Table 1.
Metabolomic Technology |
Advantage | Disadvantage |
---|---|---|
GC-MS | High sensitivity; Easy to operate; Economical; Search the unknown material spectrum library; Suitable for volatile and non–thermosenitive compounds. | The compound may change; Not suitable for less volatile compounds. |
LC-MS | Suitable for metabolites with low volatility; Poor thermal stability and mixture analysis; High sensitivity; Wide range; Fast; Qualitative and quantitative analysis. | Poor ability to distinguish isomers and stereochemistry; Poor reproducibility; Strict operating conditions; Memory effects and ion sources contamination; Complex and expensive operation; Quality discrimination effect. |
ES-MS | No special treatment for samples; Low dosage; Economical; Fast; High sensitivity; High-throughput; Short test time; Multiple modes. | Poor preparation ability; Low sensitivity in some detection methods; Low separation reproducibility. |
MSI | No fluorescence or radioisotope labeling; Wide mass range; High-throughput; High efficiency; Spatial resolution; Molecular specificity. | New matrix development and its application is demanded in MALDI-MSI. |
NMR | Non-destructive sample; Quantified directly; High NMR signal intensity isotopic natural abundance show extraordinarily narrow line widths; Broad (~200 ppm) chemical shift rane. | Magnetic nuclei only; Low sensitivity; A greater likelihood of overlapping peaks; Low sensitivity. |