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引用本文:王盈盈,王陈翔,胡卢丰,周子晔,张秀华.HPLC测定人血浆中亚胺培南的浓度[J].中国现代应用药学,2013,30(12):1349-1352.
WANG Yingying,WANG Chenxiang,HU Lufeng,ZHOU Ziye,ZHANG Xiuhua.Determination of Imipenem in Human Plasma by HPLC[J].Chin J Mod Appl Pharm(中国现代应用药学),2013,30(12):1349-1352.
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HPLC测定人血浆中亚胺培南的浓度
王盈盈, 王陈翔, 胡卢丰, 周子晔, 张秀华
温州医科大学附属第一医院药学部,浙江 温州 325000
摘要:
目的 建立测定人血浆中亚胺培南浓度的HPLC方法。方法 以0.5 mol·L-1尿素为稳定剂,以5-溴脲嘧啶为内标,血浆样品经乙腈沉淀蛋白,二氯甲烷2次提取去杂质,取水相进样。色谱柱为Atlantis C18(4.6 mm×150 mm,5 μm);流动相为甲醇-10 mmol·L-1磷酸二氢钾溶液(pH=6.0)(4∶96);流速为1.0 mL·min-1;柱温:25 ℃;检测波长:300 nm。结果 亚胺培南在0.5~100 mg·L-1内线性关系良好,r=0.999 7;定量下限为0.5 mg·L-1;平均绝对回收率 82.72%,方法回收率为87.60%~96.36%;日内、日间RSD均<10%。结论 本方法简单、快捷、灵敏、准确,适用于亚胺培南临床血药浓度的监测。
关键词:  高效液相色谱法  亚胺培南  人血浆
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Determination of Imipenem in Human Plasma by HPLC
WANG Yingying, WANG Chenxiang, HU Lufeng, ZHOU Ziye, ZHANG Xiuhua
Department of Pharmary, the First Affiliated Hospital of Wenzhou Medical University, WenZhou 325000, China
Abstract:
OBJECTIVE To establish an HPLC method for the detection of imipenem in human plasma. METHODS Samples were spiked with 0.5 mol·L-1 urea as stabilizer solution, 5-bromine urea pyrimidine as internal standard, proteins were precipitated with acetonitrile followed by extraction with dichloromethane and the upper aquous phase was injected. Separation was achieved on an Atlantis C18 column (4.6 mm×150 mm, 5 μm). The mobile phase composed of methanol and 10 mmol·L-1 monopotassium phosphate (pH=6.0)(4∶96) with a flow rate of 1.0 mL·min-1. The column temperature was 25 ℃. The UV detection wavelength was 300 nm. RESULTS Calibration curves of imipenem showed good linear regression in the range of 0.5-100 mg·L-1(r=0.999 7). The lower limit of quantification of imipenem was 0.5 mg·L-1. The mean absolute recovery was 82.72%, and the method recovery was 87.60%-96.36%. Intra- and inter-day variations were <10%. CONCLUSION The established method is simple, sensitive and accurate for determining imipenem in human plasma.
Key words:  HPLC  imipenem  human plasma
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