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Recent developments in chiral capillary electrophoresis and applications of this technique to pharmaceutical and biomedical analysis.
Electrophoresis. 2001 Sep; 22(15):3107-30.E

Abstract

This paper provides an overview of the current status of chiral capillary electrophoresis (CE). The emphasis is placed on the application of CE in chiral separation of various racemic compounds. During the last two years about 280 papers, several review articles, and two entire issues, edited by S. Fanali (Electrophoresis 1999, 20, 2577-2798, and H. Nishi and S. Terabe (J. Chromatogr. A 2000, 879, 1-471.) have been devoted to chiral CE. Enantiomeric separations of various compounds, e.g., pharmaceuticals, drug candidates, drugs and related metabolites in biological fluids, amino acids, di- and tri peptides, pesticides and fungicides, have been performed using different chiral selectors. Native and derivatized cyclodextrins continue to be the most widely used chiral selectors. Other chiral selectors such as natural and synthetic chiral micelles, crown ethers, chiral ligands, proteins, oligo- and polysaccharides, and macrocyclic antibiotics have also been applied to chiral CE separations.

Authors+Show Affiliations

Medical Product Agency, Division of Biotechnology, Uppsala, Sweden. ahmad.amini@mpa.se

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

11589272

Citation

Amini, A. "Recent Developments in Chiral Capillary Electrophoresis and Applications of This Technique to Pharmaceutical and Biomedical Analysis." Electrophoresis, vol. 22, no. 15, 2001, pp. 3107-30.
Amini A. Recent developments in chiral capillary electrophoresis and applications of this technique to pharmaceutical and biomedical analysis. Electrophoresis. 2001;22(15):3107-30.
Amini, A. (2001). Recent developments in chiral capillary electrophoresis and applications of this technique to pharmaceutical and biomedical analysis. Electrophoresis, 22(15), 3107-30.
Amini A. Recent Developments in Chiral Capillary Electrophoresis and Applications of This Technique to Pharmaceutical and Biomedical Analysis. Electrophoresis. 2001;22(15):3107-30. PubMed PMID: 11589272.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Recent developments in chiral capillary electrophoresis and applications of this technique to pharmaceutical and biomedical analysis. A1 - Amini,A, PY - 2001/10/9/pubmed PY - 2002/2/22/medline PY - 2001/10/9/entrez SP - 3107 EP - 30 JF - Electrophoresis JO - Electrophoresis VL - 22 IS - 15 N2 - This paper provides an overview of the current status of chiral capillary electrophoresis (CE). The emphasis is placed on the application of CE in chiral separation of various racemic compounds. During the last two years about 280 papers, several review articles, and two entire issues, edited by S. Fanali (Electrophoresis 1999, 20, 2577-2798, and H. Nishi and S. Terabe (J. Chromatogr. A 2000, 879, 1-471.) have been devoted to chiral CE. Enantiomeric separations of various compounds, e.g., pharmaceuticals, drug candidates, drugs and related metabolites in biological fluids, amino acids, di- and tri peptides, pesticides and fungicides, have been performed using different chiral selectors. Native and derivatized cyclodextrins continue to be the most widely used chiral selectors. Other chiral selectors such as natural and synthetic chiral micelles, crown ethers, chiral ligands, proteins, oligo- and polysaccharides, and macrocyclic antibiotics have also been applied to chiral CE separations. SN - 0173-0835 UR - https://www.unboundmedicine.com/medline/citation/11589272/Recent_developments_in_chiral_capillary_electrophoresis_and_applications_of_this_technique_to_pharmaceutical_and_biomedical_analysis_ L2 - https://doi.org/10.1002/1522-2683(200109)22:15<3107::AID-ELPS3107>3.0.CO;2-Z DB - PRIME DP - Unbound Medicine ER -