Speciation of arsenic compounds by using ion-pair chromatography with atomic spectrometry and mass spectrometry detection

被引:71
作者
Le, XC
Ma, MS
机构
[1] Environmental Health Program, Department of Public Health Sciences, University of Alberta, Edmonton
基金
加拿大自然科学与工程研究理事会;
关键词
ion-pairing reagents; detection; LC; arsenic compounds;
D O I
10.1016/S0021-9673(96)00881-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chromatography separation of arsenic compounds is important for chemical speciation studies; yet a complete separation of several biologically and environmentally important arsenic compounds has been difficult to achieve on a single column. We report here baseline resolution for arsenate, arsenite, monomethylarsonic acid, dimethylarsinic acid, arsenobetaine, arsenocholine, and tetramethylarsonium ion, by using mixed ion-pair reagents containing 10 mM hexanesulfonate and 1 mM tetraethylammonium hydroxide, as mobile phase. The complete separation of these anionic, cationic and neutral arsenic species on a reversed-phase C-18 column took only 12 min. Inductively coupled plasma mass spectrometry, hydride generation atomic absorption spectrometry and atomic fluorescence spectrometry systems were used for element-specific detection. The speciation technique was successfully applied to studies of urinary excretion of arsenic compounds following one-time ingestion of shrimp. Arsenobetaine ingested from the consumption of shrimp was excreted into urine in its original form; and approximately 70% of the total arsenobetaine ingested was excreted into urine within 37 h after ingestion.
引用
收藏
页码:55 / 64
页数:10
相关论文
共 56 条
[1]  
Agency for Toxic Substances and Disease Registry, 1993, TOX PROF ARS
[2]  
Andreae M. O., 1986, ORGANOMETALLIC COMPO, P198
[3]   DISTRIBUTION AND SPECIATION OF ARSENIC IN NATURAL-WATERS AND SOME MARINE-ALGAE [J].
ANDREAE, MO .
DEEP-SEA RESEARCH, 1978, 25 (04) :391-402
[4]  
[Anonymous], 1989, TRACE ELEMENT SPECIA
[5]   AUTOMATED PROCEDURE FOR THE DETERMINATION OF SOLUBLE ARSENIC USING HYDRIDE GENERATION ATOMIC-ABSORPTION SPECTROSCOPY [J].
ARBABZAVAR, MH ;
HOWARD, AG .
ANALYST, 1980, 105 (1253) :744-750
[6]  
ARCHARI R, 1983, J CHROMATOGR SCI, V21, P278
[7]   DETERMINATION OF ARSENIC SPECIES BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY - INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRY [J].
BEAUCHEMIN, D ;
SIU, KWM ;
MCLAREN, JW ;
BERMAN, SS .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1989, 4 (03) :285-289
[8]   SEPARATION AND DETERMINATION OF NANOGRAM AMOUNTS OF INORGANIC ARSENIC AND METHYLARSENIC COMPOUNDS [J].
BRAMAN, RS ;
JOHNSON, DL ;
FOREBACK, CC ;
AMMONS, JM ;
BRICKER, JL .
ANALYTICAL CHEMISTRY, 1977, 49 (04) :621-625
[9]   METHYLATED FORMS OF ARSENIC IN ENVIRONMENT [J].
BRAMAN, RS ;
FOREBACK, CC .
SCIENCE, 1973, 182 (4118) :1247-1249
[10]   DETERMINATION OF ARSENIC SPECIES IN FISH BY DIRECTLY COUPLED HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY-INDUCTIVELY COUPLED PLASMA-MASS SPECTROMETRY [J].
BRANCH, S ;
EBDON, L ;
ONEILL, P .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1994, 9 (01) :33-37