The goals of this proposed research are to develop the first widely applicable multimodal chiral stationary phase, development of novel enantiomeric separation methods for compounds that cannot be resolved directly by any known means (particularly those containing few, if any functional groups) and to understand the chiral recognition and racemic separation process. More specifically, our work will focus on ordered media (i.e., CD derivatives, micelles, and so on). The principal types of compounds that will be studied are drugs and related compounds of interest to the biomedical community as well as compounds of environmental importance (e.g., pesticides, pheromones, etc.). This work is of great value to the health and welfare of the population as a whole because nearly 30% of all prescribed drugs consist of racemic mixtures. Other """"""""natural-products"""""""" frequently contain significant amounts of """"""""enantiomeric impurities"""""""" as well. These result from racemization during isolation and purification. These chiral, enantiomeric impurities frequently are responsible for a drug's side effects or can limit the effectiveness of the desired isomer. In addition to developing and understanding new analytical methods we will develop effective preparative-scale methods for resolving enantiomers. Preliminary data suggests that these have a high probability of success. The analytical liquid and gas chromatographic methods will make use of several unusual CD derivatives and a number of chiral bile acids. Three very different approaches will be used for large-scale separations. These are: chiral hollow-fiber membranes, centrifugal countercurrent chromatography and chiral foam flotation. A significant portion of this work will involve the use of statistical mechanical calculations and calorimetry to refine and evaluate our models and results. X-ray crystallography will allow structure determination of chiral selectors (such as derivatized cyclodextrins, CDs) and complexes. These can be projected and manipulated through the use of computer graphics and energy minimization calculations.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM036292-06
Application #
3289971
Study Section
Metallobiochemistry Study Section (BMT)
Project Start
1987-09-01
Project End
1994-06-30
Budget Start
1992-07-01
Budget End
1993-06-30
Support Year
6
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of Missouri-Rolla
Department
Type
Schools of Arts and Sciences
DUNS #
804883767
City
Rolla
State
MO
Country
United States
Zip Code
65409
Peter, A; Torok, G; Armstrong, D W (1998) High-performance liquid chromatographic separation of enantiomers of unusual amino acids on a teicoplanin chiral stationary phase. J Chromatogr A 793:283-96
Armstrong, D W; Gasper, M P; Rundlett, K L (1995) Highly enantioselective capillary electrophoretic separations with dilute solutions of the macrocyclic antibiotic ristocetin A. J Chromatogr A 689:285-304
Berthod, A; Zhou, E Y; Le, K et al. (1995) Determination and use of Rohrschneider-McReynolds constants for chiral stationary phases used in capillary gas chromatography. Anal Chem 67:849-57
Pawlowska, M; Zukowski, J; Armstrong, D W (1994) Sensitive enantiomeric separation of aliphatic and aromatic amines using aromatic anhydrides as nonchiral derivatizing agents. J Chromatogr A 666:485-91
Armstrong, D W; Rundlett, K; Reid 3rd, G L (1994) Use of a macrocyclic antibiotic, rifamycin B, and indirect detection for the resolution of racemic amino alcohols by CE. Anal Chem 66:1690-5
Pawlowska, M; Armstrong, D W (1994) Evaluation of enantiomeric purity of selected amino acids in honey. Chirality 6:270-6
Armstrong, D W; Rundlett, K L; Chen, J R (1994) Evaluation of the macrocyclic antibiotic vancomycin as a chiral selector for capillary electrophoresis. Chirality 6:496-509
Rundlett, K L; Armstrong, D W (1994) Evaluation of free D-glutamate in processed foods. Chirality 6:277-82
Pawlowska, M; Chen, S; Armstrong, D W (1993) Enantiomeric separation of fluorescent, 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate, tagged amino acids. J Chromatogr 641:257-65
Armstrong, D W; Zukowski, J; Ercal, N et al. (1993) Stereochemistry of pipecolic acid found in the urine and plasma of subjects with peroxisomal deficiencies. J Pharm Biomed Anal 11:881-6

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