Australian Centre for Research on Separation Science, School of Applied Sciences, R.M.I.T. University, GPO Box 2476, Melbourne, Victoria, 3001, Australia.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Jul 1;878(21):1761-70. doi: 10.1016/j.jchromb.2010.04.036. Epub 2010 May 20.
Metabolomics has been defined as the quantitative measurement of all low molecular weight metabolites (sugars, amino acids, organic acids, fatty acids and others) in an organism's cells at a specified time under specific environmental/biological conditions. Currently, there is considerable interest in developing a single method of derivatization and separation that satisfies the needs for metabolite analysis while recognizing the many chemical classes that constitute the metabolome. Chemical derivatization considerably increases the sensitivity and specificity of gas chromatography-mass spectrometry for compounds that are polar and have derivatizable groups. Microwave-assisted derivatization (MAD) of a set of standards spanning a wide range of metabolites of interest demonstrates the potential of MAD for metabolic profiling. A final protocol of 150 W power for 90 s was selected as the derivatization condition, based upon the study of each chemical class. A study of the generation of partially derivatized components established the conditions where this could potentially be a problem; the use of greater volumes of reagent ensured this would not arise. All compounds analyzed by comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry in a standard mixture showed good area ratio reproducibility against a naphthalene internal standard (RSD<10% in all but one case). Concentrations tested ranged from 1 microg/mL to 1000 microg/mL, and the calibration curves for the standard mixtures were satisfactory with regression coefficients generally better than 0.998. The application to gas chromatography-quadrupole mass spectrometry and comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry for a typical reference standard of relevance to metabolomics is demonstrated.
代谢组学被定义为在特定环境/生物条件下,在特定时间内定量测量生物体细胞中所有低分子量代谢物(糖、氨基酸、有机酸、脂肪酸等)。目前,人们对开发一种单一的衍生化和分离方法非常感兴趣,这种方法既能满足代谢物分析的需要,又能认识到构成代谢组的许多化学类别。化学衍生化大大提高了气相色谱-质谱法对具有衍生化基团的极性化合物的灵敏度和特异性。一组跨越广泛感兴趣的代谢物范围的标准品的微波辅助衍生化(MAD)表明 MAD 对代谢物图谱分析具有潜力。根据对每个化学类别的研究,选择 150 W 功率 90 s 的最终衍生化条件。对部分衍生化成分的生成的研究确定了可能出现这种情况的条件;使用更大体积的试剂可以确保不会出现这种情况。在标准混合物中通过全二维气相色谱-飞行时间质谱法分析的所有化合物均显示出与萘内标物良好的面积比重现性(除一种情况外,所有情况的 RSD<10%)。测试的浓度范围从 1μg/mL 到 1000μg/mL,标准混合物的校准曲线令人满意,回归系数通常大于 0.998。本文还展示了该方法在气相色谱-四极杆质谱法和全二维气相色谱-飞行时间质谱法中的应用,用于典型的与代谢组学相关的参考标准品。