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Each sample was then split into two fraction (100 μL) and treated as follows: For H 2 S measurement, 100 μL of each sample was precipitated with 1 mL of absolute MeOH at –40 °C for 2 h, centrifuged (16,000 × g at 0 °C), and obtained supernatant was evaporated and the residue was resuspended and sonicated in 100 μL of 50 mM HEPES buffer (pH 7.4)

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D’autres recherches et essais cliniques seront nécessaires pour valider l’innocuité et l’efficacité de ces formulations, mais la perspective de gouttes ophtalmiques à base d’antioxydants représente une avenue prometteuse pour de futures thérapies oculaires