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作 者:董海燕[1] 董亚琳[1] 王雪[1] 杨华[1] 刘娟娟[1]
机构地区:[1]西安交通大学医学院第一附属医院,西安710061
出 处:《药物分析杂志》2010年第2期199-203,共5页Chinese Journal of Pharmaceutical Analysis
摘 要:目的:建立高效液相色谱法快速测定人血清中利奈唑胺浓度,并用于危重患者治疗药物监测。方法:色谱柱:Hypersil ODS柱;流动相:乙腈-水(23:77),调整pH至5.0;流速:1.0mL.min-1;紫外检测波长为254nm。应用已建立的方法对9例危重患者进行利奈唑胺治疗药物监测,并合理制定个体化给药方案。结果:利奈唑胺在0.31~20.00mg.L-1浓度范围内线性关系良好(r=0.9996),最低定量限为0.31mg.L-1,绝对回收率为47.2%,相对回收率为102.1%,日内、日间精密度的RSD分别<4%和<3.5%。另外,所监测9例危重患者中,有4例患者出现利奈唑胺谷浓度小于最低抑菌浓度的情况。结论:HPLC法简单、快速、准确、灵敏、重现性好,可用于临床利奈唑胺的浓度监测。Objective:To establish a method of determining serum linezolid in human by HPLC,and use the method for therapeutic drug monitoring in critically ill patients.Methods:Separation was carried out on a Hypersil ODS column,the mobile phase consisted of acetonitrile-water (23∶77),adjust the pH to 5.0 at the flow rate of 1.0 mL/min-1.UV detection wavelength was 254 nm.The method has been used for nine critically ill patients for therapeutic drug monitoring,and individual dosage regimen of linezolid.Results:A good linearity was demonstrated between 0.31-20.00 mg/L-1 (r=0.9996),the lowest limit of quantification of 0.31 mg/L-1.The absolute recovery was 47.2%,and the relative recovery was 102.1%.The intra-day and inter-day deviation was showed by RSD〈4%,〈3.5%,respectively.In addition,the monitoring of nine critically ill patients,there are four patients with linezolid trough concentrations less than the minimum inhibitory concentrations.Conclusion:The method is simple,rapid,accurate,sensitive,reproducible,and validated for determination of serum linezolid in clinical practice.
关 键 词:利奈唑胺 高效液相色谱法 血药浓度 治疗药物监测
分 类 号:R917[医药卫生—药物分析学]
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