4.8 Article

Fabrication of Smart Tantalum Carbide MXene Quantum Dots with Intrinsic Immunomodulatory Properties for Treatment of Allograft Vasculopathy

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 31, Issue 46, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202106786

Keywords

allograft vasculopathy; bioactive material; hydrofluoric acid-free synthesis; in vivo immunomodulation; Ta; C-4; T-3; (x) MXene quantum dots

Funding

  1. Canadian Institutes of Health Research [PJT156148]
  2. CANUSA funding
  3. Canadian Institutes of Health Research fellowship [MEF-171305]

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MXene nanomaterials, particularly Ta4C3Tx MQDs, are gaining interest in interdisciplinary research for addressing medical challenges. These MQDs, leveraging tantalum's anti-inflammatory and antiapoptotic properties, offer a novel nanoplatform for biomedical engineering and show promising results in treating transplant vasculopathy.
MXene nanomaterials have sparked significant interest among interdisciplinary researchers to tackle today's medical challenges. In particular, colloidal MXene quantum dots (MQDs) offer the high specific surface area and compositional flexibility of MXene while providing improvements to aqueous stability and material-cell interactions. The current study for the first time reports the development and application of immunoengineered tantalum-carbide (Ta4C3Tx) MQDs for in vivo treatment of transplant vasculopathy. This report comes at a critical juncture in the field as poor long-term safety of other MXene compositions challenge the eventual clinical translatability of these materials. Using rational design and synthesis strategies, the Ta4C3Tx MQDs leverage the intrinsic anti-inflammatory and antiapoptotic properties of tantalum to provide a novel nanoplatform for biomedical engineering. In particular, these MQDs are synthesized with high efficiency and purity using a facile hydrofluoric acid-free protocol and are enriched with different bioactive functional groups and stable surface TaO2 and Ta2O5. Furthermore, MQDs are spontaneously uptaken into antigen-presenting endothelial cells and alter surface receptor expression to reduce their activation of allogeneic T-lymphocytes. Finally, when applied in vivo, Ta4C3Tx MQDs ameliorate the cellular and structural changes of early allograft vasculopathy. These findings highlight the robust potential of tailored Ta4C3Tx MQDs for future applications in medicine.

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