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Strategies for the capillary electrophoretic separation of indole alkaloids in Psilocybe semilanceata.

Stig Pedersen-Bjergaard, K E Rasmussen, Ellen Sannes

Electrophoresis January 1998 DOI: 10.1002/elps.1150190107 (opens in new tab)

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AI-extracted from the abstract
Characteristics Peer reviewed
Key points Derivatization with propyl chloroformate followed by capillary zone electrophoresis at pH 11.5 supports identification of psilocybin and baeocystin, whereas micellar electrokinetic chromatography did not resolve them. Psilocin comigrates with the electroosmotic flow at pH 11.5, but reducing the running buffer pH to 7.2 enhances its electrophoretic mobility.

Abstract

While the hallucinogenic mushrooms Psilocybe semilanceata have previously been analyzed for the indole alkaloids psilocybin and baeocystin by capillary zone electrophoresis (CZE) at pH 11.5, the present work focused on the development of an alternative and complementary capillary electrophoretic method for their identification. Owing to their structural similarity and zwitterionic nature, the compounds were difficult to resolve based on different interactions with cationic or anionic micelles. However, while the attempts with micellar electrokinetic chromatography (MEKC) were unsuccessful, rapid derivatization with propyl chloroformate and reanalysis by CZE at pH 11.5 was effective to support identification of the two indole alkaloids. Psilocin was difficult to analyze by CZE at pH 11.5 owing to comigration with the electroosmotic flow. For this compound, the pH of the running buffer was reduced to 7.2 to effectively enhance the electrophoretic mobility.

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