Capillary zone electrophoretic chiral discrimination using 6-O-(2-hydroxy-3-trimethylammonioprophyl)-β-cyclodextrin as a chiral selector

Electrophoresis

Volumn 27, Issue 4, 2006, Pages 872-879

  Lin, Xiuli ^a   Zhao, Minggang ^a   Qi, Xinyu ^b   Zhu, Chenfu ^a   Hao, Aiyou ^a  

^a SHANDONG UNIVERSITY   (China)

^b Chemical Industry Research Institute of Shandong Province   (China)

Author keywords

Capillary electrophoresis; Chiral drugs; Cyclodextrin; Enantiomer separation; Cyclodextrin derivative

Indexed keywords

CYCLODEXTRINS; DRUG DELIVERY; ELECTROLYTES; ENANTIOMERS;

CAPILLARY ZONE; CHIRAL DISCRIMINATION; CHIRAL DRUGS; CHIRAL SELECTOR; CYCLODEXTRIN DERIVATIVES; ENANTIOMERS SEPARATION; SYNTHESISED; WATERSOLUBLE; Β-CD; Β-CYCLODEXTRIN DERIVATIVE;

CAPILLARY ELECTROPHORESIS;

3 PHENYLLACTIC ACID; 6 O (2 HYDROXY 3 TRIMETHYLAMMONIOPROPYL) BETA CYCLODEXTRIN; ABSCISIC ACID; ARYLPROPIONIC ACID DERIVATIVE; BETA CYCLODEXTRIN; CYCLODEXTRIN DERIVATIVE; ELECTROLYTE; FLURBIPROFEN; IBUPROFEN; INDOPROFEN; KETOPROFEN; LACTIC ACID DERIVATIVE; MANDELIC ACID; MUSCARINIC RECEPTOR BLOCKING AGENT; NAPROXEN; OFLOXACIN; PHOSPHATE; QUATERNARY AMMONIUM DERIVATIVE; TROPIC ACID; UNCLASSIFIED DRUG; WARFARIN;

ARTICLE; CAPILLARY ZONE ELECTROPHORESIS; CHIRALITY; COMPARATIVE STUDY; CONCENTRATION RESPONSE; DRUG DETERMINATION; DRUG STRUCTURE; ELECTROPHORETIC MOBILITY; ENANTIOMER; PH; RACEMIC MIXTURE; SENSITIVITY AND SPECIFICITY; SEPARATION TECHNIQUE; SUBSTITUTION REACTION; SYNTHESIS;

EID: 33644681523     PISSN: 01730835     EISSN: 15222683     Source Type: Journal    
DOI: 10.1002/elps.200500657     Document Type: Article

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