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

Places of action

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
2009
2006
2001

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

Biocompatibility and biodegradation of polycaprolactone-sebacic acid blended gels

  • Sanchez, Ems
  • Salgado, Cl
  • Granja, Pl
  • Zavaglia, Cac
Abstract

Tissue engineering aims at creating biological body parts as an alternative for transplanting tissues and organs. A current new approach for such materials consists in injectable biodegradable polymers. Their major advantages are the ability to fill-in defects, easy incorporation of therapeutic agents or cells, and the possibility of minimal invasive surgical procedures. Polycaprolactone (PCL) is a promising biodegradable and elastic biomaterial, with the drawback of low-degradation kinetics in vivo. In this work a biodegradable injectable gel of PCL blended with sebacic acid (SA) was prepared, to improve the degradation rate of the biomaterial. SA is known for its high degradation rate, although in high concentrations it could originate a pH decrease and thus disturb the biocompatibility of PCL. Degradation tests on phosphate buffered saline were carried out using 5% of SA on the blend and the biomaterial stability was evaluated after degradation using differential scanning calorimetry, dynamical mechanical analysis, and scanning electronic microscopy. After degradation the elastic properties of the blend decreased and the material became more crystalline and stiffer, although at a lower extent when compared with pure PCL. The blend also degraded faster with a loss of the crystalline phase on the beginning (30 days), although its thermal and mechanical properties remained comparable with those of the pure material, thus showing that it achieved the intended objectives. After cell assays the PCL-SA gel was shown to be cytocompatible and capable of maintaining high cell viability (over 90%). (C) 2011 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 100A: 243-251, 2012.

Topics
  • impedance spectroscopy
  • polymer
  • crystalline phase
  • defect
  • differential scanning calorimetry
  • biocompatibility
  • microscopy