Post-Electrospinning Surface Functionalization of PCL Nanofibrous Membranes with Sisal Extracts: Extract-Dependent Cytocompatibility and Bioactivity

Chronic wounds are frequently associated with persistent inflammation, motivating the development of biofunctional materials capable of modulating cellular responses. In this proof-of-concept study, electrospun poly(ε-caprolactone) (PCL) nanomembranes were surface-functionalized by post-electrospinning drop coating with extracts derived from Agave sisalana agroindustrial residue obtained through two distinct routes: a saponin-rich fraction (EDP) and an acid-hydrolyzed sapogenin-enriched fraction (EAH). The study aimed to investigate how the extract phytochemical profile influences cytocompatibility and bioactivity when incorporated onto electrospun platforms. Phytochemical analysis revealed high total saponin content in EDP (33.83 ± 2.93 g/100 g) and significant sapogenin content in EAH (11.56 ± 0.60 g/100 g). SEM and FTIR-ATR analyses confirmed preservation of the fibrous architecture and polymer backbone, indicating predominantly physical surface incorporation. Biological evaluation demonstrated extract-dependent responses: PCL+EDP 5% exhibited marked cytotoxicity, consistent with the known membrane-disruptive properties of glycosylated saponins, whereas PCL+EAH 5% maintained high cell viability and showed anti-inflammatory activity (75% inhibition of phagocytosis; 56% protection against hemolysis) along with enhanced fibroblast migration (100% wound closure at 72 h). These findings highlight the critical role of extract chemical composition in determining the biological performance of surface-functionalized nanofibrous systems and support sapogenin-enriched fractions as safer bioactive modifiers for electrospun biomaterial platforms.