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Methodological considerations in the development of HPLC-MS methods for the analysis of rodent plasma for metabonomic studies

机译:开发用于代谢组学研究的啮齿动物血浆的HPLC-MS方法的方法学考虑

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摘要

A study of the factors involved in obtaining valid global metabolite profiles from the HPLC-MS of rat or mouse plasma for the purposes of metabonomic analysis has been undertaken. Plasma proteins were precipitated with three volumes of either methanol or acetonitrile. Chromatographie separations were performed on a CIS-bonded stationary phase using 3.5 and 5 μm particles packed into 2.1 and 4.6 mm i.d. formats, respectively, and on a C8 phase using 3.5 μm particles and a 2.1 mm i.d. column. Three reversed-phase gradient solvent systems, based on acidified water-acetonitrile, acidified water-methanol and acidified water-methanol-acetonitrile mixtures, were investigated. The column eluent was analysed with both positive and negative clcctrospray ionisation using a quadrupole-linear ion trap mass spectrometer. These studies revealed that while accurate classification of sample type can be made, there are a number of methodological problems associated with the analysis of plasma with respect to factors such as repeatability and column longevity. In particular, special care has to be taken to ensure that the analytical system is properly "conditioned" by the repeated injection of matrix samples. The use of biological quality control (QC) samples provided an important means of monitoring method performance. Finally, the source of the plasma (Zucker wild-type or (fa/fa) rat or mouse tumour model) also appeared to have an effect on the repeatability of the methodology.
机译:为了进行代谢组学分析,已经对从大鼠或小鼠血浆的HPLC-MS获得有效的整体代谢物图谱的因素进行了研究。用三倍体积的甲醇或乙腈沉淀血浆蛋白。色谱分离是在CIS键合固定相上进行的,其中使用填充在2.1和4.6 mm内径中的3.5和5μm颗粒。在C8相上分别使用3.5μm颗粒和2.1 mm i.d.柱。研究了基于酸化水-乙腈,酸化水-甲醇和酸化水-甲醇-乙腈混合物的三种反相梯度溶剂体系。使用四极线性离子阱质谱仪同时对正离子和负离子进行喷雾电离分析柱洗脱液。这些研究表明,尽管可以对样品类型进行准确的分类,但是在血浆分析方面存在许多方法学问题,例如重复性和色谱柱寿命。特别是,必须格外小心,以确保通过重复注入基质样品适当地“调节”分析系统。生物质量控制(QC)样品的使用提供了监测方法性能的重要手段。最后,血浆来源(Zucker野生型或(fa / fa)大鼠或小鼠肿瘤模型)似乎也对方法的可重复性产生影响。

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  • 来源
    《Molecular BioSystems》 |2010年第1期|108-120|共13页
  • 作者单位

    Dept of Drug Metabolism and Pharmacokinetics, AstraZeneca, Mereside, Alderley Park, Macclesfield, Cheshire, UK SK10 4TG;

    rnDept of Drug Metabolism and Pharmacokinetics, AstraZeneca, Mereside, Alderley Park, Macclesfield, Cheshire, UK SK10 4TG Laboratory of Analytical Chemistry, Aristotle University of Thessaloniki, 541 24, Greece;

    rnLaboratory of Analytical Chemistry, Aristotle University of Thessaloniki, 541 24, Greece;

    rnLaboratory of Analytical Chemistry, Aristotle University of Thessaloniki, 541 24, Greece;

    rnAstraZeneca, Mereside, Alderley Park, Macclesfield, Cheshire, UK SK10 4TG;

    rnAstraZeneca, Mereside, Alderley Park, Macclesfield, Cheshire, UK SK10 4TG;

    rnApplied Biosvstems/MDS Analytical Technologies, Concord, ON, Canada L4K 4V8;

    Applied Biosvstems/MDS Analytical Technologies, Concord, ON, Canada L4K 4V8;

    rnApplied Biosvstems/MDS Analytical Technologies, Concord, ON, Canada L4K 4V8;

    rnDept of Drug Metabolism and Pharmacokinetics, AstraZeneca, Mereside, Alderley Park, Macclesfield, Cheshire, UK SK10 4TG;

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