人血浆中甲氨蝶呤的高效液相色谱法测定及其代谢物的质谱定性分析
投稿时间:2014-04-03  修订日期:2014-06-26  点此下载全文
引用本文:王漪璇,毋丹,曹军宁,钱隽.人血浆中甲氨蝶呤的高效液相色谱法测定及其代谢物的质谱定性分析[J].药学实践杂志,2015,33(2):143~146,158
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王漪璇 复旦大学附属肿瘤医院肿瘤内科, 复旦大学上海医学院肿瘤学系, 上海 200032  
毋丹 复旦大学附属肿瘤医院肿瘤内科, 复旦大学上海医学院肿瘤学系, 上海 200032  
曹军宁 复旦大学附属肿瘤医院肿瘤内科, 复旦大学上海医学院肿瘤学系, 上海 200032  
钱隽 复旦大学附属肿瘤医院肿瘤内科, 复旦大学上海医学院肿瘤学系, 上海 200032 junqian@fudan.edu.com 
中文摘要:目的 建立固相萃取-高效液相色谱法测定人血浆中的甲氨蝶呤浓度,用于临床治疗的监测,并通过质谱对甲氨蝶呤的人体代谢物进行定性分析。 方法 血浆样本经C18固相萃取小柱净化洗脱后直接进样,以Diamonsil C18分析柱(150 mm×4.6 mm, 5 m)分离,流动相为甲醇和0.5%乙酸溶液(含0.3%三乙胺),采用梯度洗脱;流速为1.0 ml/min;紫外检测波长为306 nm。通过质谱全扫描(QLMS)和多反应监测-信息关联采集-增强子离子扫描(MRM-IDA-EPI)获得甲氨蝶呤代谢物的质谱信息。 结果 甲氨蝶呤在0.05~100 μmol/L范围内线性关系良好(r=0.999 9),提取回收率>95%,准确度在97%~105%之间,日内与日间精密度(RSD)均<5%。分析甲氨蝶呤代谢物的质谱信息,推断该代谢物为7-羟基甲氨蝶呤。 结论 本方法灵敏度高、重现性好、操作简便,适用于甲氨蝶呤的血药浓度监测。
中文关键词:甲氨蝶呤  高效液相色谱法  固相萃取  代谢物
 
Determination of methotrexate in human plasma by HPLC and qualitative analysis of its metabolite by mass spectrometry
Abstract:Objective To develop an SPE-HPLC method for the determination of methotrexate (MTX) in human plasma to monitor the clinical drug use of MTX, and to identify the human metabolite of MTX by mass spectrometry. Methods MTX was extracted from human plasma using C18 SPE column and analyzed directly after elution. The separation of MTX was performed on Diamonsil C18 column (150 mm×4.6 mm, 5 m) with a gradient mobile phase of methanol and 0.5% acetic acid solution (containing 0.3% triethylamine) at a flow rate of 1.0 ml/min. The detection wavelength was 306 nm. QLMS and MRM-IDA-EPI scan modes were used to obtain the mass spectrum of MTX metabolite. Results The calibration curve of MTX in plasma was linear over the range of 0.05-100 μmol/L(r=0.999 9). The extraction recovery was above 95% and accuracy was between 97% and 105%. Both intra-and inter-day precision were less than 5%. 7-OH MTX was identified to be the metabolite through the analysis of the mass spectrum. Conclusion The method is sensitive, reproducible, easy to operate and suits for monitoring the concentration of MTX in clinical practice.
keywords:methotrexate  HPLC  solid phase extraction  metabolite
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