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Cytotoxicity and immunomodulatory effects of sol-gel combustion based titanium dioxide (TiO2) particles of large surface area on RAW 264.7 macrophages
The current study was designed to investigate the cytotoxicity and immunomodulatory effects of sol-gel combustion based TiO2 particles (glycine and l-alanine as reducing agents) of large surface area on RAW 264.7 macrophages. RAW 264.7 macrophages exposed to varying concentrations of TiO2 particles...
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Published in: | Toxicology in vitro 2017-09, Vol.43, p.92-103 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The current study was designed to investigate the cytotoxicity and immunomodulatory effects of sol-gel combustion based TiO2 particles (glycine and l-alanine as reducing agents) of large surface area on RAW 264.7 macrophages. RAW 264.7 macrophages exposed to varying concentrations of TiO2 particles (0.001 to 1000μg/ml) were assessed after 24h and showed a reduced cell viability at 100 and 1000μg/ml and increased LDH release at 10μg/ml. Furthermore, TiO2 particles (0.1, 1 and 10μg/ml) were utilized to assess the immune responses and intracellular ROS levels on RAW 264.7 macrophages. TiO2 particles at 10μg/ml showed increased mRNA expression of inflammatory cytokines (TNFα, IL-1β and IL-6), inflammatory mediators (iNOS and COX-2) and transcription factor (NFκB) similar to that of LPS stimulated macrophages. However, the mRNA expression levels were found near normal levels at lower concentrations (0.1 and 1μg/ml). In addition, TiO2 particles at 10μg/ml also increased the production of inflammatory cytokines (TNFα, IL-1β and IL-6) and intracellular ROS levels in RAW 264.7 macrophages similar to that of LPS stimulated macrophages. Conclusively, TiO2 particles prepared through this method at a concentration≤0.1μg/ml can be used for various biological applications with minimal immunomodulatory effects.
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•Sol-gel combustion based TiO2 particles (glycine and l-alanine as reducing agents).•In vitro cytotoxicity analysis of TiO2 particles of large surface area.•Immune responses of low concentrations of TiO2 particles.•ROS levels of cells exposed to TiO2 particles. |
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ISSN: | 0887-2333 1879-3177 |
DOI: | 10.1016/j.tiv.2017.06.006 |