Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/3654
DC FieldValueLanguage
dc.contributor.authorNagar, Rachana-
dc.contributor.authorSarkar, Dibyendu-
dc.contributor.authorMakris, Konstantinos C.-
dc.contributor.authorDatta, Rupali K.-
dc.contributor.authorSylvia, Victor L.-
dc.date.accessioned2015-03-19T10:57:48Z-
dc.date.accessioned2015-12-08T11:09:37Z-
dc.date.available2015-03-19T10:57:48Z-
dc.date.available2015-12-08T11:09:37Z-
dc.date.issued2009-11-
dc.identifier.citationArchives of Environmental Contamination and Toxicology, 2009, vol. 57, no. 4, pp. 755-766en_US
dc.identifier.issn14320703-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/3654-
dc.description.abstractEarlier incubation and greenhouse studies in our laboratory confirmed the effectiveness of drinking-water treatment residual (WTR) in decreasing soil arsenic (As) bioaccessibility as determined with in vitro tests, which led us to hypothesize a similar outcome if animal studies were to be conducted. Our objective was to evaluate the potential of WTR in lowering soil As bioavailability by conducting in vivo experiments and compare the in vitro to the in vivo As data. This study was performed using 6-week-old male BALB/c mice that were fed with an As-contaminated soil slurry using the gavage method. Blood and stomach contents were collected at 1 and 24 h after feeding. Urine and excreta were collected at time 0 (before feeding) and 24 h after feeding. Relative As bioavailability (RBA) values calculated from the blood samples of mice fed with WTR and WTR-amended soil samples ranged from 13% to 24% and from 25% to 29%, respectively; both were significantly (p < 0.001) lower than that of the unamended (no-WTR) soil (~100% RBA). Absolute As bioavailability (ABA) in the gastric phase was significantly (p < 0.001) lowered, to 7-16%, in the WTR-amended soil compared with that of the unamended control (26%). A significant (p < 0.001) linear correlation (r = 0.94) was observed between the in vitro (stomach-phase) and the in vivo RBA data. Percentage recovery of As obtained from four mice tissue compartments (i.e., blood, stomach, urine, and fecal matter) after oral and intramuscular administrations was 63-80%. Results illustrate the effectiveness of in situ WTR amendment in decreasing in vivo soil As bioavailability, thereby lowering the potential cancer risk via an oral ingestion pathway.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofArchives of Environmental Contamination and Toxicologyen_US
dc.rights© Springer Natureen_US
dc.subjectAluminumen_US
dc.subjectArsenicen_US
dc.subjectIronen_US
dc.subjectWater treatmenten_US
dc.subjectGreenhouse ecosystemen_US
dc.subjectDrinking wateren_US
dc.subjectBioavailabilityen_US
dc.titleBioavailability and bioaccessibility of arsenic in a soil amended with drinking-water treatment residualsen_US
dc.typeArticleen_US
dc.collaborationWeiss Associatesen_US
dc.collaborationMontclair State Universityen_US
dc.collaborationCyprus International Institute for the Environment and Public Healthen_US
dc.collaborationMichigan Technological Universityen_US
dc.collaborationUniversity of Texasen_US
dc.subject.categoryEarth and Related Environmental Sciencesen_US
dc.journalsSubscriptionen_US
dc.reviewPeer Revieweden
dc.countryCyprusen_US
dc.countryUnited Statesen_US
dc.subject.fieldNatural Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1007/s00244-009-9318-7en_US
dc.dept.handle123456789/108en
dc.relation.issue4en_US
dc.relation.volume57en_US
cut.common.academicyear2009-2010en_US
dc.identifier.spage755en_US
dc.identifier.epage766en_US
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.languageiso639-1en-
crisitem.journal.journalissn1432-0703-
crisitem.journal.publisherSpringer Nature-
crisitem.author.deptDepartment of Rehabilitation Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0001-5251-8619-
crisitem.author.parentorgFaculty of Health Sciences-
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