Suppr超能文献

直接进样液相色谱/电喷雾电离质谱法对马尿进行分析以定量和确证用于兴奋剂检测的阈值物质。II. 可可碱的测定。

Direct injection liquid chromatography/electrospray ionization mass spectrometric horse urine analysis for the quantification and confirmation of threshold substances for doping control. II. Determination of theobromine.

作者信息

Vonaparti A, Lyris E, Panderi I, Koupparis M, Georgakopoulos C

机构信息

Doping Control Laboratory of Athens, Olympic Athletic Center of Athens 'Spiros Louis', 37 Kifissias Ave., 151 23 Maroussi, Greece.

出版信息

Rapid Commun Mass Spectrom. 2009 Apr;23(7):1020-8. doi: 10.1002/rcm.3967.

Abstract

In equine sport, theobromine is prohibited with a threshold level of 2 microg mL(-1) in urine, hence doping control laboratories have to establish quantitative and qualitative methods for its determination. Two simple liquid chromatography/mass spectrometry (LC/MS) methods for the identification and quantification of theobromine were developed and validated using the same sample preparation procedure but different mass spectrometric systems: ion trap mass spectrometry (ITMS) and time-of-flight mass spectrometry (TOFMS). Particle-free diluted urine samples were directly injected into the LC/MS systems, avoiding the time-consuming extraction step. 3-Propylxanthine was used as the internal standard. The tested linear range was 0.75-15 microg mL(-1). Matrix effects were evaluated analyzing calibration curves in water and different fortified horse urine samples. A great variation in the signal of theobromine and the internal standard was observed in different matrices. To overcome matrix effects, a standard additions calibration method was applied. The relative standard deviations of intra- and inter-day analysis were lower than 8.6 and 7.2%, respectively, for the LC/ITMS method and lower than 5.7 and 5.8%, respectively, for the LC/TOFMS method. The bias was less than 8.7% for both methods. The methods were applied to two case samples, demonstrating simplicity, accuracy and selectivity.

摘要

在马术运动中,可可碱是被禁止的,尿液中的阈值水平为2微克/毫升(-1),因此兴奋剂检测实验室必须建立其测定的定量和定性方法。开发并验证了两种简单的液相色谱/质谱(LC/MS)方法用于可可碱的鉴定和定量,使用相同的样品制备程序,但不同的质谱系统:离子阱质谱(ITMS)和飞行时间质谱(TOFMS)。将无颗粒稀释尿液样品直接注入LC/MS系统,避免了耗时的提取步骤。3-丙基黄嘌呤用作内标。测试的线性范围为0.75-15微克/毫升(-1)。通过分析水和不同加标马尿样品中的校准曲线来评估基质效应。在不同基质中观察到可可碱和内标的信号有很大差异。为了克服基质效应,采用了标准加入校准方法。LC/ITMS方法的日内和日间分析相对标准偏差分别低于8.6%和7.2%,LC/TOFMS方法分别低于5.7%和5.8%。两种方法的偏差均小于8.7%。这些方法应用于两个案例样品,证明了其简单性、准确性和选择性。

相似文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验