Quantitative analysis of valiolamine through pre-column derivatization with phenylisocyanate using high-performance liquid chromatography with UV detection: Selection of reagent, identification of derivative and optimization of derivatization conditions

Li, He; Lee, J; Nguyen, D; Kim, S; Seo, Y; Chang, YK; Hong, SK; Moon, M; Chung, InY; Kim, CJ

HERO ID

2030140

Reference Type

Journal Article

Year

2009

Language

English

PMID

19303235

HERO ID 2030140
In Press No
Year 2009
Title Quantitative analysis of valiolamine through pre-column derivatization with phenylisocyanate using high-performance liquid chromatography with UV detection: Selection of reagent, identification of derivative and optimization of derivatization conditions
Authors Li, He; Lee, J; Nguyen, D; Kim, S; Seo, Y; Chang, YK; Hong, SK; Moon, M; Chung, InY; Kim, CJ
Journal Journal of Pharmaceutical and Biomedical Analysis
Volume 49
Issue 4
Page Numbers 957-963
Abstract This report describes the improved quantitative determination of valiolamine in a medium for microbial culture using high-performance liquid chromatography with UV detection. Valiolamine aqueous solution was dried, dissolved in dimethyl sulfoxide and derivatization performances of phenylisocyanate (PHI), 1-fluoro-2,4-dinitrobenznene and 1-naphthylisothiocyanate were compared in the presence of triethylamine. The PHI was chosen as the most suitable derivatization reagent and the valiolamine-PHI derivative was identified by thin-layer chromatography and electrospray ionization mass spectrometry. The derivative eluted at 10.5 min on a reverse-phase column using a mobile phase composed of 10% acetonitrile in water containing 0.5 mM sodium octyl sulfate (pH 3.0), at a column flow rate of 1.0 mL/min with UV detection at 240 nm. The optimum conditions for derivatization were a reaction temperature of 30 degrees C, reaction time of 30 min, and PHI concentration higher than 33.6 mM. Calibration curves were linear in the range of 0.99-19.95 microg/mL for the standard solutions and 24.9-99.7 microg/mL for the spiked sample. The proposed method was validated and proven to be selective, accurate and precise and suitable for the quantitative analysis of valiolamine in medium for microbial cultures.
Doi 10.1016/j.jpba.2009.02.020
Pmid 19303235
Wosid WOS:000265046200013
Is Certified Translation No
Dupe Override No
Comments Scopus URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-62949164447&doi=10.1016%2fj.jpba.2009.02.020&partnerID=40&md5=b28e4d94c3089557528a2f23cec317d0
Is Public Yes
Language Text English
Keyword Valiolamine; Phenylisocyanate; Derivatization; HPLC; UV detection