Kong D, Yang W, Duan K, Cui Y, Xing S, Zhang X, Sheng X, Zhang L
Capillary electrophoretic enantioseparation of m-nisoldipine using two different beta-cyclodextrins. [JOURNAL ARTICLE]
J Sep Sci 2009 Sep 10; 32(18):3178-3183.
The methods for the enantioseparation of m-nisoldipine, a new 1,4-dihydropyridine calcium ion antagonist, were developed. The elaborated methods of m-nisoldipine enantiomers separation were successfully performed using an anionic CD-sulfobutyl ether-beta-CD (SBE-beta-CD) or carboxymethyl-beta-CD as chiral selector. However, the results indicated that SBE-beta-CD was a better chiral selector for enantioseparation of the neutral m-nisoldipine. Furthermore, comparing the two SBE-beta-CDs, the derivative with a higher degree of substitution (DS) of 7.0 induced better enantioresolution than the one with low DS (4.0). In addition, possible chiral recognition mechanisms of dihydropyridines were discussed.
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