TY - JOUR
T1 - Use of sulfated cyclofructan 6 and sulfated cyclodextrins for the chiral separation of four basic pharmaceuticals by capillary electrophoresis
AU - Zhang, Yi Jun
AU - Huang, Ming Xian
AU - Zhang, Yu Ping
AU - Armstrong, Daniel Wayne
AU - Breitbach, Zachary S.
AU - Ryoo, Jae Jeong
PY - 2013/11
Y1 - 2013/11
N2 - Sulfated cyclofructan 6 (S-CF6) and sulfated cyclodextrins (S-α-, β-, γ-CDs) are highly selective chiral selectors for the enantioseparation of basic solutes. In this study, S-CF6 was introduced for the enantiomeric separation of four basic pharmaceuticals (including tamsulosin, tiropramide, bupivacaine, and norephedrine) by capillary electrophoresis (CE), and the enantiomeric separation performance was compared with S-α-, β-, γ-CDs. The effects of the chiral selector type, chiral selector concentration, operating voltage, and column temperature were examined and optimized. Excellent resolutions were obtained for all solutes on these chiral selectors. Chirality 25:735-742, 2013.
AB - Sulfated cyclofructan 6 (S-CF6) and sulfated cyclodextrins (S-α-, β-, γ-CDs) are highly selective chiral selectors for the enantioseparation of basic solutes. In this study, S-CF6 was introduced for the enantiomeric separation of four basic pharmaceuticals (including tamsulosin, tiropramide, bupivacaine, and norephedrine) by capillary electrophoresis (CE), and the enantiomeric separation performance was compared with S-α-, β-, γ-CDs. The effects of the chiral selector type, chiral selector concentration, operating voltage, and column temperature were examined and optimized. Excellent resolutions were obtained for all solutes on these chiral selectors. Chirality 25:735-742, 2013.
KW - basic pharmaceuticals
KW - capillary electrophoresis
KW - chiral separations
KW - sulfated cyclodextrins
KW - sulfated cyclofructan 6
UR - http://www.scopus.com/inward/record.url?scp=84886640616&partnerID=8YFLogxK
U2 - 10.1002/chir.22206
DO - 10.1002/chir.22206
M3 - Article
C2 - 23939835
AN - SCOPUS:84886640616
SN - 0899-0042
VL - 25
SP - 735
EP - 742
JO - Chirality
JF - Chirality
IS - 11
ER -