Source:http://linkedlifedata.com/resource/pubmed/id/21298667
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3-4
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pubmed:dateCreated |
2011-2-7
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pubmed:abstractText |
Nanoparticles exhibiting favorable surface-to-volume ratios create efficient stationary phases for electrochromatography. New nanomaterials derived from chitosan (CS) were immobilized onto modified capillaries for use as the chiral stationary phase (CSP) in open-tubular electrochromatography. This immobilization was achieved through the copolymerization of glycidyl methacrylate-modified nano-CS with methacrylamide (MAA) and bis-acrylamide crosslinkers (forming the MAA-CS capillary) rather than the attachment of nano-CS to the copolymer of glycidyl methacrylate, MAA, and bis-acrylamide (forming the MAA+CS capillary). The completed MAA-CS capillary and its precursors were examined by SEM and ATR-IR measurements. Before separating chiral samples, the MAA-CS capillary was characterized by electroosmotic flow measurements at varying pH values, concentrations, and volume percentages of organic modifiers in the running buffers. Tryptophan enantiomers were well separated by the MAA-CS capillary, whereas no enantioselectivity was observed in the MAA+CS capillary. With the addition of 80% MeOH into the phosphate buffer, the chiral separation of (±)-catechin was accomplished in a normal-phase mode. However, the new CSP has its limitations, as only two groups of ?-tocopherol stereoisomers were separated.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acrylamides,
http://linkedlifedata.com/resource/pubmed/chemical/Acrylic Resins,
http://linkedlifedata.com/resource/pubmed/chemical/Catechin,
http://linkedlifedata.com/resource/pubmed/chemical/Chitosan,
http://linkedlifedata.com/resource/pubmed/chemical/Tryptophan,
http://linkedlifedata.com/resource/pubmed/chemical/alpha-Tocopherol,
http://linkedlifedata.com/resource/pubmed/chemical/methacrylamide,
http://linkedlifedata.com/resource/pubmed/chemical/polyacrylamide
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1522-2683
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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pubmed:issnType |
Electronic
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pubmed:volume |
32
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
398-407
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pubmed:meshHeading |
pubmed-meshheading:21298667-Acrylamides,
pubmed-meshheading:21298667-Acrylic Resins,
pubmed-meshheading:21298667-Capillary Electrochromatography,
pubmed-meshheading:21298667-Catechin,
pubmed-meshheading:21298667-Chitosan,
pubmed-meshheading:21298667-Electroosmosis,
pubmed-meshheading:21298667-Microscopy, Electron, Scanning,
pubmed-meshheading:21298667-Nanoparticles,
pubmed-meshheading:21298667-Nanotechnology,
pubmed-meshheading:21298667-Tryptophan,
pubmed-meshheading:21298667-alpha-Tocopherol
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pubmed:year |
2011
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pubmed:articleTitle |
Nanochitosan crosslinked with polyacrylamide as the chiral stationary phase for open-tubular capillary electrochromatography.
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pubmed:affiliation |
School of Pharmacy, China Medical University, Taichung, Taiwan. cjl@mail.cmu.edu.tw
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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