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P-value 0.01 (*)
We equally divided thirty-six male Wistar albino rats into three groups: the group of rats without any treatment (control group), the group of rats treated with deep-frying oil of 0.42 ml/rat/day (negative control group), and the group of rats co-treated with deep-frying oil of 0.42 ml/rat/day and L-Carnitine of 30 mg/kg/day (treatment group)
Samples were prepared with TA (30, 150, and 300 g/mL) [26], EDTA (100, 500, and 1000 g/mL) [27], and AA (10, 50, and 100 g/mL) [28] due to their applications in reducing oxidation and scavenging free radicals in both ophthalmic and non-ophthalmic settings
article/abs/pii/S0146280624000422 Drucker, D
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