Determination of psilocybin in hallucinogenic mushrooms by reversed-phase liquid chromatography with fluorescence detection
Kimie Saito, Toshimasa Toyo’oka, Masaru Kato, Takeshi Fukushima, Osamu Shirota, Yukihiro Goda
Abstract
The determination of psilocybin was carried out by reversed-phase liquid chromatography (HPLC) with fluorescence (FL) detection. Psilocybin was labeled with 5-dimethylaminonaphthalene-1-[N-(2-aminoethyl)]sulfonamide (DNS-ED) at 60 ◦ C for 4 h in the presence of 1- ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) as the activation reagent. The resulting derivative was separated on a Mightysil RP-18 GP column (150 mm × 4.6 mm, i.d. 3 m) with the mixture of 50 mM ammonium acetate (AcONH4 ) and CH3 CN, and detected at 539 nm (excitation at 321 nm). The structure of the derivative was identified by HPLC–ESI-MS. A good linear relation of the calibration curve of psilocybin was observed under the proposed conditions for labeling, separation and detection. The quantification limit was 4.4 ng in 1 mg dried mushroom. The proposed procedure was successfully used for the determination of psilocybin in real samples. The contents of psilocybin in six magic mushrooms by the proposed HPLC–FL method were less than 20.0 ng in 1 mg dried samples.
© 2004 Elsevier B.V. All rights reserved.Keywords: Psilocybin; Hallucinogenic mushroom; Fluorescence labeling; Reversed-phase HPLC
Kimie Saito, Toshimasa Toyo’oka, Masaru Kato, Takeshi Fukushima, Osamu Shirota, Yukihiro Goda
Abstract
The determination of psilocybin was carried out by reversed-phase liquid chromatography (HPLC) with fluorescence (FL) detection. Psilocybin was labeled with 5-dimethylaminonaphthalene-1-[N-(2-aminoethyl)]sulfonamide (DNS-ED) at 60 ◦ C for 4 h in the presence of 1- ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) as the activation reagent. The resulting derivative was separated on a Mightysil RP-18 GP column (150 mm × 4.6 mm, i.d. 3 m) with the mixture of 50 mM ammonium acetate (AcONH4 ) and CH3 CN, and detected at 539 nm (excitation at 321 nm). The structure of the derivative was identified by HPLC–ESI-MS. A good linear relation of the calibration curve of psilocybin was observed under the proposed conditions for labeling, separation and detection. The quantification limit was 4.4 ng in 1 mg dried mushroom. The proposed procedure was successfully used for the determination of psilocybin in real samples. The contents of psilocybin in six magic mushrooms by the proposed HPLC–FL method were less than 20.0 ng in 1 mg dried samples.
© 2004 Elsevier B.V. All rights reserved.Keywords: Psilocybin; Hallucinogenic mushroom; Fluorescence labeling; Reversed-phase HPLC
