LC/MS |
Highly sensitive technique.
Analyzes polar compounds of different weights based on an ionization method.
No derivatization needed.
Suitable for heat-sensitive compounds.
Compatible with liquids and solids.
Requires minimal sample volumes.
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Destructive technique.
Costly equipment requiring expertise.
Subject to unwanted solvent matrix effects.
Prolonged analysis duration (15–40 min/sample).
Generates variable adducts based on compound nature.
Not suitable for gases.
|
[9,12,85] |
GC/MS |
Quantitative, reproducible, and sensitive technique.
Direct analysis of volatile compounds.
Effective for analyzing mixtures and small hydrophobic organic and certain inorganic compounds.
Compatible with gases and liquids.
Generally, it is more cost-effective than LC-MS due to its simpler detector.
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Destructive technique.
Inappropriate for non-volatile and heat-sensitive compounds.
Necessitates separation and derivatization, which can mask the results.
Long analysis time (20–40 min per sample).
|
[9,12,85,86] |
MALDI-TOF-MS |
|
|
[79] |
NMR |
Quantitative non-destructive technique.
No requirement for harsh sample treatment before or during analysis.
A sole internal reference is sufficient for precise quantification of all spectrum metabolites.
Facilitates bio-fluid and tissue analysis without separation or preparation.
Rapid analysis (2–3 min/sample).
Analyzes both liquids and solids.
Derivatization is not required.
Automation integrated.
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Limited sensitivity.
Costly equipment.
Signal overlap from the absence of prior separation.
Does not identify inorganic ions or salts.
Cannot detect non-protonated samples.
Needs large sample volumes (0.1–0.5 mL).
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[9,12] |