Abstract:The antioxidant and whitening activities of pearl shell peptides were systematically evaluated using combined cellular and animal model systems to further elucidate their bioactive potential. The HepG2 cell model was employed to assess cellular antioxidant capacity and protection against oxidative damage, while a D-galactose-induced Drosophila melanogaster model was utilized to examine oxidative stress modulation. Additionally, the inhibitory effects on melanogenesis were investigated using both B16F10 mouse melanoma cells and zebrafish models. Significant intracellular antioxidant activity (EC50=0.163 mg·mL-1) was demonstrated, with 0.2 mg·mL-1 pearl shell peptides shown to restore viability of damaged cells from 80.99% to 96.55% (P<0.05). In D-galactose-treated Drosophila, remarkable enhancements were observed in superoxide dismutase (SOD) and catalase (CAT) activities (P<0.05), accompanied by reduced malondialdehyde (MDA) content. For whitening effects, melanin content and tyrosinase activity in B16F10 cells were significantly decreased by 26.47% and 29.79%, respectively, at 0.05 mg·mL-1. Corresponding reductions of 32.33% and 56.72% were recorded in zebrafish. The peptide profile was characterized by mass spectrometry, with identified sequences exhibiting strong correlation with bioactivity assessments. These findings collectively establish that pearl shell peptides possess dual antioxidant-whitening functionalities at both cellular and organismal levels. Collectively, pearl shell peptides were demonstrated to exhibit potent antioxidant and whitening activities across cellular and organismal models, establishing a scientific basis for their potential application as skin-health promoting nutraceutical ingredients.