کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
95406 160429 2015 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The use of a sulfonated capillary on chiral capillary electrophoresis/mass spectrometry of amphetamine-type stimulants for methamphetamine impurity profiling
ترجمه فارسی عنوان
استفاده از مویرگهای سولفونیک در الکتروفورز الکترولیز / جرمی کریل الکتروسرزمینی از محرک های نوع آمفتامینی برای پروفایل ناخالص متامفتامین
کلمات کلیدی
الکتروفورز مویرگی، طیف سنجی جرمی، تجزیه و تحلیل کریل، متامفتامین، مویرگی اصلاح شده شیمیایی
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• Chiral CE/MS/MS using a chemically modified capillary was developed.
• 8 amphetamine-type stimulants were well resolved within 60 min.
• The repeatability of migration times was obviously improved.
• Impurities in seized methamphetamine were clearly identified in this method.

Chiral capillary electrophoresis/tandem mass spectrometry (CE/MS/MS) using a chemically modified capillary containing sulfonated groups was developed for the following 8 amphetamine-type stimulants (ATS): amphetamine, methamphetamine (MA), norephedrine, norpseudoephedrine, ephedrine (EP), pseudoephedrine (pEP), dimethylamphetamine and methylephedrine. The running buffer was 10 mM formic acid containing 20 mM highly sulfated γ-cyclodextrin (pH 2.5) as the chiral selector. All 16 enantiomers were well resolved within 60 min, and precisely identified due to their characteristic mass spectra. Further, the RSDs of the migration times of the analytes were no more than 0.3% without any standardization. (1R,2S)-(−)-EP and (1S,2S)-(+)-pEP, which are important ATS impurities originating in the precursors, were added to a highly concentrated MA solution (1 mg/mL) and analyzed as mock samples for MA impurity analysis. Acceptable repeatability of the migration times of (−)-EP and (+)-pEP (ca. 0.3% RSDs) was still observed without interference from the large amount of MA. The limits of detection (LOD) of (−)-EP and (+)-pEP were approximately 2 μg/mL, therefore, their LOD as the impurity concentrations were calculated at about 0.2%. Seized MA samples were dissolved in water at a high concentration (1 mg/mL) and analyzed by this method. (−)-EP and (+)-pEP were clearly detected as impurities. Although these compounds had similar migration times and mass spectral patterns, the fine repeatability allowed easy identification of the impurities by a simple comparison of the absolute migration times of the specimens and those of authentic standards. This study is the first to report the use of a chemically modified capillary for the impurity profiling on CE/MS/MS.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Forensic Science International - Volume 249, April 2015, Pages 59–65
نویسندگان
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