| Literature DB >> 28456284 |
Ludovit Skultety1, Petr Frycak2, Changling Qiu3, Jonathan Smuts4, Lindsey Shear-Laude4, Karel Lemr5, James X Mao3, Peter Kroll3, Kevin A Schug3, Angelica Szewczak6, Cory Vaught6, Ira Lurie6, Vladimir Havlicek7.
Abstract
Distinguishing isomeric representatives of "bath salts", "plant food", "spice", or "legal high" remains a challenge for analytical chemistry. In this work, we used vacuum ultraviolet spectroscopy combined with gas chromatography to address this issue on a set of forty-three designer drugs. All compounds, including many isomers, returned differentiable vacuum ultraviolet/ultraviolet spectra. The pair of 3- and 4-fluoromethcathinones (m/z 181.0903), as well as the methoxetamine/meperidine/ethylphenidate (m/z 247.1572) triad, provided very distinctive vacuum ultraviolet spectral features. On the contrary, spectra of 4-methylethcathinone, 4-ethylmethcathinone, 3,4-dimethylmethcathinone triad (m/z 191.1310) displayed much higher similarities. Their resolution was possible only if pure standards were probed. A similar situation occurred with the ethylone and butylone pair (m/z 221.1052). On the other hand, majority of forty-three drugs was successfully separated by gas chromatography. The detection limits for all the drug standards were in the 2-4 ng range (on-column amount), which is sufficient for determinations of seized drugs during forensics analysis. Further, state-of-the-art time-dependent density functional theory was evaluated for computation of theoretical absorption spectra in the 125-240 nm range as a complementary tool.Entities:
Keywords: Bath salts; Fourier transform ion cyclotron resonance; Gas phase absorption; Isomeric drugs; Time-dependent density functional theory; VUV absorption spectroscopy
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Year: 2017 PMID: 28456284 DOI: 10.1016/j.aca.2017.03.023
Source DB: PubMed Journal: Anal Chim Acta ISSN: 0003-2670 Impact factor: 6.558