TY - JOUR
T1 - Using soil properties to predict in vivo bioavailability of lead in soils
AU - Wijayawardena, M. A.Ayanka
AU - Naidu, Ravi
AU - Megharaj, Mallavarapu
AU - Lamb, Dane
AU - Thavamani, Palanisami
AU - Kuchel, Tim
N1 - Funding Information:
In vivo swine bioavailability study was funded through a CRC CARE postgraduate scholarship and laboratory facilities were provided by CERAR, UniSA. Swine studies were approved and conducted according to application number 39a/12 of the SA Pathology Animal Ethics Committee. The authors would like to acknowledge the Centre of Environmental Risk Assessment and Remediation (University of South Australia) and South Australian Health and Medical Research Institute (SAHMRI) for this research. Authors would also like to thank C. Danidu Kudagamage for his assistance with the sorption experiments and soil characterization, Ray Correll for statistical support.
Publisher Copyright:
© 2015 Elsevier Ltd.
PY - 2015/11/1
Y1 - 2015/11/1
N2 - Soil plays a significant role in controlling the potential bioavailability of contaminants in the environment. In this study, eleven soils were used to investigate the relationship between soil properties and relative bioavailability (RB) of lead (Pb). To minimise the effect of source of Pb on in vivo bioavailability, uncontaminated study soils were spiked with 1500mg Pb/kg soil and aged for 10-12months prior to investigating the relationships between soil properties and in vivo RB of Pb using swine model. The biological responses to oral administration of Pb in aqueous phase or as spiked soils were compared by applying a two-compartment pharmacokinetic model to blood Pb concentration. The study revealed that RB of Pb from aged soils ranged from 30±9% to 83±7%. The very different RB of Pb in these soils was attributed to variations in the soils' physico-chemical properties. This was established using sorption studies showing: firstly, Freundlich partition coefficients that ranged from 21 to 234; and secondly, a strongly significant (R2=0.94, P<0.001) exponential relationship between RB and Freundlich partition coefficient (Kd). This simple exponential model can be used to predict relative bioavailability of Pb in contaminated soils. To the best of our knowledge, this is the first such model derived using sorption partition coefficient to predict the relative bioavailability of Pb.
AB - Soil plays a significant role in controlling the potential bioavailability of contaminants in the environment. In this study, eleven soils were used to investigate the relationship between soil properties and relative bioavailability (RB) of lead (Pb). To minimise the effect of source of Pb on in vivo bioavailability, uncontaminated study soils were spiked with 1500mg Pb/kg soil and aged for 10-12months prior to investigating the relationships between soil properties and in vivo RB of Pb using swine model. The biological responses to oral administration of Pb in aqueous phase or as spiked soils were compared by applying a two-compartment pharmacokinetic model to blood Pb concentration. The study revealed that RB of Pb from aged soils ranged from 30±9% to 83±7%. The very different RB of Pb in these soils was attributed to variations in the soils' physico-chemical properties. This was established using sorption studies showing: firstly, Freundlich partition coefficients that ranged from 21 to 234; and secondly, a strongly significant (R2=0.94, P<0.001) exponential relationship between RB and Freundlich partition coefficient (Kd). This simple exponential model can be used to predict relative bioavailability of Pb in contaminated soils. To the best of our knowledge, this is the first such model derived using sorption partition coefficient to predict the relative bioavailability of Pb.
KW - In vivo
KW - Relative bioavailability
KW - Soil properties
KW - Sorption
KW - Swine
UR - http://www.scopus.com/inward/record.url?scp=84940936043&partnerID=8YFLogxK
U2 - 10.1016/j.chemosphere.2015.06.073
DO - 10.1016/j.chemosphere.2015.06.073
M3 - Article
C2 - 26151314
AN - SCOPUS:84940936043
SN - 0045-6535
VL - 138
SP - 422
EP - 428
JO - Chemosphere
JF - Chemosphere
ER -