4.6rm×150mm,5μm)。采用0.1%甲酸水溶液和90%乙腈水溶液为流动相进行梯度洗脱;洗针液为50%乙腈水溶液(含0.1%甲酸),流速为0.2ml·min。结果:18种氨基酸的检出限(LOD)为3.00-30.0ng·ml-1,线性相关系数均大于0.9978,峰面积测定的相对标准偏差(RSD)在5%以内。结论:该方法分析效率高、灵敏度和选择性高,适用于复方鹿角颗粒氨基酸的定性定量分析。OBJECTIVE To determine contents of amino acids in compound Lujiao granules by liquid chromatography tandem mass spectrometry (LC-MS/MS). METHODS Compound Lujiao granules were hydrolyzed for 1 hour at 150 ℃ and analyzed directly without derivatization or solid phase extraction. LC separation was carried on a Agilent Zorbax Eclipse AAA (4. 6 ram x 150 ram, 5/μm) column with mobile phase of water solution containing 0. 1 % formic acid and acetonitrile/water (v/v, 90 :10) at flow rate of 0. 2 ml. min-1 in gradient mode. RESULTS Limits of detection (LOD) of eighteen amino acids were in range of 3.00-30. 0 ng. ml-1 (S/N = 3), linear correlation coefficients were above 0. 9978 in all cases. Relative standard devia- tions (RSDs) of peak areas of extracted ion chromatograms were in range of 5%. CONCLUSION LC-MS/MS is efficient, sensitive and selective, which is helpful for determination of amino acids incompound Lujiao granules.
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