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Stig Pedersen-Bjergaard

Department of Pharmacy, University of Oslo, P.O. Box 1068 Blindern, 0316, Oslo, Norway; Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark.

2 papers in the library · 43 citations · publishing 2017-2024

Papers

Parallel artificial liquid membrane extraction of new psychoactive substances in plasma and whole blood.

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences March 24, 2017 Linda Vårdal, Hilde-Merete Askildsen, Astrid Gjelstad et al. 34 citations

Parallel artificial liquid membrane extraction (PALME) combined with ultra-high performance liquid chromatography-mass spectrometry can screen for new psychoactive substances (NPS) in plasma and whole blood. Eleven NPS, including MDAI, methylone, and MDPV, were extracted from alkalized donor solutions across an organic liquid membrane into an acidic acceptor solution using a pH gradient. For plasma, the donor solution contained 125 µL plasma, 115 µL 40 mM NaOH, and 10 µL internal standard; for whole blood, it contained 100 µL blood, 50 µL water, 75 µL 80 mM NaOH, and 25 µL internal standard. Extraction used 5 µL dodecyl acetate with 1% trioctylamine as the membrane and 50 µL 20 mM formic acid as the acceptor, agitated at 900 rpm for 120 minutes. Validation met FDA guidelines.

Solvent-free parallel artificial liquid membrane extraction for drugs of abuse in plasma samples using LC-MS/MS.

Analytica chimica acta May 1, 2024 André Luis Fabris, Stig Pedersen-Bjergaard, Elisabeth Leere Øiestad et al. 9 citations

A 96-well plate extraction method called parallel artificial liquid membrane extraction (PALME) can be made greener by replacing organic solvents with an essential oil. Fourteen essential oils were tested; the blend smart & sassy gave the best recovery for multiple drugs of abuse in plasma, including amphetamines, synthetic cathinones, and designer benzodiazepines. After optimization, the method achieved a linear range of 1-100 ng/mL, accuracy within ±16.4%, and limits of detection between 0.1 and 0.75 ng/mL. The technique eliminated hazardous organic solvents, provided effective sample clean-up, and met international validation guidelines, offering a sustainable tool for toxicological analysis.