Analysis of pesticides in nutraceuticals, particularly dietary botanical supplements, is challenging owing to the low water content of powder or tablet samples and potentially higher concentration of co‐extracts produced during the drying and manufacturing processes. These co‐extracts can cause signal suppression or enhancement in mass spectrometric (MS) detection. Poor chromatographic stability and peak shapes can also be observed from co‐eluting matrix components. Sample preparation is critical to the detection of pesticides in extracts, and the major sample preparation methods used for dietary botanical supplements included modified QuEChERS (quick, easy, cheap, effective, rugged, and safe) methods, dilute‐and‐shoot, and pressurized liquid extraction (PLE) with in‐cell (on‐line) cleanup. Additional cleanup of extracts was completed by dispersive solid‐phase extraction (dSPE) or solid‐phase extraction (SPE). Recoveries of individual pesticides from a variety of chemical classes of varying polarities were evaluated using the major sample preparation approaches utilized for analysis of pesticides since 2010. Major chemical classes of pesticides included those predominately analyzed by GC‐MS/MS (pyrethroid insecticides) or LC‐MS/MS (carbamates, sulfonyl ureas, phenyl ureas, and neonicotinoid insecticides) and those that have greater flexibility to be analyzed by GC‐MS/MS or LC‐MS/MS (azole and strobilurin fungicides). Other selected herbicides including cyclohexene oxime herbicides, aryloxyphenoxy propionic herbicides, or fungicides that were included in multiresidue analysis methods were also examined. Common dSPE sorbents included primary secondary amine (PSA), octyldecyl silane (C18), graphitized carbon black (GCB), and zirconia and C18 bonded to silica (Z‐Sep + ), while carbon‐based sorbents were used for SPE along with Florisil ® . C18 and PSA were also used for SPE often in combination with a carbon‐based sorbent. Highlighted are the issues with different chemical classes or sample matrix types.

A liquid chromatography-tandem mass spectrometry method has been developed for the simultaneous determination of metabolites of neonicotinoid insecticides with neonicotinoid insecticides and strobilurin fungicides in the particle phase fraction of atmospheric samples. Pressurized solvent extraction was used to extract the target analytes from particles collected on glass fiber filters, followed by a C18 SPE cleanup step. Recoveries of 85.9 to 108.3% and relative standard deviation <13% were obtained for all analytes. The method detection limit for metabolites of neonicotinoid insecticides were 0.5-3 ng/ mL (air concentrations of 0.44-2.66 pg/m³). Matrix effects were compensated for using standard addition calibration for quantitation. This paper provides the first detection of desmethyl-thiamethoxam which coincided with higher concentrations of thiamethoxam in atmospheric particles. Other neonicotinoid insecticides and strobilurin fungicides detected in the particle phase in the atmosphere included acetamiprid, clothianidin, imidacloprid, azoxystrobin, kresoxim-methyl, pyraclostrobin, and trifloxystrobin. This research highlights the potential of not only neonicotinoid insecticides and strobilurin fungicides moving in the atmosphere in the particle phase, but also a metabolite of thiamethoxam (desmethyl-thiamethoxam) in a region with orchards and vineyards where foliar applications with air blast sprayers dominate.