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Electrophoresis ; 31(10): 1697-705, 2010 May.
Article in English | MEDLINE | ID: mdl-20401901

ABSTRACT

The application of chemical-modified gold nanoparticles (GNPs) as chiral selector for the enantioseparation based on pseudostationary phase-CEC (PSP-CEC) is presented. GNPs modified by thiolated beta-CD were characterized by NMR and FT-IR. The nanoparticle size was determined to be of 9.5 nm (+2.5 nm) by Transmission Electron Microscopy (TEM) and UV spectra. Four pairs of dinitrophenyl-labeled amino acid enantiomers (DL-Val, Leu, Glu and Asp) and three pairs of drug enantiomers (RS-chlorpheniramine, zopiclone and carvedilol) were analyzed by using modified GNPs as the chiral selector in PSP-CEC. Good theoretical plate number (up to 2.4x10(5) per meter) and separation resolution (up to 4.7) were obtained even with low concentration of modified GNPs (0.8-1.4 mg/mL). The corresponding concentration of beta-CD in the buffer was only 0.30-0.53 mM, which was much lower than the optimum concentration of 15 mM if pure beta-CD was used as chiral selector. Our results showed that thiolated beta-CD modified GNPs have more sufficient interaction with the analytes, resulting in significant enhancement of enantioseparation. The study shed light on potential usage of chemical modified GNPs as chiral selector for enantioseparation based on PSP-CEC.


Subject(s)
Amino Acids/isolation & purification , Capillary Electrochromatography/methods , Cyclodextrins/chemistry , Gold/chemistry , Metal Nanoparticles/chemistry , Pharmaceutical Preparations/isolation & purification , Amino Acids/chemistry , Azabicyclo Compounds/chemistry , Azabicyclo Compounds/isolation & purification , Carbazoles/chemistry , Carbazoles/isolation & purification , Carvedilol , Chlorpheniramine/chemistry , Chlorpheniramine/isolation & purification , Microscopy, Electron, Transmission , Pharmaceutical Preparations/chemistry , Piperazines/chemistry , Piperazines/isolation & purification , Propanolamines/chemistry , Propanolamines/isolation & purification , Stereoisomerism , Sulfhydryl Compounds/chemistry
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