TY - JOUR
T1 - A novel TCR hydrogel wound dressing loaded with UC-SMC extract enhances skin regeneration and prevents wound scarring
AU - Dai, Wufei
AU - Zhou, Boya
AU - Yi, Bingcheng
AU - Zhang, Wenjie
AU - Zhou, Guangdong
AU - Hua, Yujie
AU - Wang, Wenbo
AU - Liu, Wei
N1 - Publisher Copyright:
© 2023
PY - 2023/6
Y1 - 2023/6
N2 - Tissue fibrosis and scar formation are inevitable parts of wound healing in adult mammals, leading to a range of adverse outcomes including physical disability and psychological problems. In which, inflammation network plays a crucial role in this pathological process. Novel wound dressing materials with ideal biocompatibility, morphology adaptability, adequate mechanical strength, considerable wet-surface adhesion, and active drug delivery properties are urgently needed for clinical applications. In this study, umbilical cord mesenchymal stem cell extract (UC-SCE) was developed and verified for its ability to inhibit wound inflammation by driving macrophage polarization towards the anti-inflammatory (M2) phenotype and to promote wound tissue regeneration in SD rat wound model. Meanwhile, UC-SCE has also been shown to inhibit dermal fibroblast proliferation, migration and matrix production, and also to inhibit angiogenesis both in vitro and in vivo, and thus proving its anti-scarring capability. Furthermore, a novel dynamic-to-covalent hydrogel based on tandem crosslinking reaction (TCR) has been developed as a drug carrier for US-SCE delivery, which demonstrated suitable injectability, proper mechanical stability and excellent tissue adhesion. More importantly, when loaded with UC-SCE, this novel wound dressing was demonstrated able to regenerate wound tissue and inhibit hypertrophic scar formation in a rabbit ear scar model, thus principally proved the feasibility, efficacy and applicability of this novel SCE-hydrogel wound dressing for potential clinical translation.
AB - Tissue fibrosis and scar formation are inevitable parts of wound healing in adult mammals, leading to a range of adverse outcomes including physical disability and psychological problems. In which, inflammation network plays a crucial role in this pathological process. Novel wound dressing materials with ideal biocompatibility, morphology adaptability, adequate mechanical strength, considerable wet-surface adhesion, and active drug delivery properties are urgently needed for clinical applications. In this study, umbilical cord mesenchymal stem cell extract (UC-SCE) was developed and verified for its ability to inhibit wound inflammation by driving macrophage polarization towards the anti-inflammatory (M2) phenotype and to promote wound tissue regeneration in SD rat wound model. Meanwhile, UC-SCE has also been shown to inhibit dermal fibroblast proliferation, migration and matrix production, and also to inhibit angiogenesis both in vitro and in vivo, and thus proving its anti-scarring capability. Furthermore, a novel dynamic-to-covalent hydrogel based on tandem crosslinking reaction (TCR) has been developed as a drug carrier for US-SCE delivery, which demonstrated suitable injectability, proper mechanical stability and excellent tissue adhesion. More importantly, when loaded with UC-SCE, this novel wound dressing was demonstrated able to regenerate wound tissue and inhibit hypertrophic scar formation in a rabbit ear scar model, thus principally proved the feasibility, efficacy and applicability of this novel SCE-hydrogel wound dressing for potential clinical translation.
KW - M2 polarization
KW - Scar inhibition
KW - TCR hydrogel
KW - Umbilical cord stem cell extract
KW - Wound Regeneration
UR - https://www.scopus.com/pages/publications/85150065857
U2 - 10.1016/j.apmt.2023.101785
DO - 10.1016/j.apmt.2023.101785
M3 - 文章
AN - SCOPUS:85150065857
SN - 2352-9407
VL - 32
JO - Applied Materials Today
JF - Applied Materials Today
M1 - 101785
ER -