4.5 Article

Incorporating a structural extracellular matrix gradient into a porcine urinary bladder matrix-based hydrogel dermal scaffold

Journal

JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A
Volume 109, Issue 10, Pages 1893-1904

Publisher

WILEY
DOI: 10.1002/jbm.a.37181

Keywords

chronic wounds; extracellular matrix; hydrogel; scaffold; tissue engineering

Funding

  1. NIBIB/NIH Center for Engineering Complex Tissues [P41EB023833]
  2. NSF CBET [5246870]

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The study investigates a graded-concentration hydrogel composed of porcine urinary bladder matrix (UBM) for potential chronic wound treatment, showing stability, cellular activity, and resistance to fibroblast-mediated contraction. The gradient hydrogel maintained cross-sectional area during degradation and supported high surface cell viability, leveraging the unique advantages of high and low-concentration ECM hydrogels.
The increasing prevalence of chronic, nonhealing wounds necessitates the investigation of full-thickness skin substitutes conducive to host integration and wound closure. Extracellular matrix (ECM)-based hydrogel scaffolds mimic the physiological matrix environment of dermal cells, thereby conferring favorable cellular adhesion, infiltration, and proliferation. However, low-concentration ECM hydrogels rapidly lose mechanical strength as they degrade, leaving them susceptible to shrinkage from fibroblast-mediated contraction. Conversely, high-concentration ECM hydrogels are typically too dense to permit nutrient diffusion and cellular migration. This study investigates the design and fabrication of a graded-concentration hydrogel composed of porcine urinary bladder matrix (UBM) as a dermal scaffold for potential use in chronic wound treatment. Our method of UBM isolation and decellularization effectively removed native DNA while preserving matrix proteins. Hydrogels composed of a range of decellularized UBM (dUBM) concentrations were characterized and used to design a three-tiered gradient hydrogel that promoted cellular activity and maintained structural integrity. The gradient dUBM hydrogel showed stability of cross-sectional area during collagenase degradation, despite considerable loss of mass. The gradient dUBM hydrogel also resisted fibroblast-mediated contraction while supporting high surface cell viability, demonstrating the mechanical support provided by denser layers of dUBM. Overall, incorporation of an ECM concentration gradient into a porcine UBM-based hydrogel scaffold capitalizes on the unique advantages of both high and low-concentration ECM hydrogels, and mitigates the structural weaknesses that have limited the efficacy of hydrogel dermal scaffolds for chronic wounds. Our gradient design shows promise for future development of stable, pro-regenerative wound scaffolds with customized architectures using 3D printing.

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