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. 2022 Oct 5;38(12):1457–1487. doi: 10.1007/s44211-022-00190-8

Table 2.

Various retention modes and typical steps that carried out during the SPE process

Sorbent phase type Bed sorbent Structure of bonded phases Bonded function Target analyte Solvents
Conditioning Rinse Elution
Normal-phase Amino (-NH2) -(CH2)NH2

Polar interactions

Hydrogen bonding Dipolar attraction

Exhibits polar functionalities (hydroxyl, carbonyls, amines, double bonds, compounds with heteroatoms) Nonpolar solvent (hexane, chloroform) Nonpolar solvent Strong polar eluent (such as methanol)
Diol (C–OH C–OH) Spaced-bonded propanediol
Cyano (-CN) -(CH2)3CN

Polar interactions

Adsorption

Silica gel -SiOH
Florisil Mg2SiO3
Alumina Al2O3
Reversed-phase Triacontyl -C30H61

Adsorption/hydrophobic interaction

van der Waals forces

Slightly non-polar

Moderately non-polar

Nonpolar

MeOH/H2O

ACN/H2O

with appropriate pH

Polar solvent

With appropriate pH

Strong non-polar (hexane, chloroform)

Polar to semi-polar (methanol)

Octadecyl (C18) -(CH2)17CH3
Octyl (C8) -(CH2)7CH3
Ethyl (C2) -CH2CH3
Cyclohexyl CH2-Cyclohexyl
Phenyl CH2-Phenyl
Ion exchange SCX Sulfonic Propanesulfonic acid Electrostatic attraction (cation exchange-ionic base) Positive charge analytes

Water or buffer

pH > 7

(pH = pKa − 2)

pH = pKa-2 Eluent with ionic strength (pH = pKa + 2)
Benzenesulfonic acid
WCX Carboxylic acid Carboxylpropyl
SAX Quaternary ammonium Trimethylaminopropyl Electrostatic attraction (anion exchange-ionic acid) Negative charge analytes

Water or buffer

pH < 7

pH = pKa + 2

pH = pKa + 2 Eluent with high ionic strength (pH = pKa-2)
WAX Primary, secondary, or tertiary amines