TY - JOUR
T1 - Speciation of dimethylarsinyl-riboside derivatives (arsenosugars) in marine reference materials by HPLC-ICP-MS
AU - Larsen, Erik Huusfeldt
PY - 1995
Y1 - 1995
N2 - Anion and cation exchange HPLC-ICP-MS was used to separate and detect mixtures of four dimethylarsinyl-riboside derivatives (arsenosugars), in the presence of eight other arsenic species naturally occurring in the marine environment. The separations achieved showed that two arsenosugars 11 and 13 (cf. Table 2) were present in shellfish certified reference materials (CRMs) and in a lobster hepatopancreas CRM. The concentration of the two arsenosugars in the shellfish samples amounts to 18% of the total arsenic as compared to arsenobetaine at 9–13% and dimethylarsinate at 4–9% of the total arsenic. Additionally, a chromatographic peak with the same retention time as that of 2-dimethylarsinylacetic acid was detected in the shellfish samples. Further support of the identity of this peak was gained after spiking the sample extracts with the standard substance which resulted in a single, but larger peak. The indication that this novel arsenical is present in shellfish, and the recently reported finding of arsenocholine in seafood supports a proposed marine biosynthetic pathway of arsenic that includes both of these compounds as the immediate precursors of arsenobetaine, the end-product of the marine arsenic metabolism.
AB - Anion and cation exchange HPLC-ICP-MS was used to separate and detect mixtures of four dimethylarsinyl-riboside derivatives (arsenosugars), in the presence of eight other arsenic species naturally occurring in the marine environment. The separations achieved showed that two arsenosugars 11 and 13 (cf. Table 2) were present in shellfish certified reference materials (CRMs) and in a lobster hepatopancreas CRM. The concentration of the two arsenosugars in the shellfish samples amounts to 18% of the total arsenic as compared to arsenobetaine at 9–13% and dimethylarsinate at 4–9% of the total arsenic. Additionally, a chromatographic peak with the same retention time as that of 2-dimethylarsinylacetic acid was detected in the shellfish samples. Further support of the identity of this peak was gained after spiking the sample extracts with the standard substance which resulted in a single, but larger peak. The indication that this novel arsenical is present in shellfish, and the recently reported finding of arsenocholine in seafood supports a proposed marine biosynthetic pathway of arsenic that includes both of these compounds as the immediate precursors of arsenobetaine, the end-product of the marine arsenic metabolism.
U2 - 10.1007/BF00323078
DO - 10.1007/BF00323078
M3 - Journal article
SN - 0937-0633
VL - 352
SP - 582
EP - 588
JO - Fresenius Journal of Analytical Chemistry
JF - Fresenius Journal of Analytical Chemistry
IS - 6
ER -