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8.

The sensitivities reported in Table 4 are troubling. The sensitivity for As(III) is ~15% lower than

that of MMAs and As(V), and the sensitivity for DMAs is 10% higher than that of MMAs and

As(V). This strongly suggests that there are either impurities in standards (possible) or that the

integrations are not correct (more likely). The sensitivities for all species should be identical, and

this is an important QA measure to control. When this method was published on the FDA

website, there were some chromatogram posted as well, and they showed some As(III) tailing

into the DMAs, and the integration for DMAs was being biased, causing high-bias for DMA.

Based on the sensitivities listed in Table 4, this could be happening with this method.