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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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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2018Photocatalytic hydroxyapatite-titania nanocomposites for preventive conservation of marble5citations
  • 2007Biomimetic hydroxyapatite-drug nanocrystals as potential bone substitutes with antitumor drug delivery properties322citations

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Chart of shared publication
Franzoni, Elisa
1 / 3 shared
Damen, Eros
1 / 1 shared
Scherer, George W.
1 / 4 shared
Sassoni, Enrico
1 / 4 shared
Margiotta, Nicola
1 / 3 shared
Mann, Stephen
1 / 25 shared
Walsh, Dominic
1 / 4 shared
Laforgia, Mariarita
1 / 1 shared
Iafisco, Michele
1 / 9 shared
Palazzo, Barbara
1 / 2 shared
Bianchi, Claudia L.
1 / 17 shared
Natile, Giovanni
1 / 1 shared
Chart of publication period
2018
2007

Co-Authors (by relevance)

  • Franzoni, Elisa
  • Damen, Eros
  • Scherer, George W.
  • Sassoni, Enrico
  • Margiotta, Nicola
  • Mann, Stephen
  • Walsh, Dominic
  • Laforgia, Mariarita
  • Iafisco, Michele
  • Palazzo, Barbara
  • Bianchi, Claudia L.
  • Natile, Giovanni
OrganizationsLocationPeople

article

Biomimetic hydroxyapatite-drug nanocrystals as potential bone substitutes with antitumor drug delivery properties

  • Margiotta, Nicola
  • Mann, Stephen
  • Walsh, Dominic
  • Laforgia, Mariarita
  • Iafisco, Michele
  • Palazzo, Barbara
  • Roveri, Norberto
  • Bianchi, Claudia L.
  • Natile, Giovanni
Abstract

This Full Paper investigates the adsorption and desorption of the anticancer drugs cis-diamminedichloroplatinum(II) (CDDP, cisplatin) and the new platinum(II) complex di(ethylenediamineplatinum)medronate (DPM), as well as the clinically relevant bisphosphonate alendronate, towards two biomimetic synthetic HA nanocrystalline materials with either plate-shaped (HAps) or needle-shaped (HAns) morphologies and different chemico-physical properties. The adsorption and desorption kinetics are dependent on the specific properties of the drugs and the morphology of the HA nanoparticles. Adsorption of the platinum complexes occurs with retention of the nitrogen ligands but the chloride ligands of cisplatin are displaced. Despite their opposite charges, the negatively charged alendronate bisphosphonate and the positively charged aquated cisplatin are strongly adsorbed, while the neutral DPM complex shows lower affinity towards the negatively charged apatitic surface. The data suggest that adsorption of the two platinum complexes is driven by electrostatic attractions, while interaction between the alendronate and the HA surface takes place by ligand exchange in which the two phosphonate groups of the drug molecule replace two surface phosphate groups. Significantly, adsorption of positively charged hydrolysis species of cisplatin is more favored on the phosphate-rich HAns surface while adsorption of negatively charged alendronate is more favored on the calcium-rich HAps surface. The latter type of short-range electrostatic interactions also appear to dominate the desorption kinetics; consequently, drug release is greater for neutral DPM than for charged alendronate and aquated cisplatin. Moreover, while the release per unit area of charged species is the same for the two types of HAs, the release of DPM is faster from HAns, which is lower in surface calcium, than for HAps. Overall, this work demonstrates that the properties of HA nanocrystals can be modulated in such a way to produce HA/biomolecule conjugates tailored for ...

Topics
  • nanoparticle
  • impedance spectroscopy
  • surface
  • Platinum
  • Nitrogen
  • Calcium
  • chemical ionisation