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 (7/7 displayed)

  • 2019Co-electrospraying of tumour cell mimicking hollow polymeric microspheres for diffusion magnetic resonance imaging13citations
  • 2015Mechanical properties of porous ceramic scaffolds: Influence of internal dimensions201citations
  • 2015Mechanical properties of porous ceramic scaffolds: Influence of internal dimensions:Influence of Internal Dimensions201citations
  • 2014Enzymatically triggered peptide hydrogels for 3D cell encapsulation and culture41citations
  • 2012Gel-cast glass-ceramic tissue scaffolds of controlled architecture produced via stereolithography of moulds27citations
  • 2011Mechanosensitive peptide gelation: Mode of agitation controls mechanical properties and nano-scale morphology72citations
  • 2009Introducing chemical functionality in Fmoc-peptide gels for cell culture286citations

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Chart of shared publication
Cristinacce, Penny Hubbard
1 / 3 shared
Parker, Geoff
1 / 4 shared
Zhou, Fenglei
1 / 3 shared
Wimpenny, Ian
1 / 4 shared
Wu, Hui Hui
1 / 2 shared
Zhang, Xun
1 / 12 shared
Mchugh, Damien
1 / 3 shared
Derby, Brian
3 / 45 shared
Sabree, Israa
2 / 2 shared
Guilbaud, Jean-Baptiste
1 / 2 shared
Szkolar, Laura
1 / 1 shared
Saiani, Alberto
2 / 9 shared
Miller, Aline F.
1 / 5 shared
Chopra, K.
1 / 1 shared
Mummery, Pm
1 / 20 shared
De Leonardis, Piero
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Helen, Wilda
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Ulijn, Rein V.
2 / 8 shared
Tirelli, Nicola
1 / 13 shared
Richardson, Stephen M.
1 / 6 shared
Hodson, Nigel
1 / 7 shared
Hirst, Andrew R.
1 / 1 shared
Jayawarna, Vineetha
1 / 2 shared
Chart of publication period
2019
2015
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2009

Co-Authors (by relevance)

  • Cristinacce, Penny Hubbard
  • Parker, Geoff
  • Zhou, Fenglei
  • Wimpenny, Ian
  • Wu, Hui Hui
  • Zhang, Xun
  • Mchugh, Damien
  • Derby, Brian
  • Sabree, Israa
  • Guilbaud, Jean-Baptiste
  • Szkolar, Laura
  • Saiani, Alberto
  • Miller, Aline F.
  • Chopra, K.
  • Mummery, Pm
  • De Leonardis, Piero
  • Helen, Wilda
  • Ulijn, Rein V.
  • Tirelli, Nicola
  • Richardson, Stephen M.
  • Hodson, Nigel
  • Hirst, Andrew R.
  • Jayawarna, Vineetha
OrganizationsLocationPeople

article

Introducing chemical functionality in Fmoc-peptide gels for cell culture

  • Richardson, Stephen M.
  • Hodson, Nigel
  • Gough, Julie
  • Ulijn, Rein V.
  • Hirst, Andrew R.
  • Saiani, Alberto
  • Jayawarna, Vineetha
Abstract

Aromatic short peptide derivatives, i.e. peptides modified with aromatic groups such as 9-fluorenylmethoxycarbonyl (Fmoc), can self-assemble into self-supporting hydrogels. These hydrogels have some similarities to extracellular matrices due to their high hydration, relative stiffness and nanofibrous architecture. We previously demonstrated that Fmoc-diphenylalanine (Fmoc-F2) provides a suitable matrix for two-dimensional (2D) or three-dimensional (3D) culture of primary bovine chondrocytes. In this paper we investigate whether the introduction of chemical functionality, such as NH2, COOH or OH, enhances compatibility with different cell types. A series of hydrogel compositions consisting of combinations of Fmoc-F2 and n-protected Fmoc amino acids, lysine (K, with side chain R = (CH2)4NH2), glutamic acid (D, with side chain R = CH2COOH), and serine (S, with side chain R = CH2OH) were studied. All compositions produced fibrous scaffolds with fibre diameters in the range of 32-65 nm as assessed by cryo-scanning electron microscopy and atomic force microscopy. Fourier transform infrared spectroscopy analysis suggested that peptide segments adopt a predominantly antiparallel β-sheet conformation. Oscillatory rheology results show that all four hydrogels have mechanical profiles of soft viscoelastic materials with elastic moduli dependent on the chemical composition, ranging from 502 Pa (Fmoc-F2/D) to 21.2 KPa (Fmoc-F2). All gels supported the viability of bovine chondrocytes as assessed by a live-dead staining assay. Fmoc-F2/S and Fmoc-F2/D hydrogels in addition supported viability for human dermal fibroblasts (HDF) while Fmoc-F2/S hydrogel was the only gel type that supported viability for all three cell types tested. Fmoc-F2/S was therefore investigated further by studying cell proliferation, cytoskeletal organization and histological analysis in 2D culture. In addition, the Fmoc-F2/S gel was shown to support retention of cell morphology in 3D culture of bovine chondrocytes. These results demonstrate that introduction of chemical functionality into Fmoc-peptide scaffolds may provide gels with tunable chemical and mechanical properties for in vitro cell culture. © 2009 Acta Materialia Inc.

Topics
  • scanning electron microscopy
  • atomic force microscopy
  • chemical composition
  • two-dimensional
  • Fourier transform infrared spectroscopy