Workplace chemical
exposures are a major source of occupational
injury. Although over half of these are skin exposures, exposomics
research often focuses on chemical levels in the air or in worker
biofluids such as blood and urine. Until now, one limitation has been
the lack of methods to quantitatively measure surface chemical transfer.
Outside the realm of harmful chemicals, the small molecules we leave
behind on surfaces can also reveal important aspects of human behavior.
In this study, we developed a swab-based quantitative approach to
determine small molecule concentrations across common surfaces. We
demonstrate its utility using one drug, cyclobenzaprine, on metal
surfaces, and two human-derived metabolites, carnitine and phenylacetylglutamine,
on four common surfaces: linoleum flooring, plastified laboratory
workbench, metal, and Plexiglas. We observed peak areas proportional
to surface analyte concentrations at 45 min and 1 week after deposition,
enabling quantification of molecule abundance on workplace built environment
surfaces. In contrast, this method was unsuitable for analysis of
oleanolic acid, for which we did not observe a strong linear proportional
relationship following swab-based recovery from surfaces. Overall,
this method paves the way for future quantitative exposomics studies
in analyte-specific and surface-specific frameworks.