Solid phase extraction is routinely selected as a sample preparation technique prior to HPLC and GC analysis. It provides:
This works well for any homogeneous liquid samples, but clearly a solid sample cannot be applied directly to an SPE device. Here, we will consider how best to approach the handling of solid samples prior to SPE.
The first stage of sample pre-treatment involves homogenising the solid sample with a suitable solvent. The solvent selected for this purpose will:
Having formed a suspension of the sample in a suitable solvent the sample should be vortexed to promote thorough mixing, and then centrifuged to pellet the insoluble components of the matrix. The solvent should then be removed for further treatment.
At this point the SPE mechanism needs to be selected:
Mechanism | Weak Solvent | Strong Solvent |
---|---|---|
Reversed Phase | Water/buffer | Acetonitrile/Methanol (hexane strongest) |
Normal Phase | Hexane/Heptane | Mid polar organic such as DCM, MTBE, IPA (strongest is water) |
Ion Exchange | Aqueous buffer at a pH which promotes ion exchange interactions between analyte and SPE sorbent | Organic solvent, typically methanol with pH adjustment to disrupt the ion exchange interactions. |
Analyte properties and sample diluent both need to be considered at this point. Reversed phase extractions are effective for moderately polar to moderately hydrophobic analytes, but only if they are dissolved in a weak solvent such as water. If the sample is dissolved in a mid-polar solvent the sample will either need to be diluted, or alternatively dried down and reconstituted. The same is true for normal phase, where samples need to be dissolved in hexane/heptane for analytes to be successfully retained during sample loading onto the SPE device.
These examples will hopefully illustrate this concept:
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