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High-throughput preparation of hexagonally ordered mesoporous silica and gadolinosilicate nanoparticles for use as MRI contrast agents

journal contribution
posted on 2024-11-01, 09:00 authored by N.M.K. Tse, D.F. Kennedy, B.A, Moffat, N Kirby, Rachel CarusoRachel Caruso, Calum DrummondCalum Drummond
The development of biomedical nanoparticulate materials for use in diagnostics is a delicate balance between performance, particle size, shape, and stability. To identify materials that satisfy all of the criteria it is useful to employ automated high-throughput (HT) techniques for the study of these materials. The structure and performance of surfactant templated mesoporous silica is very sensitive to a wide number of variables. Variables, such as the concentration of the structure-directing agent, the cosolvent and dopant ions and also the temperature and concentration of quenching all have an influence on the structure, surface chemistry, and therefore, the performance of the mesoporous silica nanoparticles generated. Using an automated robotic synthetic platform, a technique has been developed for the high-throughput preparation of mesoporous silica and gadolinium-doped silicate (gadoliniosilicate) nanoparticulate MRI contrast agents. Twelve identical repeats of both the mesoporous silica and gadolinosilicate were synthesized to investigate the reproducibility of the HT technique. Very good reproducibility in the production of the mesoporous silica and the gadolinosilcate materials was obtained using the developed method. The performance of the gadolinosilicate materials was comparable as a T 1 agent to the commercial MRI contrast agents. This HT methodology is highly reproducible and an effective tool that can be translated to the discovery of any sol-gel derived nanomaterial.

History

Related Materials

  1. 1.
    DOI - Is published in 10.1021/co300035q
  2. 2.
    ISSN - Is published in 15204774

Journal

ACS Combinatorial Science

Volume

14

Issue

8

Start page

443

End page

450

Total pages

8

Publisher

American Chemical Society

Place published

United States

Language

English

Copyright

© 2012 American Chemical Society

Former Identifier

2006044215

Esploro creation date

2020-06-22

Fedora creation date

2015-01-16