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Purpose This study aimed at the investigation of the impact of aqueous solubility and dose manipulation on the pharmacokinetics of resveratrol. Methods Water soluble intravenous and oral formulations of resveratrol were prepared with hydroxypropyl-β-cyclodextrin (HP-β-CD) and randomly methylated-β-cyclodextrin (RM-β-CD), respectively. Sodium salt and suspension of resveratrol in carboxymethyl cellulose...
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