Post-injury scar-free healing

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Milestone n:0%
What does each milestone mean?

    1 = Clinical need
    2 = Idea
    3 = Proof of concept
    4 = Proof of feasibility
    5 = Proof of value
    6 = Initial clinical trials
    7 = Validation of solution
    8 = Approval and launch
    9 = Clinical use
    10 = Standard of care


The aim of this project is to develop anti-scarring biomembranes for use in cranial surgery and skin wounds. The project team is collaborating with a USA commercial body, Integra, to incorporate an anti-scarring drug, Decorin, into their matrix wound dressing and dural regeneration matrix and then check the release and efficacy of the drug.

Lay Summary

We are trying to enhance the function of dural substitutes for the repair of dural mater and skin wound dressings, which are currently in clinical use, through their incorporation with an anti-scarring drug. This approach will allow us to prevent post-surgical adhesion between the meninges and the overlying skin, which complicates reconstructive surgery and also help scar-free wound healing.


Scars are common, costly and can seriously impair quality of life. In addition to trauma, scarring and fibrosis are associated with broader disease and degenerative conditions. There is no treatment currently proven to control problem fibrosis and lessen the functional impact of scarring.  In the first phase of SRMRC Professors Logan and Grover exploited a potent anti-scarring molecule called Decorin(Esmaeili et al., 2014; Hill et al., 2015). They sourced GMP manufactured recombinant Decorin and demonstrated its translatable potential by securing two fully funded (Wellcome Trust and MRC) clinical trials of our novel formulated anti-scarring dressings to treat skin burns and damaged corneas. We believe this technology has the potential for expansion to other indications to prevent scarring in many more tissues injured by trauma or disease.


The methods we are using in this project including:

  • Production of a prototype of the cranial membrane with a defined formulation approved by clinicians routinely undertaking craniotomy procedures.
  • Assessing the release amount of the drug and its efficacy using ELISA, collagen fibrillogenesis and appropriate models of human meningeal scarring.

Research Team

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