Chemistry:Solid phase extraction
Solid-phase extraction (SPE) is an extractive technique by which compounds that are dissolved or suspended in a liquid mixture are separated from other compounds in the mixture according to their physical and chemical properties. Analytical laboratories use solid phase extraction to concentrate and purify samples for analysis. Solid phase extraction can be used to isolate analytes of interest from a wide variety of matrices, including urine, blood, water, beverages, soil, and animal tissue.[1][2][3]
SPE uses the affinity of solutes dissolved or suspended in a liquid (known as the mobile phase) for a solid through which the sample is passed (known as the stationary phase) to separate a mixture into desired and undesired components. The result is that either the desired analytes of interest or undesired impurities in the sample are retained on the stationary phase. The portion that passes through the stationary phase is collected or discarded, depending on whether it contains the desired analytes or undesired impurities. If the portion retained on the stationary phase includes the desired analytes, they can then be removed from the stationary phase for collection in an additional step, in which the stationary phase is rinsed with an appropriate eluent.
Many of the adsorbents/materials are the same as in chromatographic methods, but SPE is distinctive, with aims separate from chromatography, and so has a unique niche in modern chemical science.
SPE and chromatography
SPE is not a method of chromatography, except in the broadest, simplest sense. It is an extractive technique, a solid-liquid extractive technique—taking advantage of large differences in the Keq, or equilibrium constant, of mixture components between the solid phase and the mobile phase resulting, for a well-designed and executed separation, in a bulk separation of one or more of the mixture components so that it is significantly enriched as a result of the rapid extractive procedure. Granted many of the adsorbents/materials are the same as in chromatographic methods, and when these materials are packed into long columns—such that the number of theoretical plates increases by orders of magnitude as a result—the same materials result in chromatographic separations of components with even small difference is their Keq between phases. Even so, grey line that it might be that divides SPE and chrom, the distinctives are clear enough to say that SPE is an extractive technique, with theory, procedures, and aims separate from chromatography, and so with a unique niche in modern chemical science.
Normal phase SPE procedure
A typical solid phase extraction involves five basic steps. First, the cartridge is equilibrated with a non-polar or slightly polar solvent, which wets the surface and penetrates the bonded phase. Then water, or buffer of the same composition as the sample, is typically washed through the column to wet the silica surface. The sample is then added to the cartridge. As the sample passes through the stationary phase, the polar analytes in the sample will interact and retain on the polar sorbent while the solvent, and other non-polar impurities pass through the cartridge. After the sample is loaded, the cartridge is washed with a non-polar solvent to remove further impurities. Then, the analyte is eluted with a polar solvent or a buffer of the appropriate pH.
A stationary phase of polar functionally bonded silicas with short carbons chains frequently makes up the solid phase. This stationary phase will adsorb polar molecules which can be collected with a more polar solvent.[3]
Reversed phase SPE
Reversed phase SPE separates analytes based on their polarity. The stationary phase of a reversed phase SPE cartridge is derivatized with hydrocarbon chains, which retain compounds of mid to low polarity due to the hydrophobic effect. The analyte can be eluted by washing the cartridge with a non-polar solvent, which disrupts the interaction of the analyte and the stationary phase.[3]
A stationary phase of silicon with carbon chains is commonly used. Relying on mainly non-polar, hydrophobic interactions, only non-polar or very weakly polar compounds will adsorb to the surface.[3]
Ion exchange SPE
Ion exchange sorbents separate analytes based on electrostatic interactions between the analyte of interest and the positively or negatively charged groups on the stationary phase. For ion exchange to occur, both the stationary phase and sample must be at a pH where both are charged.
Anion exchange
Anion exchange sorbents are derivatized with positively charged functional groups that interact and retain negatively charged anions, such as acids. Strong anion exchange sorbents contain quaternary ammonium groups that have a permanent positive charge in aqueous solutions, and weak anion exchange sorbents use amine groups which are charged when the pH is below about 9. Strong anion exchange sorbents are useful because any strongly acidic impurities in the sample will bind to the sorbent and usually will not be eluted with the analyte of interest; to recover a strong acid a weak anion exchange cartridge should be used. To elute the analyte from either the strong or weak sorbent, the stationary phase is washed with a solvent that neutralizes the charge of either the analyte, the stationary phase, or both. Once the charge is neutralized, the electrostatic interaction between the analyte and the stationary phase no longer exists and the analyte will elute from the cartridge.[3]
Cation exchange
Cation exchange sorbents are derivatized with functional groups that interact and retain positively charged cations, such as bases. Strong cation exchange sorbents contain aliphatic sulfonic acid groups that are always negatively charged in aqueous solution, and weak cation exchange sorbents contain aliphatic carboxylic acids, which are charged when the pH is above about 5. Strong cation exchange sorbents are useful because any strongly basic impurities in the sample will bind to the sorbent and usually will not be eluted with the analyte of interest; to recover a strong base a weak cation exchange cartridge should be used. To elute the analyte from either the strong or weak sorbent, the stationary phase is washed with a solvent that neutralizes ionic interaction between the analyte and the stationary phase.[3]
Cartridges
The stationary phase comes in the form of a packed syringe-shaped cartridge, a 96 well plate, a 47- or 90-mm flat disk, or a microextraction by packed sorbent (MEPS) device, a SPE method that uses a packed sorbent material in a liquid handling syringe.[4][5] These can be mounted on its specific type of extraction manifold. The manifold allows multiple samples to be processed by holding several SPE media in place and allowing for an equal number of samples to pass through them simultaneously. In a standard cartridge SPE manifold up to 24 cartridges can be mounted in parallel, while a typical disk SPE manifold can accommodate 6 disks. Most SPE manifolds are equipped with a vacuum port, where vacuum can be applied to speed up the extraction process by pulling the liquid sample through the stationary phase. The analytes are collected in sample tubes inside or below the manifold after they pass through the stationary phase.
Solid phase extraction cartridges and disks are available with a variety of stationary phases, each of which can separate analytes according to different chemical properties. Most stationary phases are based on silica that has been bonded to a specific functional group. Some of these functional groups include hydrocarbon chains of variable length (for reversed phase SPE), quaternary ammonium or amino groups (for anion exchange), and sulfonic acid or carboxyl groups (for cation exchange).[3]
Solid-phase microextraction
Solid-phase microextraction (SPME), is a solid phase extraction technique that involves the use of a fiber coated with an extracting phase, that can be a liquid (polymer) or a solid (sorbent), which extracts different kinds of analytes (including both volatile and non-volatile) from different kinds of media, that can be in liquid or gas phase.[6] The quantity of analyte extracted by the fibre is proportional to its concentration in the sample as long as equilibrium is reached or, in case of short time pre-equilibrium, with help of convection or agitation.
References
- ↑ Hennion, Marie-Claire (1999). "Solid-phase extraction: method development, sorbents, and coupling with liquid chromatography". Journal of Chromatography A 856 (1–2): 3–54. doi:10.1016/S0021-9673(99)00832-8. ISSN 0021-9673. PMID 10526783.
- ↑ Augusto, Fabio; Hantao, Leandro W.; Mogollón, Noroska G.S.; Braga, Soraia C.G.N. (2013). "New materials and trends in sorbents for solid-phase extraction". TrAC Trends in Analytical Chemistry 43: 14–23. doi:10.1016/j.trac.2012.08.012. ISSN 0165-9936.
- ↑ 3.0 3.1 3.2 3.3 3.4 3.5 3.6 Supelco (1998), Guide to Solid Phase Extraction, http://www.sigmaaldrich.com/Graphics/Supelco/objects/4600/4538.pdf
- ↑ Abdel-Rehim, Mohamed (2011). "Microextraction by packed sorbent (MEPS): A tutorial". Analytica Chimica Acta 701 (2): 119–128. doi:10.1016/j.aca.2011.05.037. ISSN 0003-2670.
- ↑ M. Abdel-Rehim, AstraZeneca Application “Syringe for solid phase microextraction”, Current Patents Gazette, week 0310, WO 03019149, p. 77, (2003).
- ↑ Mitra, Somenath, ed (2003). Sample Preparation Techniques in Analytical Chemistry. Wiley-Interscience. p. 113. https://archive.org/details/samplepreparatio00mitr_147.
Further reading
- E. M. Thurman, M. S. Mills, Solid-Phase Extraction: Principles and Practice, Wiley-Interscience, 1998, ISBN:978-0-471-61422-7
- Nigel J.K. Simpson, Solid-Phase Extraction: Principles, Techniques, and Applications, CRC, 2000, ISBN:978-0-8247-0021-8
- James S. Fritz, Analytical Solid-Phase Extraction, Wiley-VCH, 1999, ISBN:978-0-471-24667-1
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