Journal
JOURNAL OF CHROMATOGRAPHY A
Volume 1643, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.chroma.2021.462088
Keywords
Chloromethyl phenylcarbamate-based chiral stationary phases; High-resolution mass spectrometry; New Psychoactive Substances (NPSs); Ionic additives
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Fentanyl analogues are commonly used in therapy, but the rise in illicitly synthesized fentanyl derivatives has led to hospitalizations and deaths. Chromatographic methods are essential for differentiating enantiomers of fentanyl derivatives. This study successfully separated four fentanyl derivatives' enantiomers under polar-ionic conditions.
Fentanyl analogues used in therapy and a range of highly potent non-pharmaceutical fentanyl derivatives are subject to international control, as the latter are increasingly being synthesized illicitly and sold as 'synthetic heroin', or mixed with heroin. A significant number of hospitalizations and deaths have been reported in the EU and USA following the use of illicitly synthesized fentanyl derivatives. It has been unequivocally demonstrated that the enantiomers of fentanyl derivatives exhibit different pharmaco-toxicological profiles, which makes crucial to avail of suitable analytical methods enabling investigations at a stereochemical level. Chromatographic methods useful to discriminate the enantioseparation of fentanyls and their derivatives are still missing in the literature. This is the first study in which the enantioseparation of four fentanyl derivatives, that is, (+/-)-trans-3-methyl norfentanyl, (+/-)-cis-3-methyl norfentanyl, beta-hydroxyfentanyl, and beta-hydroxythiofentanyl, has been obtained under polar-ionic conditions. Indeed, the use of ACN-based mobile phases with minor amounts of either 2-propanol or ethanol (plus diethylamine and formic acid as ionic additives) allowed obtaining enantioseparation and enantioresolution factors up to 1.83 and 7.02, respectively. For the study, the two chiral stationary phases cellulose tris(3-chloro-4-methylphenylcarbamate) and cellulose tris(4-chloro-3-methylphenylcarbamate) were used, displaying a remarkably different performance towards the enantioseparation of (+/-)-cis-3-methyl norfentanyl. Chiral LC analyses with a high-resolution mass spectrometry detector were also carried out in order to confirm the obtained data and demonstrate the suitability and compatibility of the optimized mobile phases with mass spectrometric systems. (C) 2021 Elsevier B.V. All rights reserved.
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