AI Article Synopsis

  • Proteases are crucial for wound healing, but in chronic wounds, their excessive activity can hinder recovery by damaging tissue.
  • A new microfluidic chip using multilayered fluorogenic nanofilms has been developed to monitor protease activity with high sensitivity and small sample volume.
  • The chip showed increased fluorescence when exposed to both model proteases and liquid from infected wounds, indicating its potential for real-time monitoring of protease levels during the healing process.

Article Abstract

Proteases play an essential role in the four sequential but overlapping phases of wound healing: hemostasis, inflammation, proliferation, and remodeling. In chronic wounds, excessive protease secretion damages the newly formed extracellular matrix, thereby delaying or preventing the normal healing process. Peptide-based fluorogenic sensors provide a visual platform to sense and analyze protease activity through changes in the fluorescence intensity. Here, we have developed an integrated microfluidic chip coated with multilayered fluorogenic nanofilms that can directly monitor protease activity. Fluorogenic protease sensors were chemically conjugated to polymer films coated on the surface of parallel microfluidic channels. Capillary flow layer-by-layer (CF-LbL) was used for film assembly and combined with subsequent sensor modification to establish a novel platform sensing technology. The benefits of our platform include facile fabrication and processing, controllable film nanostructure, small sample volume, and high sensitivity. We observed increased fluorescence of the LbL nanofilms when they were exposed to model recombinant proteases, confirming their responsiveness to protease activity. Increases in the nanofilms' fluorescence intensity were also observed during incubation with liquid extracted from murine infected wounds, demonstrating the potential of these films to provide real-time, in situ information about protease activity levels.

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Source
http://dx.doi.org/10.1039/d0an01294gDOI Listing

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