TY - JOUR
T1 - Chitosan-based hydrogels
T2 - Revolutionizing corneal wound healing with antibacterial and regenerative properties
AU - Hussain, Md Sadique
AU - Alfawaz Altamimi, Abdulmalik Saleh
AU - Afzal, Muhammad
AU - Babu, M. Arockia
AU - Goyal, Kavita
AU - R, Roopashree
AU - Kaur, Irwanjot
AU - Kumar, Sachin
AU - Kumar, M. Ravi
AU - Ali, Haider
AU - Gupta, Gaurav
AU - Balaraman, Ashok Kumar
N1 - Publisher Copyright:
© 2025 Elsevier Ltd
PY - 2025/9
Y1 - 2025/9
N2 - Corneal injuries and infections pose a serious threat to vision. However, conventional therapies topical antibiotics, synthetic grafts, and bandage contact lenses often fail to provide enduring antimicrobial defense and robust tissue regeneration. Researchers derive chitosan-based hydrogels from deacetylated chitin, combining intrinsic polycationic antimicrobial efficacy with tunable biodegradation and excellent biocompatibility, thereby addressing both challenges simultaneously. These hydrogels exert broad-spectrum infection control by disrupting bacterial membranes, chelating essential metal ions and amplifying adjunctive agents such as antibiotics or silver nanoparticles against Pseudomonas aeruginosa and Staphylococcus aureus. Optimized fabrication through physical crosslinking (electrostatic interactions, metal-ion coordination, hydrophobic associations) and covalent strategies (photoinitiated or radiation-induced polymerization) yields scaffolds that withstand eyelid shear forces without compromising corneal transparency. In vitro evaluations show that human corneal epithelial cells and keratocytes remain over 95 % viable, while in vivo alkali-burn studies in rabbits and rats reveal rapid re-epithelialization, stromal remodeling, and nerve regeneration with minimal inflammation. Beyond structural support, chitosan hydrogels actively sculpt the healing microenvironment by scavenging reactive oxygen species, down-regulating pro-inflammatory cytokines, and enabling thermosresponsive release of bioactive factors such as stromal cell–derived factor-1α, ferulic acid, and exosomes, by addressing translational hurdles including sterilization without loss of bioactivity, reproducible manufacturing, regulatory compliance for ophthalmic biomaterials and synchronization of degradation kinetics with healing timelines. This review integrates molecular insights, fabrication strategies and in vivo performance data to inform the rational design of optimized chitosan hydrogel formulations for next-generation ocular therapeutics.
AB - Corneal injuries and infections pose a serious threat to vision. However, conventional therapies topical antibiotics, synthetic grafts, and bandage contact lenses often fail to provide enduring antimicrobial defense and robust tissue regeneration. Researchers derive chitosan-based hydrogels from deacetylated chitin, combining intrinsic polycationic antimicrobial efficacy with tunable biodegradation and excellent biocompatibility, thereby addressing both challenges simultaneously. These hydrogels exert broad-spectrum infection control by disrupting bacterial membranes, chelating essential metal ions and amplifying adjunctive agents such as antibiotics or silver nanoparticles against Pseudomonas aeruginosa and Staphylococcus aureus. Optimized fabrication through physical crosslinking (electrostatic interactions, metal-ion coordination, hydrophobic associations) and covalent strategies (photoinitiated or radiation-induced polymerization) yields scaffolds that withstand eyelid shear forces without compromising corneal transparency. In vitro evaluations show that human corneal epithelial cells and keratocytes remain over 95 % viable, while in vivo alkali-burn studies in rabbits and rats reveal rapid re-epithelialization, stromal remodeling, and nerve regeneration with minimal inflammation. Beyond structural support, chitosan hydrogels actively sculpt the healing microenvironment by scavenging reactive oxygen species, down-regulating pro-inflammatory cytokines, and enabling thermosresponsive release of bioactive factors such as stromal cell–derived factor-1α, ferulic acid, and exosomes, by addressing translational hurdles including sterilization without loss of bioactivity, reproducible manufacturing, regulatory compliance for ophthalmic biomaterials and synchronization of degradation kinetics with healing timelines. This review integrates molecular insights, fabrication strategies and in vivo performance data to inform the rational design of optimized chitosan hydrogel formulations for next-generation ocular therapeutics.
KW - Antibacterial
KW - Biocompatibility
KW - Hydrogel fabrication
KW - Ocular applications
KW - Regenerative biomaterials
KW - Tissue regeneration
UR - https://www.scopus.com/pages/publications/105009283885
U2 - 10.1016/j.exer.2025.110503
DO - 10.1016/j.exer.2025.110503
M3 - Review article
C2 - 40588092
AN - SCOPUS:105009283885
SN - 0014-4835
VL - 258
JO - Experimental Eye Research
JF - Experimental Eye Research
M1 - 110503
ER -