Preparation and evaluation of a vancomycin-immobilized silica monolith as chiral stationary phase for CEC
โ Scribed by Xiaoli Dong; Jing Dong; Junjie Ou; Yan Zhu; Hanfa Zou
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 306 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0173-0835
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
Enantiomeric separations in CEC with the macrocyclic antibiotic vancomycin immobilized silica monolith as a chiral stationary phase are presented. The monolithic silica capillary columns were prepared by a solโgel process in fusedโsilica capillaries with an inner diameter of 50โ ฮผm and subsequently in situ immobilization of vancomycin as a chiral selector by reductive amination. Enantioselectivity was obtained for eight pairs of enantiomers in nonaqueous polar organic or aqueous mobile phases and most of them were baselineโseparated with high column efficiencies. It was observed that the organic modifier ratio (MeOH/ACN) in the polar organic mobile phase played a significant role in controlling the resolution and efficiency of the enantiomers. In enantiomeric separation of propranolol, repeatability for column efficiency and resolution in the nonaqueous mobile phase was given in terms of RSD values at 1.1 and 2.3% (nโ =โ 5) for runโtoโrun injections and 7.2 and 9.6% (nโ =โ 5) for columnโtoโcolumn testing while repeatability for the separation of thalidomide in the aqueous mobile phase was given in terms of RSD values at 1.5, 2.8% and 6.1, 10.5%, respectively.
๐ SIMILAR VOLUMES
Chromatographic silica (10 lm) was chemically modified with the silylating agent: [3-(2-aminoethyl)aminopropyl]trimethoxysilane (AEAPTS). The reaction product was characterized by elemental analysis and infrared and 13 C and 29 Si NMR spectra. The chemically modified silica was treated with Cu(II) i
Two selectors derived from [(S)-1-(1-naphthyl)ethyl]amine and (S)-leucine have been chemically bonded to one another and the resulting chiral auxiliary linked covalently to silica gel, to produce a new chiral stationary phase (CSP) for the HPLC resolution of enantiomers. The CSP is able to separate