Environ Health Toxicol.  2014 ;29(1):e2014018. 10.5620/eht.e2014018.

The separation of arsenic metabolites in urine by high performance liquid chromatographyinductively coupled plasma-mass spectrometry

Affiliations
  • 1Heavy Metal Exposure Environmental Health Center, Dong-A University, Busan, Korea. yshong@dau.ac.kr
  • 2Agilent Technologies Korea Ltd., Seoul, Korea.
  • 3Department of Dermatology, Dong-A University Hospital, Busan, Korea.
  • 4Department of Preventive Medicine, Dong-A University College of Medicine, Busan, Korea.

Abstract


OBJECTIVES
The purpose of this study was to determine a separation method for each arsenic metabolite in urine by using a high performance liquid chromatography (HPLC)- inductively coupled plasma-mass spectrometer (ICP-MS).
METHODS
Separation of the arsenic metabolites was conducted in urine by using a polymeric anion-exchange (Hamilton PRP X-100, 4.6 mm x 150 mm, 5 mum) column on Agilent Technologies 1260 Infinity LC system coupled to Agilent Technologies 7700 series ICP/MS equipment using argon as the plasma gas.
RESULTS
All five important arsenic metabolites in urine were separated within 16 minutes in the order of arsenobetaine, arsenite, dimethylarsinate, monomethylarsonate and arsenate with detection limits ranging from 0.15 to 0.27 mug/L (40 muL injection). We used GEQUAS No. 52, the German external quality assessment scheme and standard reference material 2669, National Institute of Standard and Technology, to validate our analyses.
CONCLUSIONS
The method for separation of arsenic metabolites in urine was established by using HPLC-ICP-MS. This method contributes to the evaluation of arsenic exposure, health effect assessment and other bio-monitoring studies for arsenic exposure in South Korea.

Keyword

Arsenic; Arsenic metabolites; HPLC-ICP-MS; Urine

MeSH Terms

Argon
Arsenic*
Cacodylic Acid
Chromatography, Liquid
Environmental Monitoring
Korea
Limit of Detection
Plasma
Polymers
Spectrum Analysis*
Argon
Arsenic
Cacodylic Acid
Polymers
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