Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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693.932 PEOPLE
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Show results for 693.932 people that are selected by your search filters.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2024Surfactant-Dependent Bulk Scale Mechanochemical Synthesis of CsPbBr3 Nanocrystals for Plastic Scintillator-Based X-ray Imaging13citations
  • 2023Hydrothermal and Mechanosynthesis of Mixed-Cation Double Perovskite Scintillators for Radiation Detectioncitations
  • 2015Controlling colloidal stability of silica nanoparticles during bioconjugation reactions with proteins and improving their longer-term stability, handling and storage45citations

Places of action

Chart of shared publication
Anaya Martín, Miguel
1 / 2 shared
Salway, H.
2 / 2 shared
Wolfe, D.
2 / 2 shared
Masteghin, M. G.
1 / 1 shared
Ghosh, J.
2 / 2 shared
Dorey, R.
2 / 3 shared
Braddock, I.
2 / 2 shared
Sellin, P.
2 / 5 shared
Oneill, J.
2 / 4 shared
Reiss, J.
2 / 3 shared
Richards, S.
1 / 4 shared
Alghamdi, S.
1 / 1 shared
Anaya, M.
1 / 9 shared
Mulholland, R.
1 / 1 shared
Wilson, M.
1 / 12 shared
Gubala, V.
1 / 6 shared
Okennedy, Richard
1 / 1 shared
Nogués, C.
1 / 17 shared
Montón, H.
1 / 1 shared
Williams, D. E.
1 / 8 shared
Moore, C. J.
1 / 1 shared
Chart of publication period
2024
2023
2015

Co-Authors (by relevance)

  • Anaya Martín, Miguel
  • Salway, H.
  • Wolfe, D.
  • Masteghin, M. G.
  • Ghosh, J.
  • Dorey, R.
  • Braddock, I.
  • Sellin, P.
  • Oneill, J.
  • Reiss, J.
  • Richards, S.
  • Alghamdi, S.
  • Anaya, M.
  • Mulholland, R.
  • Wilson, M.
  • Gubala, V.
  • Okennedy, Richard
  • Nogués, C.
  • Montón, H.
  • Williams, D. E.
  • Moore, C. J.
OrganizationsLocationPeople

article

Controlling colloidal stability of silica nanoparticles during bioconjugation reactions with proteins and improving their longer-term stability, handling and storage

  • Gubala, V.
  • Okennedy, Richard
  • Nogués, C.
  • Montón, H.
  • Crean, C.
  • Williams, D. E.
  • Moore, C. J.
Abstract

© The Royal Society of Chemistry 2015. Despite the potential of antibody-coated nanoparticles (Ab-NPs) in many biological applications, there are very few successful, commercially available examples in which the carefully engineered nanomaterial has made it beyond the laboratory bench. Herein we explore the robustness and cost of protein-nanoparticle conjugation. Using multivalent polyamidoamine (PAMAM) dendrimers and dextran as crosslinkers, it was possible to retain colloidal stability during (i) NP-linker binding and (ii) the subsequent conjugation reaction between linker-coated NPs and proteins to generate monodisperse Ab-NPs. This was attributed to the physicochemical properties of the linkers, which were inherited by the NPs and thus benefited colloidal stability. Attaching negatively charged, EDC/sulfo-NHS-activated PAMAM to the NPs contributed to overall negative charge of particles, and in turn led to high electrostatic attraction between the protein and PAMAM-coated NPs during the reaction conditions. In contrast, using an uncharged, EDC/NHS-activated PAMAM dendrimer led to NP aggregation and lower protein binding efficiency. Dextran as a cost-effective, uncharged macromolecule allowed for steric repulsions between neighbouring particles during protein binding, thus inducing NP stability in solution, and also produced monodisperse Ab-NPs. By freeze-drying Ab-NPs from a 1% BSA solution it is possible to reconstitute the solid-form colloid back to a stable state by adding solvent and simply shaking the sample vial by hand. The consequences of the different surface chemistries and freeze-drying stabilizers on the colloidal stability of the NPs were probed by dynamic light scattering. The performance of Ab-NPs was compared in a simple fluorescence linked immunoassay in whole serum. Interestingly, the signal-to-noise ratios were similar for Ab-NPs using PAMAM and dextran, despite dextran binding fewer Abs per NP. We believe this work provides researchers with the tools and strategies for reliably generating Ab-NPs that can be used for a variety of biological applications. This journal is

Topics
  • nanoparticle
  • impedance spectroscopy
  • surface
  • dendrimer
  • drying
  • dynamic light scattering