Physiologically Based Pharmacokinetic Modeling of Salivary Concentrations for Noninvasive Biomonitoring of 2, 4-Dichlorophenoxyacetic Acid (2, 4-D). (21st September 2019)

• Record Type: Journal Article
• Authors: Han, Alice A; Timchalk, Charles; Carver, Zana A; Weber, Thomas J; Tyrrell, Kimberly J; Sontag, Ryan L; Gibbins, Teresa; Chrisler, William B; Weitz, Karl K; Du, Dan; Lin, Yuehe; Smith, Jordan N
• Is Part Of: Toxicological sciences. Volume 172:Number 2(2019)
• Page Start: 330
• Page End: 343
• Publication Date: 2019-09-21
• Subjects: salivary biomonitoring -- 2, 4-dichlorophenoxyacetic acid -- PBPK modeling; Toxicology -- Periodicals; Toxicology -- Periodicals; Toxicology; Periodicals; 615.9
• DOI: 10.1093/toxsci/kfz206
• Languages: English
• ISSNs: 1096-6080

Abstract

Abstract: Saliva has become a favorable sample matrix for biomonitoring due to its noninvasive attributes and overall flexibility in collection. To ensure measured salivary concentrations reflect the exposure, a solid understanding of the salivary transport mechanism and relationships between salivary concentrations and other monitored matrices (ie, blood, urine) is needed. Salivary transport of a commonly applied herbicide, 2, 4-dichlorophenoxyacetic acid (2, 4-D), was observed in vitro and in vivo and a physiologically based pharmacokinetic (PBPK) model was developed to translate observations from the cell culture model to those in animal models and further evaluate 2, 4-D kinetics in humans. Although apparent differences in experimental in vitro and in vivo saliva:plasma ratios (0.034 and 0.0079) were observed, simulations with the PBPK model demonstrated dynamic time and dose-dependent saliva:plasma ratios, elucidating key mechanisms affecting salivary transport. The model suggested that 2, 4-D exhibited diffusion-limited transport to saliva and was additionally impacted by protein binding saturation and permeability across the salivary gland. Consideration of sampling times post-exposure and potential saturation of transport mechanisms are then critical aspects for interpreting salivary 2, 4-D biomonitoring observations. This work utilized PBPK modeling in in vitro to in vivo translation to explore benefits and limitations of salivary analysis for occupational biomonitoring.