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TITLE:
The development of a pregnancy PBPK Model for Bisphenol A and its evaluation with the available biomonitoring data - imarina:4683528

URV's Author/s:Kumar, Vikas / Schuhmacher Ansuategui, Marta
Author, as appears in the article.:Prasad Sharma, Raju; Schuhmacher, Marta; Kumar, Vikas
Author's mail:vikas.kumar@urv.cat
marta.schuhmacher@urv.cat
Author identifier:0000-0002-9795-5967
0000-0003-4381-2490
Journal publication year:2018
Publication Type:Journal Publications
APA:Prasad Sharma, Raju; Schuhmacher, Marta; Kumar, Vikas (2018). The development of a pregnancy PBPK Model for Bisphenol A and its evaluation with the available biomonitoring data. Science Of The Total Environment, 624(), 55-68. DOI: 10.1016/j.scitotenv.2017.12.023
Paper original source:Science Of The Total Environment. 624 55-68
Abstract:Recent studies suggest universal fetal exposure to Bisphenol A (BPA) and its association with the adverse birth outcomes. Estimation of the fetal plasma BPA concentration from the maternal plasma BPA would be highly useful to predict its associated risk to this specific population. The objective of current work is to develop a pregnancy-physiologically based pharmacokinetic (P-PBPK) model to predict the toxicokinetic profile of BPA in the fetus during gestational growth, and to evaluate the developed model using biomonitoring data obtained from different pregnancy cohort studies. To achieve this objective, first, the adult PBPK model was developed and validated with the human BPA toxicokinetic data. This validated human PBPK model was extended to develop a P-PBPK model, which included the physiological changes during pregnancy and the fetus sub-model. The developed model would be able to predict the BPA pharmacokinetics (PKs) in both mother and fetus. Transplacental BPA kinetics parameters for this study were taken from the previous pregnant mice study. Both oral and dermal exposure routes were included into the model to simulate total BPA internal exposure. The impact of conjugation and deconjugation of the BPA and its metabolites on fetal PKs was investigated. The developed P-PBPK model was evaluated against the observed BPA concentrations in cord blood, fetus liver and amniotic fluid considering maternal blood concentration as an exposure source. A range of maternal exposure dose for the oral and dermal routes was estimated, so that simulation concentration matched the observed highest and lowest mother plasma concentration in different cohorts' studies. The developed model could be used to address the concerns regarding possible adverse health effects in the fetus being exposed to BPA and might be useful in identifying critical windows of exposure during pregnancy.
Article's DOI:10.1016/j.scitotenv.2017.12.023
Link to the original source:https://www.sciencedirect.com/science/article/abs/pii/S0048969717334423
Paper version:info:eu-repo/semantics/acceptedVersion
licence for use:https://creativecommons.org/licenses/by/3.0/es/
Department:Enginyeria Química
Licence document URL:https://repositori.urv.cat/ca/proteccio-de-dades/
Thematic Areas:Zootecnia / recursos pesqueiros
Waste management and disposal
Saúde coletiva
Química
Pollution
Odontología
Nutrição
Medicina veterinaria
Medicina iii
Medicina ii
Medicina i
Materiais
Matemática / probabilidade e estatística
Interdisciplinar
Historia
Geografía
Geociências
Farmacia
Environmental sciences
Environmental engineering
Environmental chemistry
Ensino
Engenharias iii
Engenharias ii
Engenharias i
Enfermagem
Direito
Ciências biológicas iii
Ciências biológicas ii
Ciências biológicas i
Ciências ambientais
Ciências agrárias i
Ciência de alimentos
Ciência da computação
Biotecnología
Biodiversidade
Astronomia / física
Keywords:Window of exposure
Pregnancy-pbpk
Pregnancy
Phenols
Models, biological
Mice
Maternal exposure
Humans
Fetal exposure
Female
Environmental monitoring
Bisphenol a
Biomonitoring
Benzhydryl compounds
Animals
pregnancy-pbpk
fetal exposure
bisphenol a
biomonitoring
Entity:Universitat Rovira i Virgili
Record's date:2025-02-08
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