Literature DB >> 26472246

Pulmonary toxicity of indium-tin oxide production facility particles in rats.

Melissa A Badding1, Natalie R Fix1, Marlene S Orandle1, Mark W Barger1, Katherine M Dunnick1, Kristin J Cummings2, Stephen S Leonard1.   

Abstract

Indium-tin oxide (ITO) is used to make transparent conductive coatings for touch-screen and liquid crystal display electronics. Occupational exposures to potentially toxic particles generated during ITO production have increased in recent years as the demand for consumer electronics continues to rise. Previous studies have demonstrated cytotoxicity in vitro and animal models have shown pulmonary inflammation and injury in response to various indium-containing particles. In humans, pulmonary alveolar proteinosis (PAP) and fibrotic interstitial lung disease have been observed in ITO facility workers. However, which indium materials or specific processes in the workplace may be the most toxic to workers is unknown. Here we examined the pulmonary toxicity of three different particle samples that represent real-life worker exposures, as they were collected at various production stages throughout an ITO facility. Indium oxide (In2O3), sintered ITO (SITO) and ventilation dust (VD) particles each caused pulmonary inflammation and damage in rats over a time course (1, 7 and 90 days post-intratracheal instillation), but SITO and VD appeared to induce greater toxicity in rat lungs than In2O3 at a dose of 1 mg per rat. Downstream pathological changes such as PAP and fibrosis were observed in response to all three particles 90 days after treatment, with a trend towards greatest severity in animals exposed to VD when comparing animals that received the same dose. These findings may inform workplace exposure reduction efforts and provide a better understanding of the pathogenesis of an emerging occupational health issue. Published 2015. This article is a U.S. Government work and is in the public domain in the USA.

Entities:  

Keywords:  cytokines; indium-tin oxide; occupational exposure; phagocytosis; pulmonary toxicity

Mesh:

Substances:

Year:  2015        PMID: 26472246      PMCID: PMC4752405          DOI: 10.1002/jat.3253

Source DB:  PubMed          Journal:  J Appl Toxicol        ISSN: 0260-437X            Impact factor:   3.446


  31 in total

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3.  Pulmonary toxicity in mice by 2- and 13-week inhalation exposures to indium-tin oxide and indium oxide aerosols.

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4.  Pulmonary alveolar proteinosis in workers at an indium processing facility.

Authors:  Kristin J Cummings; Walter E Donat; David B Ettensohn; Victor L Roggli; Peter Ingram; Kathleen Kreiss
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