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Moreover, bD-G1A and tD-G1A exhibited improved in vitro Caco-2 cellular permeability and showed higher in vivo bioavailability (7.58% and 8.63%) after oral administration
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“Incretin-based therapies, including agonists of the [glucagon-like peptide 1] and [glucose-dependent insulinotropic polypeptide] receptors, have been
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