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作 者:殷望[1,2] 王瑜[1,2] 杨俊[2] 康仪[2] 刘进[2] 张文胜[2]
机构地区:[1]四川大学华西药学院,四川成都610041 [2]四川大学华西医院麻醉与危重急救研究室,四川成都610041
出 处:《华西药学杂志》2012年第1期80-83,共4页West China Journal of Pharmaceutical Sciences
摘 要:目的采用高效液物色谱一串联质谱(HPLC-MS/MS)测定家兔全血中水溶性异丙酚前药磷丙泊酚钠的浓度。方法采用Welch Ultimate XB C8柱(100 mm×2.1 mm,3μm),7-羟基香豆素为内标,流动相为5 mmol.L-1乙酸铵-乙腈(57∶43),流速0.4 mL.min-1。HPLC-MS/MS采用负离子电喷雾离子源,以多反应离子模式监测。全血样品经含内标的甲醇溶液直接沉淀蛋白后进样。结果标准曲线的线性范围是0.12~15μg.mL-1,最低定量下限为120 ng.mL-1;日内和日间RSD小于7.04%,RSD均小于8.40%。结论所用方法简便快速、准确灵敏,可用于磷丙泊酚钠血药浓度的测定和药动学的研究。OBJECTIVE To develope a liquid chromatography-tandem mass spectrometry(HPLC-MS/MS)method for the determination of fospropofol in the rabbit whole blood.METHODS The analysis was conducted using a Welch Ultimate C18 column(100 mm×2.1 mm,3 μm).7-hydroxycoumarin was used as internal standard.The mobile phase consisted of ammonium acetate(5 mmol·L-1) and acetonitrile(57∶43) at a flow rate of 0.4 mL·min-1.Negative electrospay ionization(ESI-) was used for LC-MS/MS determination.Quantification was performed in multiple reaction monitoring(MRM) mode.Blood samples were prepared by protein precipitation with methanol containing internal standard.RESULTS Calibration curves were established over a range of 0.12-15 μg·mL-1 with a lower quantification limit of 120 ng·mL-1.The intra-and inter-day accuracy expressed as relative error(RE) were within 7.04% and RSD were below 8.40%.CONCLUSION The method is simple,rapid,accurate,sensitive and could be used for the determination of fospropofol in blood samples and for its pharmacokinetic studies.
分 类 号:R917[医药卫生—药物分析学]
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