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These three AR LBD agonist structures have very similar overall conformations, revealed key ligand and receptor interaction sites, and helped to define the general structural requirements for the binding of ligands in the LBP

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Additionally, the enhanced stability of niosomes compared to other vesicular carriers, due to the chemical stability of non-ionic surfactants against oxidation and hydrolysis, ensures that more of the administered dose reaches the systemic circulation intact [122,123]

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