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- W4300688231 abstract "During this study, a simple and easy-to-prepare electrophoretic method was developed for the enantioseparation of amphetamine and cathinone derivatives. Different types of β-cyclodextrin and cyclofructan-based chiral selectors (CSs), both native and derivatized, were utilized, and the most effective ones, in terms of resolution and analysis time, were identified. In addition, several electrophoretic parameters, such as background electrolyte concentration and pH, and CS concentration, were examined to optimize the separation conditions. Under the optimal electrophoretic conditions, 10 psychoactive substances were enantiomerically separated using 1 mM sulfated cyclofructan-6 (SCF-6) for the amphetamine derivatives and 1 mM sulfated cyclofructan-7 (SCF-7) for the cathinone derivatives dissolved in an aqueous solution of 20-mM monobasic sodium phosphate at pH 2.5, a temperature of 25°C, and an applied voltage of 25 kV. In addition, the method was validated by estimating the intra- and interday precision." @default.
- W4300688231 created "2022-10-04" @default.
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- W4300688231 date "2022-10-17" @default.
- W4300688231 modified "2023-10-12" @default.
- W4300688231 title "Evaluation of cyclodextrin‐ and cyclofructan‐based chiral selectors for the enantioseparation of psychoactive substances in capillary electrophoresis" @default.
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- W4300688231 doi "https://doi.org/10.1002/elps.202200182" @default.
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