TY - JOUR
T1 - Chitosan-Based Membranes for Skin Wound Repair in a Dorsal Fold Chamber Rat Model
AU - Casimiro, Maria Helena
AU - Ferreira, Luís M.
AU - Santos, Pedro M.P.
AU - Leal, João P.
AU - Rodrigues, Gabriela
AU - Iria, Inês
AU - Alves, Sara
AU - Pais, Diogo
AU - Casal, Diogo
N1 - Funding Information:
This research was funded by the International Atomic Energy Agency under Research Contract No. 18202 (CRP F23030). Authors acknowledge FCT—Fundação para a Ciência e a Tecnologia I.P. for the national funds in the scope of the project UIDB/04349/2020+UIDP/04349/2020, UIDB/00100/2020 and UIDB/00329/2020.
Publisher Copyright:
© 2022 by the authors.
PY - 2022/12
Y1 - 2022/12
N2 - Frequently, deep partial and full-thickness skin wounds do not spontaneously regenerate. To restore the normal function of skin, epidermal and dermal components have to be supplied to the wound bed by grafting various substrates. Available options are limited and frequently costly. Herein, authors present a possible approach using 3D skin scaffolds capable of mimicking structure and biological functions of the extracellular matrix, providing, in parallel, a good environment for cell attachment, proliferation and differentiation. Low-molecular weight chitosan-based membranes were prepared by freeze-drying and ionizing radiation techniques to be used as skin scaffolds. Poly (vinyl alcohol), PVA, vinyl pyrrolidone, VP, and gelatin from cold water fish were incorporated. Information regarding membranes’ physical-chemical properties from SEM analysis, swelling and weight loss, together with biological response through in vitro assays (using Human Caucasian Fetal Foreskin Fibroblast) allowed the selection of an optimized batch of membranes that was used as skin scaffold in a dorsal rat model wound. The in vivo implantation assays (in Wistar rats) resulted in very promising results: (i) healing process faster than control; (ii) good vascularization; (iii) viable new tissues morphologically functional.
AB - Frequently, deep partial and full-thickness skin wounds do not spontaneously regenerate. To restore the normal function of skin, epidermal and dermal components have to be supplied to the wound bed by grafting various substrates. Available options are limited and frequently costly. Herein, authors present a possible approach using 3D skin scaffolds capable of mimicking structure and biological functions of the extracellular matrix, providing, in parallel, a good environment for cell attachment, proliferation and differentiation. Low-molecular weight chitosan-based membranes were prepared by freeze-drying and ionizing radiation techniques to be used as skin scaffolds. Poly (vinyl alcohol), PVA, vinyl pyrrolidone, VP, and gelatin from cold water fish were incorporated. Information regarding membranes’ physical-chemical properties from SEM analysis, swelling and weight loss, together with biological response through in vitro assays (using Human Caucasian Fetal Foreskin Fibroblast) allowed the selection of an optimized batch of membranes that was used as skin scaffold in a dorsal rat model wound. The in vivo implantation assays (in Wistar rats) resulted in very promising results: (i) healing process faster than control; (ii) good vascularization; (iii) viable new tissues morphologically functional.
KW - cell proliferation
KW - chitosan
KW - gamma radiation
KW - gelatin
KW - PVA
KW - regenerative medicine
KW - skin scaffolds
KW - VP
UR - http://www.scopus.com/inward/record.url?scp=85144860017&partnerID=8YFLogxK
U2 - 10.3390/pharmaceutics14122736
DO - 10.3390/pharmaceutics14122736
M3 - Article
C2 - 36559232
AN - SCOPUS:85144860017
VL - 14
JO - Ionic Liquids and Deep Eutectic Solvents for Application in Pharmaceutics
JF - Ionic Liquids and Deep Eutectic Solvents for Application in Pharmaceutics
SN - 1999-4923
IS - 12
M1 - 2736
ER -