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Updated: Dec 7, 2025

Use of the Protease Fluorescent Detection Kit to Determine Protease Activity
Published on: August 4, 2009
Fluorimetric ex vivo quantification of protease debriding efficacy on natural substrate
Reddy Sreekanth Vootukuri1,2, Mike P Philpott1, Giuseppe Trigiante1
1Blizard Institute, Centre for Cell Biology and Cutaneous Research, Queen Mary University of London, London, UK.
Abstract:
Debridement is the process of removal of necrotic and infected tissue to clean a wound or burn and expedite healing. Proteases such as papain, bromelain, and collagenase that promote debridement by degrading proteins in the dead tissue are in use today. However, the only method to measure debriding efficacy in vitro is the fluorescent monitoring of the digestion of an Artificial Wound Eschar (AWE) substrate. This AWE substrate contains a pellet of only three eschar matrix proteins collagen, elastin, and fibrin which do not account for the complexity and the composition of necrotic tissue. Here, we describe an ex vivo method using dry necrotic full thickness human skin and ortho-phthalaldehyde (OPA), a molecule commonly used for sensitive fluorimetric protein detection to monitor debridement activity. We advocate this simple yet sensitive approach to detect debridement efficacy that can readily be used commercially to benchmark products prior to in vivo testing.

