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enantioresolution of amphetamine metamphetamine and deprenyl selegiline by lc gc and ce n.
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Enantioresolution of Amphetamine, Metamphetamine, and Deprenyl ( Selegiline) by LC, GC, and CE PowerPoint Presentation
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Enantioresolution of Amphetamine, Metamphetamine, and Deprenyl ( Selegiline) by LC, GC, and CE

Enantioresolution of Amphetamine, Metamphetamine, and Deprenyl ( Selegiline) by LC, GC, and CE

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Enantioresolution of Amphetamine, Metamphetamine, and Deprenyl ( Selegiline) by LC, GC, and CE

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  1. Enantioresolution of Amphetamine, Metamphetamine, and Deprenyl ( Selegiline) by LC, GC, and CE การแยกenantiomeric (R, S, (+), (-)form)ของ amphetamine,methamphetamine,และselegiline ด้วยวิธีLC, GCและCE นำเสนอโดยน.ส. อรทัย กฤษณานุวัฒน์ รหัสนักศึกษา 51312336

  2. จุดประสงค์ของงานวิจัยจุดประสงค์ของงานวิจัย

  3. Enantiomer ? • - Sterioisomer • - Isomer are two or more compounds • with the same molecular composition but different • Structures result in different properties • Example of structural isomer (a) butane and (b) isobutane

  4. *Stereoisomers describes compounds with the same Molecularformula and chemical structure but the atom are orientatedin different direction. *There are two isomer each a mirror image of the other call enantiomers These two molecules are stereoisomer or enantiomer

  5. H2N H H NH2 CH3 CH3 l-Amphetamine d-Amphetamine CH3NH H H NHCH3 CH3 CH3 l-Methamphetamine d-Methamphetamine *The mean of d-,l-, (+) , (-) ,R- and S- - if an isomer rotates the plane clockwise label (+) termed d - its counter is label (-) termed l Structures of enantiomers of amphetamine and methamphetamine

  6. * Amphetamine , methamphetamine and selegiline are chiral compound

  7. * The legimate uses of amphetamine and • methamphetaminehyperactivityand treatment • of exogenous obesity • * The rapid and effective enantioresolution is • importantfor pharmacological, toxicological, • forensic studies and product quality control • * Capillary electrophoresis (CE) may be the best • for the rapid analysis of small amounts of pure • compound • * Greater sensitivity and reproducibility of GC or • LC may be needed when analyzing low levels • of a compound

  8. *Materials And Method - LC and CE Fisher Scientific - LC  Cyclobond  2000 LC column  Cyclobond  2000 RSP LC column  Cyclobond  2000 DMPLC column  Cyclobond  2000 RN LC column  Cyclobond  2000 SN LC column - GC  Chiraldex - DM capillary GC column  Chiraldex G-PN GC column

  9. Result and Discussion  Derivatized cyclodextrin chiral stationary phase methamphetamine pseudoephedrine amphetamine ephedrine Chiraldex G-PN column

  10. Selegiline Chiraldex - DM column

  11. * The ability to rapid determine enantiomeric rations of methamphetamine and its possible precursors in a single run can be useful for forensic identification * IT is not necessary for routine pharmaceutical analyses

  12. AM LC MA MA CE AM

  13. Selegiline

  14. o-phthaldehyde (OPA) • naphthalene- dialdehyde (NDA) • aromatic anhydrides (AA) • 9- fluorenylmethylchloroformate (FMOC) • 6- aminoquinolyl-N-hydroxysuccinimidyl • carbamate (AQC) • For chiral amines and amino acid where • enantioseparations are also involved AQC, • AA and FMOC Fluorescent taggingagent

  15. Reversed- organic mode Polar- organic mode - LC enantiomeric separation of AQC-amphetamine tagging agent

  16. - LC separation of AQC-methamphetamine

  17. Conclusions • - Clearly, different approaches are useful for • biological assay , forensic assays and QC • of a pharmaceutical product • One chiral separation method may be • superior to another

  18. จบการนำเสนอ