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This spatial separation strategy substantially increases the loading capacity of both molecules and improves their controlled-release performance, allowing the MTX@COL@MIL-100 capsules to exhibit superior release kinetics for MTX and collagenase under simulated physiological conditions
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Under normoxic conditions, prolyl hydroxylase domain (PHD) enzymes facilitate the hydroxylation of HIF-α subunits, such as HIF-1α
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