skip navigation

CrimeSolutions.gov

Add your conference to our Justice Events calendar

PUBLICATIONS

Register for Latest Research

Stay Informed
Register with NCJRS to receive NCJRS's biweekly e-newsletter JUSTINFO and additional periodic emails from NCJRS and the NCJRS federal sponsors that highlight the latest research published or sponsored by the Office of Justice Programs.

NCJRS Abstract

The document referenced below is part of the NCJRS Library collection. To conduct further searches of the collection, visit the NCJRS Abstracts Database. See the Obtain Documents page for direction on how to access resources online, via mail, through interlibrary loans, or in a local library.

 
  NCJ Number: NCJ 240685   Add to Shopping cart   Find in a Library
  Title: Development of a Thin Layer Chromatography Method for the Separation of Enantiomers Using Chiral Mobile Phase Additives
  Document URL: PDF 
  Author(s): Robyn L. Larson ; Kelly A. Howerter ; Jacob L. Easter
  Date Published: 12/2012
  Page Count: 55
  Annotation: This project’s objective was to develop an inexpensive and simple method for enantiomer determinations in controlled substances as an alternative to using mixed crystal test method, polarimetry, or more expensive instrumental methods.
  Abstract: Currently, the resolution of enantiomeric controlled substances is a problem for forensic chemists, since one enantiomer is usually controlled while the other enantiomer is not. The current project evaluated the use of chiral mobile-phase additives (CMAs) in thin layer chromatography (TLC) as an alternative method of enantiomer determination. Although TLC is not a novel technique its use as a method for resolving stereoisomeric controlled substances has not been widely examined. The research found that vancomycin was the most successful chiral mobile phase additive for producing enantiomeric separation, but inconsistently. Visualization of methorphan was troublesome because the multiple functional groups on vancomycin react with iodoplatinate, ceric sulfate, and the I2 vapors. Consequently, the concentration of vancomycin could not exceed 0.05M. The successful vancomycin mobile phase was always slightly opaque or cloudy. Each time the mobile phase was made, the opaqueness seemed to vary slightly and the separation seemed dependent on the appearance of the mobile phase. Even though the solution was cloudy, vancomycin did not come out of solution as a white precipitate as was observed with other mobile phases. Further research that uses vancomycin or another macrocyclic antibiotic for TLC separations may be useful. Although a suitable TLC method was not developed in this research, a more efficient, cost-effective method for differentiating stereoisomers may aid in coping with the increasing backlog in many laboratories by reducing the time required for such determinations. 14 tables and 17 references
  Main Term(s): Forensics/Forensic Sciences
  Index Term(s): Chromatography ; Drug analysis ; Investigative techniques ; NIJ final report ; NIJ grant-related documents
  Sponsoring Agency: National Institute of Justice (NIJ)
US Department of Justice
Office of Justice Programs
United States of America
  Grant Number: 2008-DN-BX-K140
  Sale Source: NCJRS Photocopy Services
Box 6000
Rockville, MD 20849-6000
United States of America
  Type: Report (Study/Research)
  Country: United States of America
  Language: English
   
  To cite this abstract, use the following link:
https://www.ncjrs.gov/App/Publications/abstract.aspx?ID=262765

*A link to the full-text document is provided whenever possible. For documents not available online, a link to the publisher's website is provided. Tell us how you use the NCJRS Library and Abstracts Database - send us your feedback.