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Open Access Review Issue
Titanium Dioxide Nanoparticle and Cardiovascular Diseases: A Critical Review of the Literature and Possible Underlying Mechanisms
Nano Biomedicine and Engineering 2022, 14 (4): 329-342
Published: 31 December 2022
Downloads:171
Background

Over the last decades, the exposure to titanium dioxide nanoparticles (TiO2 NPs) has increased due to the wide application in industry, food adduct, medicine, cosmetic products, etc. Literature review showed that the TiO2 NPs exert toxic effects on several organs.

Methods

We searched PubMed, MEDLINE and the other databases with the following keywords, "titanium dioxide nanoparticle", "TiO2 NPs", "myocardial infarction", "endothelial", "blood pressure", "heart" and "cardiovascular", and reviewed the literature by focusing on the toxic effects of TiO2 NPs on the cardiovascular system, and possible underlying mechanism.

Results

The toxic effects of TiO2 NPs on the cardiovascular system are controversial but some possible mechanisms were proposed. TiO2 NPs and nanoparticle-derived titanium induce cardiac injury, endothelial dysfunction and increase blood pressure and heart rate. These effects are mediated via systemic or local oxidative stress and inflammation.

Conclusion

The TiO2 NPs toxicity is dependent on cell type and particle characteristic, and the controversial results may be due to these variables. However, a growing body of evidence confirmed the possible TiO2 NPs toxicity on the cardiovascular system.

Open Access Letter to the Editor Issue
The Role of Glucose Transporter 1 in Drug Delivery: Transporter, Receptor and/or Signaling Component
Nano Biomedicine and Engineering 2019, 11 (4): 347-350
Published: 14 November 2019
Downloads:17

The targeting of cell surface molecules is a promising strategy in drug delivery. Glucose modified-nanocarrier interacts with glucose transporter 1 (GLUT1) as a target molecule and increases nanocarrier-drug internalization to cancer and brain endothelial cells. The mechanism by which GLUT1 promotes nanocarrier internalization remains unclear. Herein, we propose that the interaction of GLUT1 and nanocarrier absorbs and traps the nanocarrier and simultaneously activates cell signaling pathways that is responsible for activation of the endocytosis system.

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