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Attenuation of protease activity in chronic wound fluid with bisphosphonate-functionalised hydrogels.

Abstract
Chronic ulcers are an important and costly medical issue, imposing considerable pain, reduced mobility and decreased quality of life. The common pathology in these chronic wounds is excessive proteolytic activity, resulting in degradation of key factors critical to the ulcer's ability to heal. Matrix metalloproteinases (MMPs), a large family of zinc-dependent endopeptidases, have been shown to have increased activity in chronic wound fluid (CWF), with many authors suggesting that they need to be inhibited for the ulcer to heal. The studies we report here show that the excessive MMP activity in CWF can be inhibited with the bisphosphonate alendronate, in the form of a sodium salt, a functionalised analogue, and tethered to a poly(2-hydroxy methacrylate) (PHEMA) hydrogel. Furthermore, these functionalised alendronate hydrogels appear to be biologically inert as assessed in a three-dimensional ex vivo human skin equivalent model. Together, these results highlight the potential use of a tethered MMP inhibitor to inhibit protease activity in wound fluid. This approach may improve wound healing as it still allows MMPs to remain active in the upper cellular layers of the ulcer bed where they perform vital roles in wound healing; thus may offer an attractive new device-orientated wound therapy.
AuthorsErin A Rayment, Tim R Dargaville, Gary K Shooter, Graeme A George, Zee Upton
JournalBiomaterials (Biomaterials) Vol. 29 Issue 12 Pg. 1785-95 (Apr 2008) ISSN: 0142-9612 [Print] Netherlands
PMID18241915 (Publication Type: Journal Article)
Chemical References
  • Diphosphonates
  • Drug Carriers
  • Hydrogels
  • Matrix Metalloproteinase Inhibitors
Topics
  • Body Fluids (metabolism)
  • Diphosphonates (administration & dosage, chemistry)
  • Drug Carriers (chemistry)
  • Enzyme Activation (drug effects)
  • Humans
  • Hydrogels (chemistry)
  • Materials Testing
  • Matrix Metalloproteinase Inhibitors
  • Ulcer (drug therapy, enzymology)
  • Wound Healing (drug effects)

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