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作 者:饶志[1] 秦红岩[1] 邵云云[1,2] 黄静[1,2] 武新安[1]
机构地区:[1]兰州大学第一医院药剂科,兰州730000 [2]兰州大学药学院,兰州730000
出 处:《中国药学杂志》2014年第14期1252-1257,共6页Chinese Pharmaceutical Journal
摘 要:目的建立应用LC-MS/MS进行大鼠血浆、尿液、结肠中美沙拉嗪及其体内代谢物N-乙酰-5-ASA浓度的测定方法,并将其应用于美沙拉嗪及N-乙酰-5-ASA在大鼠体内过程的研究。方法血浆、尿液及结肠样品均用甲醇沉淀蛋白进行提取,以ESI电离源在负离子模式下检测,用Agilent HC-C18色谱柱,甲醇-醋酸水溶液为流动相梯度洗脱,流速为1.0 mL·min-1。结果美沙拉嗪及N-乙酰-5-ASA在大鼠血浆、尿液及结肠中的线性范围及定量限均符合测定要求,日内、日间精密度及基质效应均<15%。结论本方法快速、灵敏、专属性强且重现性好,可用于大鼠血浆、尿液、结肠中美沙拉嗪及N-乙酰-5-ASA测定。OBJECTIVE To develop an LC-MS/MS method for determination of mesalazine and its metabolite, N-Ac-5-ASA, in rat plasma, urine and colon for the pharmaeokinetic study of mesalazine and N-Ac-5-ASA in rats. METHODS The plasma, urine and colon samples were treated with methanol to precipitate protein. An Agilent HC-CI8 column was used as the analytical column, with methanol and acetic acid aqueous solution as mobile phase eluted by a gradient program at a flow rate of 1.0 mL · min-1. The detection was accomplished with ESI source operated in negative ionization mode. RESULTS The linearity and LLOQs of mesalazine and N-Ac-5-ASA in rat plasma, urine and colon both met the requirements, and the inter- and intra-day RSDs and matrix effect were less than 15%. CONCLUSION This assay is a rapid, sensitive, selective and reliable method for determination of mesalazine and N-Ac- 5-ASA in rat plasma, urine and colon.
关 键 词:高效液相色谱-质谱联用 美沙拉嗪 N-乙酰-5-ASA
分 类 号:R917[医药卫生—药物分析学]
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