Solid-phase microextraction

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Solid-phase microextraction sampling

Solid phase microextraction, or SPME, is a solid phase extraction sampling technique that involves the use of a fiber coated with an extracting phase, that can be a liquid (polymer) or a solid (sorbent),[1] 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.[2] 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.

Analysis

After extraction, the SPME fiber is transferred to the injection port of separating instruments, such as a gas chromatography and mass spectrometry,[3] where desorption of the analyte takes place and analysis is carried out.

Advantages

The attraction of SPME is that the extraction is fast, simple, can be done usually without solvents, and detection limits can reach parts per trillion (ppt) levels for certain compounds. SPME also has great potential for field applications; on-site sampling can be done even by nonscientists without the need to have gas chromatography-mass spectrometry equipment at each location. When properly stored, samples can be analyzed days later in the laboratory without significant loss of volatiles.[citation needed]

Fiber Coatings

The coating on the SPME fiber can be selected to improve sensitivity for specific analytes of interest; ideally the sorbent layer will have a high affinity for the target analytes.[4][5] There are many commercially available SPME fiber coatings that are combinations of polydimethylsiloxane, divinylbenzene, Carboxen, polyacrylate, and polyethylene glycol.[6][7] However, one downside to many of the commercially available SPME fibers is that they tend to be physically brittle due to their composition.[5] Depending on the characteristics of the target analytes, certain properties of the coating improve extraction such as polarity, thickness, and surface area.[4][8] The sample matrix can also influence the fiber coating selection. Based on the sample and analytes of interest, the fiber may need to tolerate direct immersion as opposed to a headspace extraction.[6]

References

  1. ↑ Spietelun, Agata; Pilarczyk, Michał; Kloskowski, Adam; Namieśnik, Jacek (2010). "Current trends in solid-phase microextraction (SPME) fibre coatings". Chemical Society Reviews 39 (11): 4524–37. doi:10.1039/c003335a. ISSN 0306-0012. PMID 20882243. 
  2. ↑ Mitra, Somenath, ed (2003). Sample Preparation Techniques in Analytical Chemistry. Wiley-Interscience. p. 113. 
  3. ↑ Vas, György; Vékey, Károly (2004). "Solid-phase microextraction: a powerful sample preparation tool prior to mass spectrometric analysis". Journal of Mass Spectrometry 39 (3): 233–254. doi:10.1002/jms.606. ISSN 1076-5174. PMID 15039931. Bibcode: 2004JMSp...39..233V. 
  4. ↑ 4.0 4.1 Spietelun, Agata; Pilarczyk, Michał; Kloskowski, Adam; Namieśnik, Jacek (2010). "Current trends in solid-phase microextraction (SPME) fibre coatings" (in en). Chemical Society Reviews 39 (11): 4524. doi:10.1039/c003335a. ISSN 0306-0012. PMID 20882243. 
  5. ↑ 5.0 5.1 Spietelun, Agata; Kloskowski, Adam; Chrzanowski, Wojciech; Namieśnik, Jacek (2012-12-28). "Understanding Solid-Phase Microextraction: Key Factors Influencing the Extraction Process and Trends in Improving the Technique" (in EN). Chemical Reviews 113 (3): 1667–1685. doi:10.1021/cr300148j. ISSN 0009-2665. PMID 23273266. 
  6. ↑ 6.0 6.1 Reyes-Garcés, Nathaly; Gionfriddo, Emanuela; Gómez-Ríos, German Augusto; Alam, Md. Nazmul; Boyacı, Ezel; Bojko, Barbara; Singh, Varoon; Grandy, Jonathan et al. (2017-12-14). "Advances in Solid Phase Microextraction and Perspective on Future Directions" (in EN). Analytical Chemistry 90 (1): 302–360. doi:10.1021/acs.analchem.7b04502. ISSN 0003-2700. PMID 29116756. 
  7. ↑ Kumar, Ashwini; Gaurav; Malik, Ashok Kumar; Tewary, Dhananjay Kumar; Singh, Baldev (2008-03-03). "A review on development of solid phase microextraction fibers by sol–gel methods and their applications". Analytica Chimica Acta 610 (1): 1–14. doi:10.1016/j.aca.2008.01.028. ISSN 0003-2670. PMID 18267134. 
  8. ↑ Wardencki, Waldemar; Michulec, Magdalena; Curylo, Janusz (2004-07-29). "A review of theoretical and practical aspects of solid-phase microextraction in food analysis" (in en). International Journal of Food Science and Technology 39 (7): 703–717. doi:10.1111/j.1365-2621.2004.00839.x. ISSN 0950-5423. 

Further reading

  • Janusz Pawliszyn: Handbook of Solid Phase Microextraction, Chemical Industry Press, 2009.
  • Pawliszyn J.: Solid Phase Microextraction: Theory and Practice, Wiley-VCH, 1997.
  • Pawliszyn J.: Applications of Solid Phase Microextraction, Royal Society of Chemistry, 1999.

Interactive lectures



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