In Vitro Toxicity Assessment of Emitted Materials Collected During the Manufacture of Water Pipe Plastic Linings
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2019/03/21
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Description:Objectives: US water infrastructure is in need of widespread repair due to age-related deterioration. Currently, the cured-in-place (CIPP) procedure is the most common method for water pipe repair. This method involves the on-site manufacture of a new polymer composite plastic liner within the damaged pipe. The CIPP process can release materials resulting in occupational and public health concerns. To understand hazards associated with CIPP-related emission exposures, an in vitro toxicity assessment was performed. Materials and Methods: Mouse alveolar epithelial and alveolar macrophage cell lines and condensates collected at 3 worksites utilizing styrene-based resins were utilized for evaluations. All condensate samples were normalized based on the major emission component, styrene. Further, a styreneonly exposure group was used as a control to determine mixture related toxicity. Results: Cytotoxicity differences were observed between worksite samples, with the CIPP worksite 4 sample inducing the most cell death. A proteomic evaluation was performed, which demonstrated styrene-, worksite-, and cell-specific alterations. This examination of protein expression changes determined potential biomarkers of exposure including transglutaminase 2, advillin, collagen type 1, perilipin- 2, and others. Pathway analysis of exposure-induced proteomic alterations identified MYC and p53 to be regulators of cellular responses. Protein changes were also related to pathways involved in cell damage, immune response, and cancer. Conclusions: Together these findings demonstrate potential risks associated with the CIPP procedure as well as variations between worksites regarding emissions and toxicity. Our evaluation identified biological pathways that require a future evaluation and also demonstrates that exposure assessment of CIPP worksites should examine multiple chemical components beyond styrene, as many cellular responses were styrene-independent. [Description provided by NIOSH]
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ISSN:0895-8378
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Pages in Document:131-146
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Volume:31
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Issue:4
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NIOSHTIC Number:nn:20057911
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Citation:Inhal Toxicol 2019 Mar; 31(4):131-146
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Contact Point Address:Jonathan Shannahan, School of Health Sciences, College of Human and Health Sciences, Purdue University, 550 Stadium Mall Drive, West Lafayette, IN 47907, USA
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Email:jshannah@purdue.edu
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CAS Registry Number:
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Federal Fiscal Year:2019
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Performing Organization:University of Illinois at Chicago
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Peer Reviewed:True
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Start Date:20050701
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Source Full Name:Inhalation Toxicology
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End Date:20290630
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Main Document Checksum:urn:sha-512:d4ff84a209c0cb5a7e9c53e3596bd8abc0c8d2d32c1dc344f1217593e040e56e913f21561a6de0553c32ede1f2773808936318ed17a843af2b1f54e95e6c206c
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