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作 者:周志凌[1,2] 杨敏[2,3] 余细勇[1,2] 单志新[1,2] 林秋雄[1,2] 麦丽萍[1,2] 邓春玉[1,2] 张梦珍[1,2] 陈铁峰[1,2] 刘晓颖[1,2] 陈秀云[1,2] 林曙光[1,2]
机构地区:[1]广东省人民医院/广东省医科院医学研究中心,广州510080 [2]广东省心血管病研究所,广州510080 [3]广东省人民医院/广东省医科院药学部,广州510080
出 处:《中国药房》2012年第46期4350-4352,共3页China Pharmacy
基 金:广东省自然科学基金(9151064101000063);广东省医学科研基金立项课题(A2011004)
摘 要:目的:建立测定人尿液中依非巴特浓度的方法。方法:尿液样品经蛋白沉淀后,采用液-质联用法进样测定,以甲醇-0.008mol·L-1甲酸铵水溶液(含0.1%甲酸)(35∶65)为流动相,AgilentZorbaxEclipseXDB-C18为色谱柱进行分离;采用电喷雾电离源,以多反应监测(MRM)方式进行正离子检测,用于定量分析的离子对依非巴特为m/z832.6→m/z646.4,内标为m/z931.6→m/z745.6。结果:依非巴特尿药浓度在5.0~5000.0ng·mL-1范围内线性关系良好(r=0.9996),最低定量限(LLOQ)为5.0ng·mL-1;日内和日间RSD均<7%,方法回收率为99.4%~103.1%,绝对回收率≥93%。结论:本方法选择性强、灵敏度高、重现性好,能快速、准确测定人尿液中依非巴特的浓度,并且成功用于依非巴特尿药排泄的研究。OBJECTIVE: To establish the method for the determination of eptifibatide in human urine. METHODS: Following protein precipitation, LC-MS method was adopted. The determination was performed on a Agilent Zorbax Eclipse XDB-C18 (150 mm×4.6 mm,5 μm) column with mobile phase consisted of methanol-0.008 mol·L-1 ammonium formate (containing 0.1% formic acid)(35∶65). Electrospray ionization source was used as detector and operated in the positive ion mode. Quantification was performed using multiple reaction monitoring (MRM) of the transitions m/z of 832.6→646.4 and 931.6→745.6 for eptifibatide and internal standard, respectively. RESULTS: The linear range was 5.0~5 000.0 ng·mL-1 for eptifibatide (r=0.999 6) with the LLOQ of 5.0 ng·mL-1. The intra-day and inter-day RSDs were less than 7%. Method recoveries were 99.4%~103.1% and absolute recovery was no less than 93%. CONCLUSION: The method is selective, sensitive, reproducible, rapid and accurate for the determination of eptifibatide in human urine and study of eptifibatide excretion.
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