TY - JOUR
T1 - Engineering a bacterial polysaccharide-based metal-organic framework-enhanced bioactive 3D hydrogel for accelerated full-thickness wound healing
AU - Dan, Aniruddha
AU - Panigrahi, Ankita
AU - Singh, Hemant
AU - Murali, Varsha
AU - Meena, Manisha
AU - Goyel, Prateek
AU - Karthikeyan, Laxmanan
AU - Misra, Superb K.
AU - Varghese, Nibu
AU - Babu, Sharlene Sara
AU - Dalvi, Yogesh B.
AU - Dhanka, Mukesh
N1 - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY - 2025
Y1 - 2025
N2 - Hydrogels offer numerous advantages in wound healing, making them a promising alternative to traditional wound dressings. Their biocompatibility and high water content closely resemble natural biological tissues, creating a moist environment that accelerates cell proliferation and tissue repair. Hydrogels maintain optimal hydration levels, preventing wound desiccation and promoting faster healing. Furthermore, their ability to incorporate and deliver therapeutic agents such as antibiotics, anti-inflammatory drugs, or growth factors provides a multifunctional platform for enhanced wound care. Despite these advantages, current clinical wound-dressing materials often fall short in addressing the complexities of wound healing. Hydrogels, with their customizable properties and potential for integration with emerging technologies, represent a significant opportunity to overcome these limitations and improve clinical outcomes in wound management. Herein, we developed a multi-functional Cu-MOF and tannic acid-enriched polymeric hydrogel dressing composed of gellan-gum/zein for full-thickness wound repair. The physical interactions, including electrostatic interaction and hydrogen bonding between the hydrogel components, form a stable hydrogel matrix. The hydrogel exhibits antioxidant properties and antibacterial activity, and is hemocompatible and biocompatible against L929 fibroblast cells. Furthermore, the fabricated hydrogel dressing improvised a full-thickness wound-healing process in rats. Only 1.6% of the wound area was remaining in the case of GG-Z-TA/M1-treated full-thickness wounds in rats. Histopathology images suggest the Cu-MOF-loaded hydrogels aided in extensive re-epithelialization, neovascularization, and hair follicle formation to accelerate the wound-healing process.
AB - Hydrogels offer numerous advantages in wound healing, making them a promising alternative to traditional wound dressings. Their biocompatibility and high water content closely resemble natural biological tissues, creating a moist environment that accelerates cell proliferation and tissue repair. Hydrogels maintain optimal hydration levels, preventing wound desiccation and promoting faster healing. Furthermore, their ability to incorporate and deliver therapeutic agents such as antibiotics, anti-inflammatory drugs, or growth factors provides a multifunctional platform for enhanced wound care. Despite these advantages, current clinical wound-dressing materials often fall short in addressing the complexities of wound healing. Hydrogels, with their customizable properties and potential for integration with emerging technologies, represent a significant opportunity to overcome these limitations and improve clinical outcomes in wound management. Herein, we developed a multi-functional Cu-MOF and tannic acid-enriched polymeric hydrogel dressing composed of gellan-gum/zein for full-thickness wound repair. The physical interactions, including electrostatic interaction and hydrogen bonding between the hydrogel components, form a stable hydrogel matrix. The hydrogel exhibits antioxidant properties and antibacterial activity, and is hemocompatible and biocompatible against L929 fibroblast cells. Furthermore, the fabricated hydrogel dressing improvised a full-thickness wound-healing process in rats. Only 1.6% of the wound area was remaining in the case of GG-Z-TA/M1-treated full-thickness wounds in rats. Histopathology images suggest the Cu-MOF-loaded hydrogels aided in extensive re-epithelialization, neovascularization, and hair follicle formation to accelerate the wound-healing process.
UR - https://www.scopus.com/pages/publications/105006640875
U2 - 10.1039/d5bm00133a
DO - 10.1039/d5bm00133a
M3 - Article
C2 - 40433815
AN - SCOPUS:105006640875
SN - 2047-4830
JO - Biomaterials Science
JF - Biomaterials Science
ER -