“…GC, paired to electron ionization (EI), captures relatively nonpolar (more bioaccumulative), volatile/semivolatile, and thermostable substances, including many hydrophobic organic chemicals (HOCs) like polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), phthalates, and VOCs . With versatile derivatizations, GC-MS has proved effective not only in metabolomics of primary metabolites including sugar, fatty acids, and amino acids, , but in targeting certain exogenous chemicals as well, such as UV-filters (additives in PPCPs) including benzophenone, pharmaceuticals, parabens, and phenols (e.g., bisphenols, alkyl- and halogenated phenols). , LC, coupled to electrospray ionization (ESI), widely applies to nonvolatile, relatively polar/hydrophilic, and thermally unstable chemicals, e.g., pesticides, prescription and illicit drugs, and mycotoxins. , LC-MS is noted for its speed, precision, and capability in the unequivocal detection of trace molecules in vivo , as demonstrated by the screening of doping or illicit drug use in equine or human athletics. , Most LC applications are based on reverse-phase LC (e.g., C 18 and C 8 ). However, there are emerging alternatives like pentafluorophenyl (PFP) stationary phases and hydrophilic interaction chromatography (HILIC) for better retention of relatively polar species or unique isomeric selectivity .…”