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以单一对映体硫酸化环糊精作为手性选择剂,在环糊精修饰的毛细管区带电泳中对吩噻嗪类药物进行对映体拆分。

Enantioseparation of phenothiazines in CD-modified CZE using single isomer sulfated CD as a chiral selector.

作者信息

Liao Wei-Ssu, Lin Chen-Hsing, Chen Chih-Yu, Kuo Chia-Ming, Liu Yu-Chih, Wu Jong-Chang, Lin Ching-Erh

机构信息

Department of Chemistry, National Taiwan University, Taipei, Taiwan.

出版信息

Electrophoresis. 2007 Nov;28(21):3922-9. doi: 10.1002/elps.200700059.

Abstract

Enantioseparations of five chiral phenothiazines in CD-modified CZE using the single isomer sulfate-substituted beta-CD (heptakis(2,3-dihydroxy-6-O-sulfo)-beta-CD, SI-S-beta-CD) and dual CD systems consisting of SI-S-beta-CD and a neutral CD as chiral selectors in a citrate buffer at pH 3.0 were investigated. The results indicate that SI-S-beta-CD is an excellent chiral selector for enantioseparation of promethazine. The enantiomers of trimeprazine were well separated, while those of ethopropazine could also be baseline-resolved with SI-S-beta-CD. With dual CD systems, especially with hydroxypropyl-beta-CD (HP-beta-CD) as neutral CD, the enantioselectivity of thioridazine and ethopropazine was considerably enhanced. Effective enantioseparation of phenothiazines, except for methotrimeprazine, could thus be favorably and simultaneously achieved. Moreover, reversal of the enantiomer migration order of ethopropazine and thioridazine occurred by varying the concentration of gamma-CD in the presence of SI-S-beta-CD. These phenomena may be attributable to the opposite effects of sulfated beta-CD and gamma-CD on the mobility of the enantiomers of ethopropazine and of thioridazine. Comparative studies on the enantioseparations of phenothiazines with single CD and dual CD systems containing SI-S-beta-CD and randomly sulfate-substituted beta-CD (MI-S-beta-CD) were made.

摘要

研究了在pH 3.0的柠檬酸盐缓冲液中,使用单异构体硫酸根取代的β-环糊精(七(2,3-二羟基-6-O-磺基)-β-环糊精,SI-S-β-CD)以及由SI-S-β-CD和中性环糊精组成的双环糊精体系作为手性选择剂,在CD修饰的毛细管区带电泳中对五种手性吩噻嗪进行对映体拆分。结果表明,SI-S-β-CD是异丙嗪对映体拆分的优良手性选择剂。异丁嗪的对映体得到了很好的分离,而乙丙嗪的对映体也能用SI-S-β-CD实现基线分离。使用双环糊精体系,特别是以羟丙基-β-环糊精(HP-β-CD)作为中性环糊精时,硫利达嗪和乙丙嗪的对映选择性显著提高。因此,可以顺利且同时实现除甲氧异丁嗪外的吩噻嗪的有效对映体拆分。此外,在SI-S-β-CD存在下,通过改变γ-环糊精的浓度,乙丙嗪和硫利达嗪的对映体迁移顺序发生了反转。这些现象可能归因于硫酸化β-环糊精和γ-环糊精对乙丙嗪和硫利达嗪对映体迁移率的相反影响。对吩噻嗪在单环糊精体系以及含有SI-S-β-CD和随机硫酸根取代的β-环糊精(MI-S-β-CD)的双环糊精体系中的对映体拆分进行了比较研究。

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