O1. Obtaining and structural characterization of the components (collagen and pyrrole-sulfonamide hybrids) needed for proposed formulas.
O2. In vitro evaluation of the cyto/hemocompatibility, antimicrobial, antibiofilm, antioxidant, immunomodulatory and pro-wound healing effects for both individual constituents and designed collagen-based formulas.
O3. The optimization and verification of compositional consistency for the formulas exhibiting the most promising biological activity.
O4. Project management and dissemination.
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