Biocompatible tailored zirconia mesoporous nanoparticles with high surface area for theranostic applications.

J Mater Chem B

Department of Molecular Sciences and Nanosystems, Centro di Microscopia Elettronica "Giovanni Stevanato" and INSTM, Università Ca' Foscari Venezia, via Torino 155/b, 30170 Venezia-Mestre, Italy.

Published: September 2015

AI Article Synopsis

  • Nanocarriers, specifically mesoporous zirconia nanoparticles (MZNs), are gaining attention in nanomedicine for their potential theranostic applications.
  • A new method using neutral surfactants, alkali halides, and vacuum extraction has been developed to create MZNs with a significantly higher surface area compared to existing techniques.
  • Biological tests confirm that these MZNs are biocompatible, cell-permeable, and degradable, supporting their use in therapeutic and diagnostic applications.

Article Abstract

Nanocarriers as theranostic agents are under the spotlight in modern nanomedicine, and mesoporous nanomaterials represent a class of devices of major interest. Zirconia is biocompatible, inert with good mechanical and thermal properties for in vivo biomedical applications. Although a few examples of zirconia nanoparticles have been described, a major limitation was the low surface area, which is fundamental for payload transport. Here, a simple and highly efficient method is described for the synthesis of spherical mesoporous zirconia nanoparticles (MZNs) with a high surface area through a neutral surfactant-assisted sol-gel method. The combination of alkali halides and vacuum extraction allowed stabilization of the shape and size of MZNs and to avoid porous network failure, respectively. In comparison to published synthesis procedures, a high surface area has been obtained. Biological experiments demonstrated that MZNs were biocompatible, cell permeable and degradable providing a proof of concept for theranostic applications. A comparison with the properties of mesoporous silica nanoparticles has also been performed.

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Source
http://dx.doi.org/10.1039/c5tb01424gDOI Listing

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