FABRICATION AND CHARACTERIZATION OF SILK FIBROIN BASED BIOMATERIALS AS NOVEL WOUND HEALING AGENT IN SKIN TISSUE ENGINEERING
DOI:
https://doi.org/10.22159/ijap.2026v18i4.58008Keywords:
Biomaterial characterization, Composite wound dressing film, Doxycycline-loaded film, In vitro antimicrobial activity, Silk fibroinAbstract
Objective: To develop and optimize a silk fibroin–based composite film incorporating polyvinyl alcohol (PVA), hydroxyethyl cellulose (HEC), hyaluronic acid, and doxycycline, and to evaluate its antibacterial activity for potential in-vitro wound dressing applications.
Methods: Films were prepared using varying concentrations of silk fibroin, PVA, and HEC. A 2³ factorial design was employed to evaluate the individual and interactive effects of silk fibroin (A), PVA (B), and HEC (C) on in-vitro drug release and drug content. The optimized formulation was subjected to physicochemical characterization, including thickness, surface pH, folding endurance, drug content uniformity, and bio-adhesion strength. In-vitro antibacterial activity evaluated against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa. Stability studies were conducted over a period of two months.
Results: Drug release from the formulations ranged from 79.6% to 96.41%, while drug content varied between 85 and 98 mg. PVA significantly enhanced drug release (p = 0.0482), whereas the A×C interaction significantly influenced drug loading (p = 0.0282). The optimized formulation (NS18), containing 0.10 g silk fibroin, 1 g PVA, and 0.05 g HEC, showed 87.16% drug release and 93.12 mg drug content. Films exhibited uniform thickness (0.21–0.26 mm), skin-compatible pH (6.3–6.7), high folding endurance (265–305 folds), strong bio-adhesion (26.9–32.5 g), and pronounced antibacterial activity. Stability studies confirmed minimal changes in drug content and release.
Conclusion: The optimized silk fibroin composite film demonstrated controlled drug release, favourable mechanical and bio-adhesive properties, and effective antimicrobial activity under in-vitro conditions, indicating its potential suitability as a biomaterial for in-vitro wound dressing applications. Further in-vivo and clinical investigations are required to establish its therapeutic efficacy.
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