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Short-term inhalation study of graphene oxide nanoplates.

TLDR
Similar to previously reported graphene inhalation data, this short-term nose-only inhalation study found only minimal or unnoticeable graphene oxide toxicity in the lungs and other organs.
Abstract
Graphene oxides possess unique physicochemical properties with important potential applications in electronics, pharmaceuticals, and medicine. However, the toxicity following inhalation exposure to graphene oxide has not yet been clarified. Therefore, this study conducted a short-term graphene oxide inhalation toxicity analysis using a nose-only inhalation exposure system and male Sprague-Dawley rats. A total of four groups (15 rats per group) were exposed: (1) control (fresh air), (2) low concentration (0.76 ± 0.16 mg/m3), (3) moderate concentration (2.60 ± 0.19 mg/m3), and (4) high concentration (9.78 ± 0.29 mg/m3). The rats were exposed to graphene oxide for 6 h/day for 5 days, followed by recovery for 1, 3, and 21 days. No significant body or organ weight changes were noted after the short-term exposure or during the recovery period. Similarly, no significant systemic effects of toxicological importance were noted in the hematological assays, bronchoalveolar lavage fluid (BAL) inflammatory markers, BAL fluid cytokines, or blood biochemical assays following the graphene oxide exposure or during the post-exposure observation period. Moreover, no significant differences were observed in the BAL cell differentials, such as lymphocytes, macrophages, or polymorphonuclear cells. Graphene oxide-ingested alveolar macrophages as a spontaneous clearance reaction were observed in the lungs of all the concentration groups from post 1 day to post 21 days. Histopathological examination of the liver and kidneys did not reveal any significant test-article-relevant histopathological lesions. Importantly, similar to previously reported graphene inhalation data, this short-term nose-only inhalation study found only minimal or unnoticeable graphene oxide toxicity in the lungs and other organs.

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A Review on Graphene-Based Nanomaterials in Biomedical Applications and Risks in Environment and Health

TL;DR: The history, synthesis, structural properties and recent developments of GBNs for biomedical applications, as well as GBNs applications in tissue engineering and in research as biosensors and bioimaging materials, are examined.
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Characterization of M1 and M2 polarization phenotypes in peritoneal macrophages after treatment with graphene oxide nanosheets

TL;DR: FITC-PEG-GO uptake did not induce the macrophage polarization towards the M1 pro-inflammatory phenotype, promoting the control of the M 1/M2 balance with a slight shift towards M2 reparative phenotype involved in tissue repair, ensuring an appropriate immune response to these nanosheets.
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Size‐Dependent Pulmonary Impact of Thin Graphene Oxide Sheets in Mice: Toward Safe‐by‐Design

TL;DR: It is suggested that airborne exposure to micrometer‐sized GO should be avoided in the production plant or applications, where aerosolized dispersions are likely to occur, and the findings demonstrate that lateral dimensions play a fundamental role in the pulmonary response to GO.
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A transcriptomic overview of lung and liver changes one day after pulmonary exposure to graphene and graphene oxide

TL;DR: The differences in transcriptomic responses between the two GBM types can be used to understand how physicochemical properties influence biological response and enable hazard evaluation of GBM and hazard ranking of GO and rGO, both in relation to each other and to other nanomaterials.
References
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Journal ArticleDOI

Biological Interactions of Graphene-Family Nanomaterials: An Interdisciplinary Review

TL;DR: A systematic nomenclature for this set of Graphene-Family Nanomaterials (GFNs) is proposed and specific materials properties relevant for biomolecular and cellular interactions are discussed and several unique modes of interaction between GFNs and nucleic acids, lipid bilayers, and conjugated small molecule drugs and dyes are discussed.
Journal ArticleDOI

In vitro toxicity evaluation of graphene oxide on A549 cells

TL;DR: In this article, a comprehensive study on the toxicity of graphene oxide (GO) by examining the influences of GO on the morphology, viability, mortality and membrane integrity of A549 cells was performed.
Journal ArticleDOI

A Graphene Oxide–Organic Dye Ionic Complex with DNA‐Sensing and Optical‐Limiting Properties

TL;DR: Graphene oxide, a nonstoichiometric, two-dimensionalbonsheet resulting fromacidexfoliation ofgraphite, offers a new class of solution-dispersible polyaromatic platform for performing chemistry.
Journal ArticleDOI

Organic Radical-Assisted Electrochemical Exfoliation for the Scalable Production of High-Quality Graphene

TL;DR: A novel method based on the controlled electrochemical exfoliation of graphite in aqueous ammonium sulfate electrolyte to produce graphene in large quantities and with outstanding quality, offering great promise for the preparation of graphene that can be utilized in industrial applications to create integrated nanocomposites, conductive or mechanical additives, as well as energy storage and conversion devices.
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Is graphene oxide hazardous?

Importantly, similar to previously reported graphene inhalation data, this short-term nose-only inhalation study found only minimal or unnoticeable graphene oxide toxicity in the lungs and other organs.