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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (6/6 displayed)

  • 2015Understanding the composition-structure-bioactivity relationships in diopside (CaO center dot MgO center dot 2SiO(2))-tricalcium phosphate (3CaO center dot P2O5) glass system35citations
  • 2012Biocompatibility and biodegradation of polycaprolactone-sebacic acid blended gels63citations
  • 2010Anti-adhesion and antiproliferative cellulose triacetate membrane for prevention of biomaterial-centred infections associated with Staphylococcus epidermidis13citations
  • 2009Osteogenic differentiation of mesenchymal stem cells using PAMAM dendrimers as gene delivery vectors87citations
  • 2006Functionalization of chitosan membranes through phosphorylation: Atomic force microscopy, wettability, and cytotoxicity studies25citations
  • 2001Staphylococcus epidermidis RP62A adhesion to chemically modified cellulose derivatives21citations

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Chart of shared publication
Ferreira, José Maria Da Fonte
1 / 456 shared
Du, Jc
1 / 1 shared
Semitela, Â.
1 / 1 shared
Lourenco, Ah
1 / 1 shared
Xiang, Y.
1 / 7 shared
Sousa, D. M.
1 / 1 shared
Kapoor, S.
1 / 11 shared
Lourenço, A. H.
1 / 1 shared
Semitela, A.
1 / 1 shared
Du, J.
1 / 6 shared
Granja, P. L.
1 / 4 shared
Ferreira, Jmf
1 / 6 shared
Sousa, Dm
1 / 1 shared
Goel, A.
1 / 55 shared
Sanchez, Ems
1 / 1 shared
Salgado, Cl
1 / 3 shared
Zavaglia, Cac
1 / 1 shared
Extremina, Ci
1 / 1 shared
Da Fonseca, Af
1 / 1 shared
Fonseca, Ap
2 / 2 shared
Pego, Ap
1 / 2 shared
Tomas, H.
1 / 10 shared
Santos, Jl
1 / 42 shared
Oramas, E.
1 / 1 shared
Saramago, B.
1 / 2 shared
Melo, Lv
1 / 2 shared
Barbosa, Ma
2 / 6 shared
Amaral, If
1 / 1 shared
Oliveira, Dr
1 / 1 shared
Nogueira, Ja
1 / 1 shared
Chart of publication period
2015
2012
2010
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Co-Authors (by relevance)

  • Ferreira, José Maria Da Fonte
  • Du, Jc
  • Semitela, Â.
  • Lourenco, Ah
  • Xiang, Y.
  • Sousa, D. M.
  • Kapoor, S.
  • Lourenço, A. H.
  • Semitela, A.
  • Du, J.
  • Granja, P. L.
  • Ferreira, Jmf
  • Sousa, Dm
  • Goel, A.
  • Sanchez, Ems
  • Salgado, Cl
  • Zavaglia, Cac
  • Extremina, Ci
  • Da Fonseca, Af
  • Fonseca, Ap
  • Pego, Ap
  • Tomas, H.
  • Santos, Jl
  • Oramas, E.
  • Saramago, B.
  • Melo, Lv
  • Barbosa, Ma
  • Amaral, If
  • Oliveira, Dr
  • Nogueira, Ja
OrganizationsLocationPeople

article

Functionalization of chitosan membranes through phosphorylation: Atomic force microscopy, wettability, and cytotoxicity studies

  • Saramago, B.
  • Melo, Lv
  • Barbosa, Ma
  • Amaral, If
  • Granja, Pl
Abstract

Grafting negatively charged groups such as phosphates is a well-known strategy for inducing the deposition of apatite-like layers under simulated physiological conditions. In this investigation, chitosan was phosphorylated in an attempt to enhance its osteoconduction. Chitosan membranes were phosphorylated at 30 degrees C with the H3PO4/Et3PO4/P2O5/butanol reaction system for periods up to 48 h. This method is an alternative to the phosphoric acid/urea/dimethylformamide phosphorylation method, which involves the use of much higher temperatures. In this study, the effects of the phosphorylation reaction time on the surface morphology and surface free energy of phosphorylated membranes were investigated with atomic force microscopy and static-contact-angle measurements, respectively. In addition, the modified membranes were evaluated with respect to their cytotoxicity toward bone cells through the incubation of human osteoblastic cells with extracts of the materials for two different periods: 24 and 120 h. The results revealed a reduction of the average surface roughness at the nanometer scale with increasing phosphorylation reaction time. Wettability studies showed an increase in the polar component of the surface free energy with increasing reaction time as a result of the increase in the phosphate surface concentration. Cytotoxicity studies revealed no cytotoxic effect of phosphorylated membranes on osteoblastic cells, regardless of the incubation period. (c) 2006 Wiley Periodicals, Inc.

Topics
  • Deposition
  • impedance spectroscopy
  • morphology
  • surface
  • atomic force microscopy
  • functionalization