Enantioseparation of new nucleoside analogs, related to d4T and acyclovir, by chiral capillary electrophoresis using highly sulfated β-cyclodextrins

Electrophoresis

Volumn 25, Issue 3, 2004, Pages 444-453

  Lipka, Emmanuelle ^a   Daniel, Cecile ^a   Vaccher, Marie Pierre ^a   Glaçon, Virginie ^a   Ewing, David ^b   Mackenzie, Graham ^b   Len, Christophe ^c   Bonte, Jean Paul ^a   Vaccher, Claude ^a,d  

^a UNIV LILLE   (France)

^b UNIVERSITY OF HULL   (United Kingdom)

^c UNIVERSITÉ DE PICARDIE JULES VERNE   (France)

^d NONE   (France)

Author keywords

Chiral capillary electrophoresis; Enantiomeric purity; Highly sulfated cyclodextrins; Nucleosides

Indexed keywords

ANTIVIRAL AGENTS; BIOMOLECULES; CAPILLARY ELECTROPHORESIS; CHIRALITY; CYCLODEXTRINS; ENANTIOMERS; POLYETHYLENE OXIDES; STEREOCHEMISTRY;

BASELINE SEPARATION; CHIRAL CAPILLARY ELECTROPHORESIS; CHIRAL SELECTOR; ENANTIOMERIC PURITY; ENANTIOMERIC RESOLUTION; ENANTIOSEPARATIONS; HIGHLY SULPHATED CYCLODEXTRIN; NUCLEOSIDE; NUCLEOSIDE ANALOGS; SULFATED CYCLODEXTRINS;

VIRUSES;

2',3' DIDEOXY 2',3' DIDEHYDROCYTOSINE; ACICLOVIR; ACYCLIC NUCLEOSIDE; ADENINE; ANTIVIRUS AGENT; AZATHIOPRINE; BETA CYCLODEXTRIN DERIVATIVE; BUFFER; CARBOVIR; CYTOSINE; DIDANOSINE; GUANINE; LAMIVUDINE; MACROGOL; NUCLEOSIDE ANALOG; ORGANIC COMPOUND; PHOSPHATE; STAVUDINE; SULFATE; THYMINE; UNCLASSIFIED DRUG; URACIL; ZIDOVUDINE;

ARTICLE; CAPILLARY ZONE ELECTROPHORESIS; CHEMICAL PROCEDURES; CHIRALITY; COMPLEX FORMATION; CONTROLLED STUDY; DRUG IMPURITY; DRUG STRUCTURE; ELECTRIC POTENTIAL; ENANTIOSELECTIVITY; MATERIAL COATING; PH; SEPARATION TECHNIQUE; SULFATION; TEMPERATURE;

EID: 1342283695     PISSN: 01730835     EISSN: None     Source Type: Journal    
DOI: 10.1002/elps.200305706     Document Type: Article

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