Department of Food Science, Agro Food Park 48, Aarhus N 8200, Denmark; CiFOOD, Centre for Innovative Research, Aarhus University. Agro Food Park 48, 8200 Aarhus N, Denmark.
Department of Food Science, Agro Food Park 48, Aarhus N 8200, Denmark.
J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Sep 1;1181:122902. doi: 10.1016/j.jchromb.2021.122902. Epub 2021 Sep 4.
Thermal processes are widely used in small molecule chemical analysis and metabolomics for derivatization, vaporization, chromatography, and ionization, especially in gas chromatography mass spectrometry (GC/MS). An optimized derivatization protocol has been successfully applied using multiple isotope labelled analytical internal standards of selected deuterated and C selected compounds, covering a range of different groups of metabolites for non-automated GC metabolomics (off-line). Moreover, the study was also realized in a pooled urine sample, following metabolic profiling. A study of thermal degradation of metabolites due to GC inlet and oven programs (fast, slow) was performed, where the results indicated that both GC oven programs (fast and slow) negatively affected the thermal stability of the metabolites, while the fast-ramp GC program also suppressed MS signals. However, the use of multiple internal standards can overcome this drawback. The application of extended temperature ramp GC program presented identical behaviour on metabolite stability and better chromatographic separation combined with much lower signal suppression, compared to a short temperature ramp program. No effects were observed for organic acids, fatty acids, sugars and sugar alcohols, while significant differences were observed for amino acids. GC metabolomics is a strong tool that can facilitate analysis, but special attention is required for sampling handling and heating, before and during the GC analysis. The use and application of multiple multi-group internal standards is highly recommended.
热分析过程在小分子化学分析和代谢组学中得到了广泛的应用,包括衍生化、蒸发、色谱和离子化等,尤其是在气相色谱质谱联用技术(GC/MS)中。本研究采用了多种同位素标记的分析内标物,对选定的氘代和 C 标记化合物进行了优化衍生化,覆盖了不同代谢物组的范围,用于非自动化 GC 代谢组学(离线)。此外,本研究还在代谢物谱分析后的混合尿样中进行了研究。对 GC 进样口和炉温程序(快速、缓慢)导致的代谢物热降解进行了研究,结果表明,两种 GC 炉温程序(快速和缓慢)均会降低代谢物的热稳定性,而快速升温 GC 程序还会抑制 MS 信号。然而,使用多个内标物可以克服这一缺点。与短升温程序相比,扩展温度 ramp GC 程序在代谢物稳定性和更好的色谱分离方面表现出相同的行为,同时信号抑制程度更低。有机酸、脂肪酸、糖和糖醇没有观察到影响,而氨基酸则观察到显著差异。GC 代谢组学是一种强大的分析工具,但在 GC 分析之前和期间,需要特别注意采样处理和加热。强烈推荐使用多组多内标物。