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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University of Strathclyde

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2023Characterisation of native and decellularised porcine tendon under tension and compression2citations
  • 2023A chaos-inspired biomechanical biomarker of ankle instabilitycitations
  • 2016Paradoxical size effects in composite laminates and other heterogeneous materials1citations
  • 2015The effects of decellularisation on the mechanical properties of bone, and subsequent recellularisation of the samples.citations
  • 2014Characterisation and Validation of Sawbones™ Artificial Composite Femur materialcitations
  • 2013On the Poisson's ratio of the nucleus pulposus11citations
  • 2012Assessment of forces imparted on seating systems by children with special needs during daily living activities1citations

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Chart of shared publication
Fermor, Hazel L.
1 / 1 shared
Edwards, Jennifer H.
1 / 1 shared
Solis-Cordova, Jacqueline
1 / 1 shared
Herbert, Anthony
1 / 1 shared
Brockett, Claire L.
1 / 1 shared
Forsyth, Lauren
1 / 2 shared
Mulder, Kim
1 / 1 shared
Hickey, Matthew
1 / 1 shared
Fleming, Grace
1 / 1 shared
Ligeti, Alexandra
1 / 1 shared
Frame, Jamie C.
1 / 1 shared
Wheel, Marcus
2 / 2 shared
Grant, Mary
1 / 2 shared
Mohamad, M. Mohd Riduan Bin
1 / 1 shared
Young, A. M.
1 / 2 shared
Gilroy, Daniel
1 / 1 shared
Phillips, A.
1 / 3 shared
Farrell, Mark
1 / 2 shared
Green, Peter
1 / 1 shared
Lees, Karl
1 / 1 shared
Samaneein, Katika
1 / 1 shared
Chart of publication period
2023
2016
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2012

Co-Authors (by relevance)

  • Fermor, Hazel L.
  • Edwards, Jennifer H.
  • Solis-Cordova, Jacqueline
  • Herbert, Anthony
  • Brockett, Claire L.
  • Forsyth, Lauren
  • Mulder, Kim
  • Hickey, Matthew
  • Fleming, Grace
  • Ligeti, Alexandra
  • Frame, Jamie C.
  • Wheel, Marcus
  • Grant, Mary
  • Mohamad, M. Mohd Riduan Bin
  • Young, A. M.
  • Gilroy, Daniel
  • Phillips, A.
  • Farrell, Mark
  • Green, Peter
  • Lees, Karl
  • Samaneein, Katika
OrganizationsLocationPeople

article

Characterisation of native and decellularised porcine tendon under tension and compression

  • Fermor, Hazel L.
  • Edwards, Jennifer H.
  • Solis-Cordova, Jacqueline
  • Riches, Philip
  • Herbert, Anthony
  • Brockett, Claire L.
Abstract

Decellularised porcine superflexor tendon (pSFT) has been characterised as a suitable scaffold for anterior cruciate ligament replacement, with dimensions similar to hamstring tendon autograft. However, decellularisation of tissues may reduce or damage extracellular matrix components, leading to undesirable biomechanical changes at a whole tissue scale.Although the role of collagen in tendons is well established, the mechanical contribution of glycosaminoglycans (GAGs) is less evident and could be altered by the decellularisation process. In this study, the contribution of GAGs to the tensile and compressive mechanical properties of pSFT was determined and whether decellularisation affected these properties by reducing GAG content or functionality.<br/><br/>PSFTs were either enzymatically treated using chondroitinase ABC to remove GAGs or decellularised using previously established methods. Native, GAG-depleted and decellularised pSFT groups were then subjected to quantitative assays and biomechanical characterisation. In tension, specimens underwent stress relaxation and strength testing. In compression, specimens underwent confined compression testing. <br/><br/>The GAG-depleted group was found to have a significantly lower GAG content than native and decellularised groups. There was no significant difference in GAG content between native and decellularised groups.Although stress relaxation testing discovered a reduction in the time-independent relaxation modulus in the decellularised group, there were no other significant differences between any of the groups for any of the remaining parameters assessed with stress relaxation or strength testing in tension. In compression testing, the aggregate modulus was found to be significantly lower in the GAG-depleted group than the native and decellularised groups, while the permeability was significantly higher in the GAG-depleted group than the decellularised group.<br/><br/>The results indicate that GAGs significantly contribute to the mechanical properties of pSFT in compression, but not in tension. Furthermore, the content and function of GAGs in pSFTs are unaffected by decellularisation and the mechanical properties of the tissue are retained.<br/>

Topics
  • impedance spectroscopy
  • laser emission spectroscopy
  • strength
  • permeability