EVALUATION OF THE EFFECTIVENESS OF THE APPLICATION OF ACELLULAR DERMAL MATRIX IN THE HEALING OF FULL-THICKNESS WOUNDS: COMBINED MORPHOLOGICAL AND THERMOMETRIC ANALYSIS IN PIGS
DOI:
https://doi.org/10.11603/1811-2471.2026.v.i2.16403Keywords:
аcellular dermal matrix, extracellular matrix scaffold, full-thickness wound model, wound healing, infrared thermography, granulation tissue, angiogenesis, bone tissueAbstract
SUMMARY. The extracellular matrix (ECM) plays a fundamental role in tissue regeneration by providing structural support and regulating cell migration, proliferation, and differentiation during wound healing. In full-thickness skin injuries, extensive destruction of the native ECM disrupts these processes and delays tissue repair. Acellular dermal matrix (ADM) has emerged as a promising biomaterial capable of reproducing the structural and functional characteristics of the native ECM and promoting regenerative processes in damaged tissues.
The aim – to evaluate the morphological and thermometric indicators of the effectiveness of acellular dermal matrix in the healing of full-thickness skin wounds using an experimental porcine model.
Material and Methods. Full-thickness skin wounds (5 × 5 cm) were created on the dorsal surface of a pig. Two experimental groups were formed: control wounds treated with non-adhesive dressings and wounds covered with ADM. The healing process was assessed on days 3, 7, 14, and 21. Histological examination of punch biopsy specimens stained with hematoxylin and eosin was performed to evaluate inflammatory response, granulation tissue formation, and epithelialization. Infrared thermography was used to monitor temperature dynamics in the wound area.
Results. Histological analysis demonstrated that ADM application was associated with reduced neutrophilic inflammation, earlier fibroblast and vascular ingrowth, and more organized granulation tissue formation. By day 14, wounds treated with ADM showed advanced epithelialization with formation of a multilayered epithelium, whereas control wounds exhibited only partial epithelial coverage. By day 21, ADM-treated wounds demonstrated near-complete epithelialization and structural integration of the matrix within newly formed connective tissue. Thermographic analysis revealed phase-dependent temperature dynamics corresponding to different stages of wound healing and reflecting the modulatory effect of ADM on inflammatory activity and angiogenesis.
Conclusions. The use of acellular dermal matrix promotes more regulated wound healing by attenuating acute inflammation, facilitating angiogenesis, and accelerating epithelialization. Combined morphological and infrared thermographic assessment represents a valuable approach for monitoring wound healing dynamics and evaluating the therapeutic efficacy of regenerative biomaterials.
References
Diller RB, Tabor AJ. The role of the extracellular matrix (ECM) in wound healing: a review. Biomimetics (Basel). 2022;7(3):87. DOI: 10.3390/biomimetics7030087. DOI: https://doi.org/10.3390/biomimetics7030087
Chiu A, Jia W, Sun Y, et al. Fibroblast-generated extracellular matrix guides anastomosis during wound healing in an engineered lymphatic skin flap. Bioengineering (Basel). 2023;10(2):149. DOI: 10.3390/bioengineering10020149. DOI: https://doi.org/10.3390/bioengineering10020149
Harmon KA, Burnette MD, Avery JT, et al. Varying properties of extracellular matrix grafts impact their durability and cell attachment and proliferation in an in vitro chronic wound model. J Tissue Eng Regen Med. 2024;2024:6632276. DOI: 10.1155/2024/6632276. DOI: https://doi.org/10.1155/2024/6632276
Da LC, Huang YZ, Xie HQ, et al. Membranous extracellular matrix-based scaffolds for skin wound healing. Pharmaceutics. 2021;13(11):1796. DOI: 10.3390/pharmaceutics13111796. DOI: https://doi.org/10.3390/pharmaceutics13111796
Marinkovic M, Sridharan R, Santarella F, et al. Optimization of extracellular matrix production from human induced pluripotent stem cell-derived fibroblasts for scaffold fabrication for application in wound healing. J Biomed Mater Res A. 2021;109:1803-11. DOI: 10.1002/jbm.a.37173. DOI: https://doi.org/10.1002/jbm.a.37173
Li G, Shen Q, Zhou P, et al. Acellular dermal matrix for one-stage treatment of lower extremity full-thickness skin defect: a case series. BMC Surg. 2023;23:17. DOI: 10.1186/s12893-022-01871-x. DOI: https://doi.org/10.1186/s12893-022-01871-x
Boháč M, Danišovič Ľ, Koller J, et al. What happens to an acellular dermal matrix after implantation in the human body? A histological and electron microscopic study. Eur J Histochem. 2018;62(1):2873. DOI: 10.4081/ejh.2018.2873. DOI: https://doi.org/10.4081/ejh.2018.2873
Campitiello F, Mancone M, Cammarota M, et al. Acellular dermal matrix used in diabetic foot ulcers: clinical outcomes supported by biochemical and histological analyses. Int J Mol Sci. 2021;22(13):7085. DOI:10.3390/ijms22137085. DOI: https://doi.org/10.3390/ijms22137085
Ramirez-Garcia Luna JL, Bartlett R, Arriaga-Caballero JE, et al. Infrared thermography in wound care, surgery, and sports medicine: a review. Front Physiol. 2022;13:838528. DOI:10.3389/fphys.2022.838528. DOI: https://doi.org/10.3389/fphys.2022.838528
Fridberg M, Bafor A, Iobst CA, et al. The role of thermography in assessment of wounds: a scoping review. Injury. 2024;55(11):111833. DOI: 10.1016/j.injury.2024. 111833. DOI: https://doi.org/10.1016/j.injury.2024.111833
Kulianda O. Experimental modelling of full-thickness skin wounds in pigs. Bull Med Biol Res. 2025;7(1):43-50. DOI: 10.61751/bmbr/1.2025.43. DOI: https://doi.org/10.63341/bmbr/1.2025.43
Schindelin J, Arganda-Carreras I, Frise E, et al. Fiji: an open-source platform for biological-image analysis. Nat Methods. 2012;9(7):676-82. DOI: 10.1038/nmeth.2019. DOI: https://doi.org/10.1038/nmeth.2019
Dai C, Shih S, Khachemoune A. Skin substitutes for acute and chronic wound healing: an updated review. J Dermatolog Treat. 2020;31(6):639-48. DOI: 10.1080/ 09546634.2018.1530443. DOI: https://doi.org/10.1080/09546634.2018.1530443
Zhang Y, Chen ZH, Zhao K, et al. Acellular embryoid body and hydroxybutyl chitosan composite hydrogels promote M2 macrophage polarization and accelerate diabetic cutaneous wound healing. Mater Today Bio. 2024; 25:100975. DOI: 10.1016/j.mtbio.2024.100975. DOI: https://doi.org/10.1016/j.mtbio.2024.100975
He C, Yang Z, Jin Y, et al. ADM scaffolds generate a pro-regenerative microenvironment during full-thickness cutaneous wound healing through M2 macrophage polarization via Lamtor1. Front Physiol. 2018;9:657. DOI: 10.3389/fphys.2018.00657. DOI: https://doi.org/10.3389/fphys.2018.00657
He T, Xiao Y, Guo Z, et al. Modulation of macrophage function by bioactive wound dressings with an emphasis on extracellular matrix-based scaffolds and nanofibrous composites. Pharmaceutics. 2023;15(3):794. DOI: 10.3390/pharmaceutics15030794. DOI: https://doi.org/10.3390/pharmaceutics15030794
Paganelli A, Naselli AG, Bertoni L, et al. Wound healing after acellular dermal substitute positioning in dermato-oncological surgery: a prospective comparative study. Life (Basel). 2023;13(2):463. DOI: 10.3390/life13020463. DOI: https://doi.org/10.3390/life13020463
Liang R, Pan R, He L, et al. Decellularized extracellular matrices for skin wound treatment. Materials (Basel). 2025;18(12):2752. DOI: 10.3390/ma18122752. DOI: https://doi.org/10.3390/ma18122752