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Choosing the best SPE stationary phase to use depends on the physical/chemical properties (such as pH, pKa and Solubility log P) of your analytes. There are a variety of SPE stationary phases to choose from including: reverse phase, normal phase, ion-exchange, and mixed mode, with mixed mode being a mixture of both normal and reversed phases. This page helps you decide which phase to use when.
Table 1 shows the basic mechanism of separation for each of these phases, while Figure 1 shows that phase selection starts with determining if your sample is soluble in water or organic solvent, your analyte’s characteristics, and which SPE stationary phase to use for each. Figure 1 also shows typical SPE stationary phases used for different applications. Figure 1 is an SPE Phase Selection Flow Chart that shows which Thermo Scientific SPE phase to use depending on your analytes’ solubility and charge.
Table 1: Mechanisms of SPE phase separation | |||
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Reverse Phase | Normal Phase | Ion Exchange | |
Retention Mechanism |
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Analyte Characteristics |
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Sample Matrices |
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Elution Considerations | Disrupt interaction with solvents with adequate non-polar character | Disrupt interaction with solvents with a more polar character | Disrupt interactions by:
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Common Sorbents |
| Bare silica, Alumina, Bonded silica (aminopropyl, diol) Florisil | Bonded silica (SAX, WAX; SCX, WAX) |
Figure 1. shows the phase (sorbent) depending on if your sample is soluble in a polar, moderately polar, or non-polar organic solvent polar or if your sample is soluble in water soluble if it is ionic or non-ionic.
Polymerics | Reversed Phase Silica Phases | Normal Phase Silica Phases | Ion Exchange Phases |
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SPE Phase | Functionality | Surface area | Particle size | Pore size | Analyte | Typical Applications |
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SOLA & SOLAµ HRP | Polystyrene divinylbenzene material surface functionalized with pyrolidone | 700 to 900m2/g | 19 to 25µm | 30 to 110Å | Retention of polar and non-polar analytes |
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HyperSep Retain PEP Polystyrene | Divinylbenzene material surface modified with urea groups | 550 – 750m2 /g | 40 – 60μm | 55 – 90Å | Retention of polar and non-polar analytes |
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Separates using non-polar interactions: Van der Waals or dispersion force
SPE Phase | Functionality | Surface area | Particle size | Pore size | Analyte | Typical Applications |
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HyperSep C18 | Highly retentive alkyl-bonded silica phase | 470 – 530m2 /g | 40 – 60μm | 60Å | Retains non-polar to moderately polar compounds |
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HyperSep C8 | Less retentive alternative to C18 | 470 – 530m2 /g | 40 – 60μm | 60Å | Retains non-polar to moderately polar compounds | |
HyperSep Phenyl | silica-based material with alternative selectivity for basic compounds | 470 – 530m2 /g | 40 – 60μm | 60Å | aromatic compounds with a benzene ring in its structure |
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These comprise of two functional groups: either non-polar and ion exchange, or hydrophobic and ionic retention. They are ideal for samples with complex structures.
SPE Phase | Functionality | Surface area | Particle size | Pore size | Analyte | Typical Applications |
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SOLA & SOLAµ SCX (mixed mode) | Next generation Polystyrene divinylbenzene material surface functionalized with sulphonate groups | 550 – 750m2 /g | 19 to 25µm | 30 to 110Å | a versatile polymeric material for the enhanced retention of weak bases |
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SOLA & SOLAµ SAX (mixed mode) | Next generation Polystyrene divinylbenzene material surface functionalized with quaternary groups | 550 – 750m2 /g | 40 – 60μm | 55 – 90Å | Polymeric material for the retention of weak acids |
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SOLA & SOLAµ WCX (mixed mode) | Next generation Polystyrene divinylbenzene material surface functionalized with carboxcylic acid groups | 550 – 750m2 /g | 19 to 25µm | 30 to 110Å | a versatile polymeric material for the enhanced retention of strong bases |
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SOLA & SOLAµ WAX (mixed mode) | Next generation Polystyrene divinylbenzene material surface functionalized with tertiary amine groups | 550 – 750m2 /g | 19 to 25µm | 30 to 110Å | a versatile polymeric material for the enhanced retention of strong acids |
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HyperSep Retain-CX | Versatile polymeric material for retention of basic compounds | 550 – 750m2 /g | 40 – 60μm | 55 to 90Å | a versatile polymeric material for the enhanced retention of basic compounds | a wide range of drugs of abuse from biological matrices |
HyperSep Retain-AX | Versatile polymeric material for retention of acidic compounds | 550 – 750m2 /g | 40 – 60μm | 55 – 90Å | a versatile polymeric material for the enhanced retention of acidic compounds | acidic drugs of abuse from biological matrices, such as THC and its metabolites |
HyperSep Hypercarb | Unique material for retention of highly polar compounds |
| Retention of extremely polar compounds | Ideal for problem analytes |
SPE Phase | Functionality | Surface area | Particle size | Pore size | Analyte | Typical Applications |
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HyperSep Silica | A polar sorbent primarily used to retain analytes from non-polar matrices | 530m2 /g | 40 – 60μm | 60Å | extract analytes from non-polar solvents such as hydrocarbon, less polar esters and ethers |
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HyperSep Florisil | magnesia-loaded silica gel | 289m2 /g | 40 – 60μm | 60Å | isolation of polar compounds from non-polar matrices |
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HyperSep Cyano | silica-based material of low hydrophobicity that is retentive than either silica or diol. | 470 – 530m2 /g | 40 – 60μm | 60Å | Retention of polar compounds from non-polar matrices |
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HyperSep Diol | silica-based material for extraction of polar compounds | 470 – 530m2 /g | 40 – 60μm | 60Å | of polar compounds | normal phase extraction and purification of polar compounds |
HyperSep Aminopropyl | silica-based material used as both a polar sorbent and a weak anion exchanger | 470 – 530m2 /g | 40 – 60μm | 60Å | petroleum fractionation, saccharides, drugs and drug metabolites |
SPE Phase | Functionality | Surface area | Particle size | Pore size | Analyte | Typical Applications |
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HyperSep SAX (Strong Anion Exchanger) | Strong anion exchange sorbent for extraction of weak acids | 470-530m2 /g | 40 – 60μm | 60Å |
| removal of
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HyperSep SCX (Strong Cation Exchanger) | Strong cation exchange sorbent for extraction of charged basic compounds | 470-530m2 /g | 40 – 60μm | 60Å | extraction of positively charged compounds from both aqueous and non-aqueous matrices | Extraction of antibiotics, drugs, organic bases, amino acids, catecholamines and herbicides |
SPE Phase | Functionality | Surface area | Particle size | Pore size | Analyte | Typical Applications |
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HyperSep Verify-CX | Reversed phase C8 group and a strong cation exchanger | 470-530m2 /g | 40 – 60μm | 60Å | Non-polar and anionic characteristics for improved analysis of basic drugs of abuse | Range of basic drugs of abuse from biological matrices |
HyperSep Verify-AX | a reversed phase C8 group and a strong anion exchanger | 470-530m2 /g | 40 – 60μm | 60Å | analysis of acidic drugs of abuse | A range of acidic drugs of abuse from biological matrices including THC and its metabolites |
The stationary phase, differing in particle size and distribution, can be packed in a cartridge, 96-well plates, and even pipette tips.
Table 3. Typical sorbent mass, sample size, and elution volumes used for different SPE cartridge sizes
Cartridge Volume | Sorbent Mass | Sample Size | Minimum Elution Volume |
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1mL | 50-100mg | 2.5-10mg | 100-200mL |
3mL | 500mg | 25-100mg | 1-3mL |
6mL | 500-1000mg | 25-100mg | 2-6mL |
12mL | 2000mg | 100-200mg | 10-12mL |
The choice of solvent is dependent upon the sample matrix and the retention mechanism used. The table below shows the differing polarities of solvents commonly used in SPE.
The choice of solvent to extract the analyte is dependent on the analyte properties.