Table 1.
Technique | Major Strengths | Major Limitations | Major Detectable Compounds |
---|---|---|---|
GC-MS | Efficient and reproducible chromatography separation Comprehensive mass spectral libraries |
Labor-intensive, time-consuming and varying sample preparation procedure Complicated identification of unknown compounds |
Volatile and thermo-stable compound Carbohydrates Esters Sterols Steroids Eicosanoids Fatty acids Aminoacids Organic acids Nucleotides and nucleosides Lipids Non-volatile and thermo-labile compounds |
LC-MS | Broad range of compounds (including polar, bulky, and thermo-labile metabolites) can be analyzed without derivatization High throughput |
Possibility of ion aberrations resulting from a sample matrix Lack of spectral libraries for identification of metabolites |
|
NMR | Non-destructive analysis High reproducibility Simple or even absent sample preparation |
Low sensitivity Relatively high sample volume High cost of apparatus |
Carbohydrates Amines Aminoacids and organic acids Bulky molecules |