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[0022] A major hurdle in nasal delivery is the rapid removal of drug formulations (aqueous solution or dry powder) from the nasal cavity by rapid mucociliary beating, resulting in a clearance half-life of about 15 min for ordinary formulations, as well as low bioavailability (Merkus et al., 1998), especially for semaglutide and other polypeptides with high molecular mass and low diffusion rate across mucosal epithelium

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The No DAC variant lacks the Drug Affinity Complex modification