Source:http://linkedlifedata.com/resource/pubmed/id/20506424
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
13
|
pubmed:dateCreated |
2010-7-5
|
pubmed:abstractText |
A simple and rapid CZE method was established for the simultaneous determination of valienamine, acarbose and validamycin A, using a 20-kV CZE with the detection wavelength of 193 nm and 50 mM phosphoric acid-20 mM Tris (pH 5.3) as a running buffer. The calibration curves of valienamine, acarbose, and validamycin A showed a good linear relationship at a concentration range of 5-1000 microg/mL. The detection limits of valienamine, acarbose, and validamycin A were 0.3, 0.6, and 0.6 microg/mL, respectively, and the average recoveries of each of the above were 99.9, 99.5, and 100.3%. The method has been successfully applied for simultaneous determination of substrate and product in the process of preparation of valienamine.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acarbose,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclohexenes,
http://linkedlifedata.com/resource/pubmed/chemical/Hexosamines,
http://linkedlifedata.com/resource/pubmed/chemical/Inositol,
http://linkedlifedata.com/resource/pubmed/chemical/validamycin A,
http://linkedlifedata.com/resource/pubmed/chemical/valienamine
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
1615-9314
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
33
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1997-2001
|
pubmed:meshHeading | |
pubmed:year |
2010
|
pubmed:articleTitle |
Simultaneous determination of substrate and product in the process of preparation of valienamine by capillary zone electrophoresis.
|
pubmed:affiliation |
Shanghai Institute of Pharmaceutical Industry, Shanghai, P. R. China. weixdong@hotmail.com
|
pubmed:publicationType |
Journal Article
|