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作 者:刘艳文[1,2] 张文渊[1,2] 颜苗[1,2] 李焕德[1] 朱荣华[1] 许丹华[1,2]
机构地区:[1]中南大学湘雅二医院临床药学教研室,长沙410011 [2]中南大学药学院,长沙410013
出 处:《中南药学》2010年第5期321-325,共5页Central South Pharmacy
基 金:湖南省中医药科研计划项目课题(No.2008086)
摘 要:目的建立小鼠血浆及脑组织中马钱子碱浓度的UPLC-MS/MS测定方法 ,用于小鼠马钱子碱药动学研究。方法色谱柱为Acquity UPLC BEHC18柱(2.1mm×50mm,1.7μm)。流动相为水(含0.1%甲酸)-甲醇(75:25,v/v),流速0.25mL.min-1,柱温40℃。吗氯贝胺为内标,采用ESI+模式,多重反应选择离子检测,马钱子碱m/z395→324,吗氯贝胺m/z269→182。样品处理采用液液萃取。结果马钱子碱在小鼠血浆中线性范围为5.016~5016ng.mL-1,脑组织中线性范围为3.009~725.4ng.g-1,日内精密度(RSD)均<8.5%,日间精密度(RSD)均<11.2%,方法回收率范围血浆中为91.7%~112.9%,脑组织中为95.6%~107.2%。结论本方法简单、灵敏、准确,适用于小鼠体内马钱子碱浓度测定及药动力学研究。Objective To develop an ultra-performance liquid chromatography tandem mass spectrometry for the determination of brucine in mice plasma and brain.Methods Acquity UPLC BEH C18 column(2.1 mm×50 mm,1.7 μm) was used with methanol-0.1% formic acid(25:75,v/v)as the mobile phase at 0.25 mL·min-1.The column temperature was 40℃.UPLC-ESI+-MS/MS was performed in the multiple reaction monitoring (MRM) mode using target ions at m/z 395→324 (brucine)and m/z 269→182(IS).The samples were extracted from mice plasma and brain using liquid-liquid extraction.Results The calibration curve of brucine was linear over 5.016-5 016 ng·mL-1 in the plasma,3.009-725.4 ng·g-1 in the brain.The methodology recovery was 91.7%-112.9% and 95.6%-107.2% in the plasma and the brain respectively.Inter-day and intra-day RSDs were all less than 15%.Conclusion The method is simple,sensitive and accurate for the study of brucine in mice.
关 键 词:马钱子碱 超高效液相色谱-串联质谱
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