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3a), the * transition of pterin ring at 282 nm and the saddle point at 360 nm of FA were observed in FA-rGO, suggesting the conjugation of FA to rGO 56

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Mechanistically, they activate Nrf2 and block ubiquitin-mediated GPX4 degradation, thereby inhibiting ferroptosis and alleviating cartilage erosion, pain, and gait abnormalities in DMM-induced OA (192)