AI Article Synopsis

  • * A new method called perfusion decellularization creates a scaffold from porcine fasciocutaneous flaps that preserves essential properties such as collagen, microvasculature, and growth factors, making it a promising alternative to traditional flaps.
  • * The study found that using 0.2% sodium dodecyl sulfate effectively clears cellular material from the flap while maintaining its structure, indicating biocompatibility as human dermal fibroblasts were able to migrate into the decellularized tissue.

Article Abstract

Reconstructive techniques to repair severe tissue defects include the use of autologous fasciocutaneous flaps, which may be limited due to donor site availability or lead to complications such as donor site morbidity. A number of synthetic or natural dermal substitutes are in use clinically, but none have the architectural complexity needed to reconstruct deep tissue defects. The perfusion decellularization of fasciocutaneous flaps is an emerging technique that yields a scaffold with the necessary composition and vascular microarchitecture and serves as an alternative to autologous flaps. In this study, we show the perfusion decellularization of porcine fasciocutaneous flaps using sodium dodecyl sulfate (SDS) at three different concentrations, and identify that 0.2% SDS results in a decellularized flap that is efficiently cleared of its cellular material at 86%, has maintained its collagen and glycosaminoglycan content, and preserved its microvasculature architecture. We further demonstrate that the decellularized graft has the porous structure and growth factors that would facilitate repopulation with cells. Finally, we show the biocompatibility of the decellularized flap using human dermal fibroblasts, with cells migrating as deep as 150 µm into the tissue over a 7-day culture period. Overall, our results demonstrate the promise of decellularized porcine flaps as an interesting alternative for reconstructing complex soft tissue defects, circumventing the limitations of autologous skin flaps.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11047669PMC
http://dx.doi.org/10.3390/bioengineering11040321DOI Listing

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