摘要:
Serving as the primary barrier, skin protects the human body against oxidative stress caused by ultraviolet radiation, pollutants, and free radicals. Antioxidants are essential for preventing oxidative damage. Polyphenols such as ferulic acid (FA) and kaempferol (KMP) demonstrate potent free radical scavenging properties. However, poor solubility, stability, and bioavailability often limit their clinical application. This study aimed to investigate the effect of independent variables (PVA and PLGA concentrations, and sonication time on %EE of payloads, and the particle size (PS) using Box-Behnken design (BBD). PS of the nanoparticles (NPs) ranged from 171.40 ± 2.09 to 212.60 ± 2.37 nm with polydispersity index (PDI) of 0.14–0.287. PS, PDI, and zeta (ζ) potential of the optimized NPs was 189.8 nm, PDI 0.217, and − 11.1 mV, respectively. FE-SEM analysis demonstrated that the NPs were well-dispersed and spherical. Pure FA and KMP showed rapid burst release with 83.15% and 60.52% within 2 h (complete by 4 h), whereas PLGA NPs exhibited sustained biphasic release (FA: 48.00% in 1 h, 81.71% in 6 h, 98.99% in 24 h; KMP: 34.00% in 1 h, 73.83% in 6 h, 98.98% in 24 h). Free FA and KMP showed moderate antioxidant activity with IC50 values of 22.92 ± 3.80 µg/mL and 26.53 ± 2.01 µg/mL, respectively, while the optimized NPs exhibited improved activity with a lower IC50 of 18.69 ± 2.08 µg/mL, compared to ascorbic acid (AA) (4.05 ± 2.98 µg/mL). In the HET-CAM assay, pure FA and KMP showed mild irritation (IS 2.56 and 2.89, respectively), while the optimized NPs were nearly non-irritant (IS 0.52), indicating that encapsulation reduced irritation and improved biocompatibility of payload. The results showed that the NPs prolonged drug release profiles, making them promising delivery carrier. This nanotechnology-driven approach enhances the protective and therapeutic potential of antioxidants in skin care and oxidati