Thirty milligrams of lyophilized plant were homogenized with 0.75 mL of acidified methanol (HCl 0.1 % v/v), samples were subsequently placed in an ultrasonic bath for 15 min, and then centrifuged at 12.500 rpm for 5 min, and the supernatant was separated from the sediment. Finally, supernatants were pooled and stored at -80 °C until analysis. The entire procedure was carried out in darkness, and the extractions were carried out in triplicate.
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