Synergistic cytotoxicity of bromoacetic acid and three emerging bromophenolic disinfection byproducts against human intestinal and neuronal cells

Halogenated disinfection byproducts (halo-DBPs) are drinking water contaminants of great public health concern. Nine haloaliphatic DBPs have been regulated by the U.S. Environmental Protection Agency and various halophenolic compounds have been identified as emerging DBPs. In this study, we evaluate...

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Veröffentlicht in:Chemosphere (Oxford) 2022-01, Vol.287, p.131794-131794, Article 131794
Hauptverfasser: Liu, Jiaqi, Gibb, Matthew, Pradhan, Sahar H., Sayes, Christie M.
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Sayes, Christie M.
description Halogenated disinfection byproducts (halo-DBPs) are drinking water contaminants of great public health concern. Nine haloaliphatic DBPs have been regulated by the U.S. Environmental Protection Agency and various halophenolic compounds have been identified as emerging DBPs. In this study, we evaluated the cytotoxic interactions of the regulated bromoacetic acid and three emerging bromophenolic DBPs, i.e., 2,4,6-tribromophenol, 3,5-dibromo-4-hydroxybenzoic acid, and 3,5-dibromo-4-hydroxybenzaldehyde. Cytotoxicity was measured for each DBP individually as well as each of their mixtures using in vitro human epithelial colorectal adenocarcinoma (Caco-2) and neuroblastoma (SH-SY5Y) cells. Concentration addition (CA) model and isobolographic analysis were employed to characterize the interactions among the DBPs. Our results show that the cytotoxicity of four bromo-DBPs against both cell-types followed the descending rank order of bromoacetic acid > 2,4,6-tribromophenol > 3,5-dibromo-4-hydroxybenzaldehyde > 3,5-dibromo-4-hydroxybenzoic acid. Compared with the toxicity data in literature, our finding that bromoacetic acid showed higher cytotoxicity than bromophenolic DBPs was consistent with the results from Chinese hamster ovary cells (a commonly used in vitro model of DBP toxicological studies); but different from the results obtained from in vivo biological models. Significantly, with CA model prediction, we found that mixtures of four bromo-DBPs exhibited synergistic cytotoxic effects on both human cell types. Isobolographic analysis of binary DBP mixtures revealed that, for Caco-2 cells, bromoacetic acid, 2,4,6-tribromophenol, and 3,5-dibromo-4-hydroxybenzoic acid induced synergism; for SH-SY5Y cells, bromoacetic acid induced synergism with all three bromophenolic DBPs. The production of reactive oxidative species (ROS) induced by DBP mixtures could be an important reason for the synergistic cytotoxicity. [Display omitted] •Bromoacetic acid was more cytotoxic than three bromophenolic DBPs against human cells.•Measured LC50 values of mixtures of the four DBPs were lower than predicted by CA model.•Isobolographic analysis was newly employed to characterize interactions of DBP binary mixtures.•Bromoacetic acid exhibited different degrees of synergistic effects with bromophenolic DBPs.•Production of ROS could be an important reason for the synergism of bromo-DBP mixtures.
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Nine haloaliphatic DBPs have been regulated by the U.S. Environmental Protection Agency and various halophenolic compounds have been identified as emerging DBPs. In this study, we evaluated the cytotoxic interactions of the regulated bromoacetic acid and three emerging bromophenolic DBPs, i.e., 2,4,6-tribromophenol, 3,5-dibromo-4-hydroxybenzoic acid, and 3,5-dibromo-4-hydroxybenzaldehyde. Cytotoxicity was measured for each DBP individually as well as each of their mixtures using in vitro human epithelial colorectal adenocarcinoma (Caco-2) and neuroblastoma (SH-SY5Y) cells. Concentration addition (CA) model and isobolographic analysis were employed to characterize the interactions among the DBPs. Our results show that the cytotoxicity of four bromo-DBPs against both cell-types followed the descending rank order of bromoacetic acid &gt; 2,4,6-tribromophenol &gt; 3,5-dibromo-4-hydroxybenzaldehyde &gt; 3,5-dibromo-4-hydroxybenzoic acid. Compared with the toxicity data in literature, our finding that bromoacetic acid showed higher cytotoxicity than bromophenolic DBPs was consistent with the results from Chinese hamster ovary cells (a commonly used in vitro model of DBP toxicological studies); but different from the results obtained from in vivo biological models. Significantly, with CA model prediction, we found that mixtures of four bromo-DBPs exhibited synergistic cytotoxic effects on both human cell types. Isobolographic analysis of binary DBP mixtures revealed that, for Caco-2 cells, bromoacetic acid, 2,4,6-tribromophenol, and 3,5-dibromo-4-hydroxybenzoic acid induced synergism; for SH-SY5Y cells, bromoacetic acid induced synergism with all three bromophenolic DBPs. The production of reactive oxidative species (ROS) induced by DBP mixtures could be an important reason for the synergistic cytotoxicity. [Display omitted] •Bromoacetic acid was more cytotoxic than three bromophenolic DBPs against human cells.•Measured LC50 values of mixtures of the four DBPs were lower than predicted by CA model.•Isobolographic analysis was newly employed to characterize interactions of DBP binary mixtures.•Bromoacetic acid exhibited different degrees of synergistic effects with bromophenolic DBPs.•Production of ROS could be an important reason for the synergism of bromo-DBP mixtures.</description><identifier>ISSN: 0045-6535</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2021.131794</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Cytotoxicity ; DBP ; Disinfection byproduct ; Interaction ; ROS ; Synergism</subject><ispartof>Chemosphere (Oxford), 2022-01, Vol.287, p.131794-131794, Article 131794</ispartof><rights>2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c354t-57cd00e37e195530b8c7c280fb4a58b0897ce17dc0d81428305b4e42f58609163</citedby><cites>FETCH-LOGICAL-c354t-57cd00e37e195530b8c7c280fb4a58b0897ce17dc0d81428305b4e42f58609163</cites><orcidid>0000-0002-9997-992X ; 0000-0002-5529-4101</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0045653521022669$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Liu, Jiaqi</creatorcontrib><creatorcontrib>Gibb, Matthew</creatorcontrib><creatorcontrib>Pradhan, Sahar H.</creatorcontrib><creatorcontrib>Sayes, Christie M.</creatorcontrib><title>Synergistic cytotoxicity of bromoacetic acid and three emerging bromophenolic disinfection byproducts against human intestinal and neuronal cells</title><title>Chemosphere (Oxford)</title><description>Halogenated disinfection byproducts (halo-DBPs) are drinking water contaminants of great public health concern. Nine haloaliphatic DBPs have been regulated by the U.S. Environmental Protection Agency and various halophenolic compounds have been identified as emerging DBPs. In this study, we evaluated the cytotoxic interactions of the regulated bromoacetic acid and three emerging bromophenolic DBPs, i.e., 2,4,6-tribromophenol, 3,5-dibromo-4-hydroxybenzoic acid, and 3,5-dibromo-4-hydroxybenzaldehyde. Cytotoxicity was measured for each DBP individually as well as each of their mixtures using in vitro human epithelial colorectal adenocarcinoma (Caco-2) and neuroblastoma (SH-SY5Y) cells. Concentration addition (CA) model and isobolographic analysis were employed to characterize the interactions among the DBPs. Our results show that the cytotoxicity of four bromo-DBPs against both cell-types followed the descending rank order of bromoacetic acid &gt; 2,4,6-tribromophenol &gt; 3,5-dibromo-4-hydroxybenzaldehyde &gt; 3,5-dibromo-4-hydroxybenzoic acid. Compared with the toxicity data in literature, our finding that bromoacetic acid showed higher cytotoxicity than bromophenolic DBPs was consistent with the results from Chinese hamster ovary cells (a commonly used in vitro model of DBP toxicological studies); but different from the results obtained from in vivo biological models. Significantly, with CA model prediction, we found that mixtures of four bromo-DBPs exhibited synergistic cytotoxic effects on both human cell types. Isobolographic analysis of binary DBP mixtures revealed that, for Caco-2 cells, bromoacetic acid, 2,4,6-tribromophenol, and 3,5-dibromo-4-hydroxybenzoic acid induced synergism; for SH-SY5Y cells, bromoacetic acid induced synergism with all three bromophenolic DBPs. The production of reactive oxidative species (ROS) induced by DBP mixtures could be an important reason for the synergistic cytotoxicity. [Display omitted] •Bromoacetic acid was more cytotoxic than three bromophenolic DBPs against human cells.•Measured LC50 values of mixtures of the four DBPs were lower than predicted by CA model.•Isobolographic analysis was newly employed to characterize interactions of DBP binary mixtures.•Bromoacetic acid exhibited different degrees of synergistic effects with bromophenolic DBPs.•Production of ROS could be an important reason for the synergism of bromo-DBP mixtures.</description><subject>Cytotoxicity</subject><subject>DBP</subject><subject>Disinfection byproduct</subject><subject>Interaction</subject><subject>ROS</subject><subject>Synergism</subject><issn>0045-6535</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqNUUHP1CAQJUYT19X_gDcvXaGUlh7NRv1MvsSDeiZ0mO6yaWEFauzP8B9LrQePXmYy4b03j3mEvObsxBlv395OcMU5pPsVI55qVvMTF7zrmyfkwFXXV7zu1VNyYKyRVSuFfE5epHRjrJBlfyC_vqwe48Wl7IDCmkMOPx24vNIw0iGGORjA7c2As9R4S_M1IlKcN5a_7Jiy3YepoKxLzo8I2QVPh_Ueg10gJ2ouxvmU6XWZjafOZywLvZn-KHpcYtgGwGlKL8mz0UwJX_3tR_Ltw_uv54fq8fPHT-d3jxUI2eRKdmAZQ9Eh76UUbFDQQa3YODRGqoGpvgPknQVmFW9qJZgcGmzqUaqW9bwVR_Jm1y0mvy_Fj55d2hwYj2FJupZty0QrSjmSfodCDClFHPU9utnEVXOmtxj0Tf8Tg95i0HsMhXveuVj-8sNh1AkcekDrYrmTtsH9h8pvo12bFw</recordid><startdate>202201</startdate><enddate>202201</enddate><creator>Liu, Jiaqi</creator><creator>Gibb, Matthew</creator><creator>Pradhan, Sahar H.</creator><creator>Sayes, Christie M.</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9997-992X</orcidid><orcidid>https://orcid.org/0000-0002-5529-4101</orcidid></search><sort><creationdate>202201</creationdate><title>Synergistic cytotoxicity of bromoacetic acid and three emerging bromophenolic disinfection byproducts against human intestinal and neuronal cells</title><author>Liu, Jiaqi ; Gibb, Matthew ; Pradhan, Sahar H. ; Sayes, Christie M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-57cd00e37e195530b8c7c280fb4a58b0897ce17dc0d81428305b4e42f58609163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Cytotoxicity</topic><topic>DBP</topic><topic>Disinfection byproduct</topic><topic>Interaction</topic><topic>ROS</topic><topic>Synergism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Jiaqi</creatorcontrib><creatorcontrib>Gibb, Matthew</creatorcontrib><creatorcontrib>Pradhan, Sahar H.</creatorcontrib><creatorcontrib>Sayes, Christie M.</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemosphere (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Jiaqi</au><au>Gibb, Matthew</au><au>Pradhan, Sahar H.</au><au>Sayes, Christie M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synergistic cytotoxicity of bromoacetic acid and three emerging bromophenolic disinfection byproducts against human intestinal and neuronal cells</atitle><jtitle>Chemosphere (Oxford)</jtitle><date>2022-01</date><risdate>2022</risdate><volume>287</volume><spage>131794</spage><epage>131794</epage><pages>131794-131794</pages><artnum>131794</artnum><issn>0045-6535</issn><eissn>1879-1298</eissn><abstract>Halogenated disinfection byproducts (halo-DBPs) are drinking water contaminants of great public health concern. Nine haloaliphatic DBPs have been regulated by the U.S. Environmental Protection Agency and various halophenolic compounds have been identified as emerging DBPs. In this study, we evaluated the cytotoxic interactions of the regulated bromoacetic acid and three emerging bromophenolic DBPs, i.e., 2,4,6-tribromophenol, 3,5-dibromo-4-hydroxybenzoic acid, and 3,5-dibromo-4-hydroxybenzaldehyde. Cytotoxicity was measured for each DBP individually as well as each of their mixtures using in vitro human epithelial colorectal adenocarcinoma (Caco-2) and neuroblastoma (SH-SY5Y) cells. Concentration addition (CA) model and isobolographic analysis were employed to characterize the interactions among the DBPs. Our results show that the cytotoxicity of four bromo-DBPs against both cell-types followed the descending rank order of bromoacetic acid &gt; 2,4,6-tribromophenol &gt; 3,5-dibromo-4-hydroxybenzaldehyde &gt; 3,5-dibromo-4-hydroxybenzoic acid. Compared with the toxicity data in literature, our finding that bromoacetic acid showed higher cytotoxicity than bromophenolic DBPs was consistent with the results from Chinese hamster ovary cells (a commonly used in vitro model of DBP toxicological studies); but different from the results obtained from in vivo biological models. Significantly, with CA model prediction, we found that mixtures of four bromo-DBPs exhibited synergistic cytotoxic effects on both human cell types. Isobolographic analysis of binary DBP mixtures revealed that, for Caco-2 cells, bromoacetic acid, 2,4,6-tribromophenol, and 3,5-dibromo-4-hydroxybenzoic acid induced synergism; for SH-SY5Y cells, bromoacetic acid induced synergism with all three bromophenolic DBPs. The production of reactive oxidative species (ROS) induced by DBP mixtures could be an important reason for the synergistic cytotoxicity. [Display omitted] •Bromoacetic acid was more cytotoxic than three bromophenolic DBPs against human cells.•Measured LC50 values of mixtures of the four DBPs were lower than predicted by CA model.•Isobolographic analysis was newly employed to characterize interactions of DBP binary mixtures.•Bromoacetic acid exhibited different degrees of synergistic effects with bromophenolic DBPs.•Production of ROS could be an important reason for the synergism of bromo-DBP mixtures.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.chemosphere.2021.131794</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-9997-992X</orcidid><orcidid>https://orcid.org/0000-0002-5529-4101</orcidid></addata></record>
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subjects Cytotoxicity
DBP
Disinfection byproduct
Interaction
ROS
Synergism
title Synergistic cytotoxicity of bromoacetic acid and three emerging bromophenolic disinfection byproducts against human intestinal and neuronal cells
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