The following table summarizes the foregoing discussion of the modes of SPE:
Summary of Utility and Practice of Principal LC Modes for Solid-Phase Extraction [SPE]
Reversed Phase | Normal Phase | Ion Exchange | ||
Analyte | Moderate to low polarity | Low to high polarity/neutral | Charged or Ionizable | |
Separation Mechanism | Separation based on hydrophobicity | Separation based on polarity | Separation based on charge | |
Sample Matrix | Aqueous | Non-polar organic solvent | Aqueous/ Low ionic strength | |
Condition/ Equilibrate SPE Sorbent | 1. Solvate with polar organic 2. Water | Non-polar organic | Low ionic strength buffer | |
Preliminary Wash Step | Aqueous/buffer | Non-polar organic | Low ionic strength buffer | |
Elution Steps | Increase polar organic content | Increase eluotropic strength of organic solvent mixture | Stronger buffers - ionic strength or pH to neutralize the charge | |
AX [Anion Exchange] | CX [Cation Exchange] | |||
Sorbent Functionality | C18, tC18, C8, tC2, CN, NH2, HLB, RDX, Rxn RP | Silica, Alumina, Florisil, Diol, CN, NH2 | Accell Plus QMA, NH2, SAX, MAX, WAX | Accell Plus CM, SCX, MCX, WCX, Rxn CX |
Sorbent Surface Polarity | Low to Medium | High to Medium | High | High |
Typical Solvent Polarity Range | High to Medium | Low to Medium | High | High |
Typical Sample Loading Solvent | Water, low strength buffer | Hexane, chloroform, methylene chloride | Water, low strength buffer | Water, low strength buffer |
Typical Elution Solvent | CH3OH/water, CH3CN/water | Ethyl acetate, acetone, CH3CN | Buffers, salts with high ionic strength, increase pH | Buffers, salts with high ionic strength, decrease pH |
Sample Elution Order | Most polar sample components first | Least polar sample components first | Most weakly ionized sample component first | Most weakly ionized sample component first |
Mobile Phase Solvent Change Required to Elute Compounds | Decrease solvent polarity | Increase solvent polarity | Increase ionic strength or increase pH | Increase ionic strength, or lower pH |
This has been a brief introduction to sample enrichment and purification using solid-phase extraction [SPE]. The best way to start using SPE is to first learn what others have done with analytes and/or matrices similar to those of interest to you. You will find > 7,700 references to the use of SPE in the Resource Library on waters.com. Fill in the blank with a partial compound or matrix name in the following search phrase:
“Sep-Pak” OR “Oasis” AND ______*
NOTE: Rather than risk a spelling error, use an asterisk [*] with a root name for best results. Using this same search string, even more references [> 60,000] may be found on GOOGLE Scholar.
Further reading:
J.C. Arsenault and P.D. McDonald, Beginners Guide to Liquid Chromatography, Waters [2007]; Order P/N 715001531 on waters.com
P.D. McDonald and E.S.P. Bouvier, A Sample Preparation Primer and Guide to Solid-Phase Extraction Methods Development, Waters [2001] Search for WA20300 on waters.com
Waters, Purity by SPE [2008]; Search for 720001692en on waters.com
U.D. Neue, P.D. McDonald, Topics in Solid-Phase Extraction. Part 1. Ion Suppression in LC/MS Analysis: A Review. Strategies for its elimination by well-designed, multidimensional solid-phase extraction [SPE] protocols and methods for its quantitative assessment [2005]; Search for 720001273en on waters.com
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